<?xml version='1.0' encoding='UTF-8'?><?xml-stylesheet href="http://www.blogger.com/styles/atom.css" type="text/css"?><feed xmlns='http://www.w3.org/2005/Atom' xmlns:openSearch='http://a9.com/-/spec/opensearchrss/1.0/' xmlns:blogger='http://schemas.google.com/blogger/2008' xmlns:georss='http://www.georss.org/georss' xmlns:gd="http://schemas.google.com/g/2005" xmlns:thr='http://purl.org/syndication/thread/1.0'><id>tag:blogger.com,1999:blog-7775904593195892177</id><updated>2024-11-01T03:33:10.831-07:00</updated><title type='text'>Naphthoquinones</title><subtitle type='html'>this blog dedicated to Quinone, Naphthoquinone, 2,3-dichloro-1,4-naphthoquinone, dichlone, Juglone etc organic compound</subtitle><link rel='http://schemas.google.com/g/2005#feed' type='application/atom+xml' href='http://naphthoquinone.blogspot.com/feeds/posts/default'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/7775904593195892177/posts/default?redirect=false'/><link rel='alternate' type='text/html' href='http://naphthoquinone.blogspot.com/'/><link rel='hub' href='http://pubsubhubbub.appspot.com/'/><author><name>Hardesh</name><uri>http://www.blogger.com/profile/15195689814375098224</uri><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='https://img1.blogblog.com/img/b16-rounded.gif'/></author><generator version='7.00' uri='http://www.blogger.com'>Blogger</generator><openSearch:totalResults>1</openSearch:totalResults><openSearch:startIndex>1</openSearch:startIndex><openSearch:itemsPerPage>25</openSearch:itemsPerPage><entry><id>tag:blogger.com,1999:blog-7775904593195892177.post-4944739417997742979</id><published>2011-09-19T10:49:00.000-07:00</published><updated>2011-10-13T10:39:33.380-07:00</updated><title type='text'>2,3-Dichloro-1,4-naphthoquinone</title><content type='html'>&lt;div dir=&quot;ltr&quot; style=&quot;text-align: left;&quot; trbidi=&quot;on&quot;&gt;
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&lt;span class=&quot;Apple-style-span&quot; style=&quot;color: white;&quot;&gt;Does euphonious remind you of an attachment&lt;/span&gt;&lt;br /&gt;
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&lt;ol start=&quot;1&quot; style=&quot;text-align: left;&quot; type=&quot;1&quot;&gt;
 &lt;ul type=&quot;disc&quot;&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-family: Arial;&quot;&gt;&amp;nbsp;&amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN&quot;&gt;1,4-Naphthalenedione,
      2,3-dichloro- &lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/b&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;1,4-Naphthoquinone,
      2,3-dichloro- &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;2,
      3-Dichloro-.alpha.-naphthoquinone &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;2, 3-Dichloronaphthoquinone
      &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;2,3-Dichlor-1,4-naftochinon
      [Czech] &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;2,3-Dichlor-1,4-naphthochinon
      &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;2,3-Dichlor-1,4-naphthochinon
      [German] &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;2,3-Dichloro-1,
      4-naphthalenedione &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;2,3-Dichloro-1,4-naphthalenedione
      &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;2,3-Dichloro-1,4-naphthaquinone
      &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;2,3-Dichloro-1,4-naphthoquinone
      &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;2,3-Dichloronaphthoquinone &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;2,3-Dichloronaphthoquinone-1,4
      &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Algistat &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;CDS1_000275 &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;CNQ &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Compound 604 &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Dichlone &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Dichlone [BSI:ISO] &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Dichloronaphthoquinone &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Diclone &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;ENT 3,776 &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Latka 604 [Czech] &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Maybridge1_002563 &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Phygon &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Phygon paste &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Phygon seed protectant &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Phygon XL &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Quintar &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Quintar 540F &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Sanquinon &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;b&gt;&lt;st1:country-region w:st=&quot;on&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;U.s.&lt;/span&gt;&lt;/st1:place&gt;&lt;/st1:country-region&gt;&lt;span lang=&quot;EN&quot;&gt; rubber 604 &lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/b&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;Uniroyal &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;US Rubber 604 &lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: black; mso-list: l0 level2 lfo1; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto; tab-stops: list 72.0pt;&quot;&gt;&lt;span lang=&quot;EN&quot;&gt;&lt;b&gt;USR 604&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;/ol&gt;
&lt;b&gt;
&lt;/b&gt;&lt;br /&gt;
&lt;ol start=&quot;1&quot; style=&quot;margin-top: 0cm;&quot; type=&quot;1&quot;&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;Chemical Formula&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;: C&lt;sub&gt;10&lt;/sub&gt;H&lt;sub&gt;4&lt;/sub&gt;Cl&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;Exact Mass&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;: 225.95883&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;Molecular Weight&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;: 227.04356&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;m/z&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;: 225.96 (100.0%), 227.96 (64.3%), 226.96 (10.9%),
     229.95 (10.2%), 228.96 (7.0%), 230.96 (1.1%) &lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;Elemental Analysis&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;: C, 52.90; H, 1.78; Cl, 31.23;
     O, 14.09&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;Solubility&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;: Acetone, benzene, ether, xylene, &lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;Insoluble&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;: water&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;Appearance: &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;Yellow needle crystal&lt;b&gt;&amp;nbsp; &lt;/b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;Melting Point :&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt; 193&lt;sup&gt;o&lt;/sup&gt;C;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;b&gt;Boiling Point:&lt;/b&gt;&amp;nbsp; 275&lt;sup&gt; o&lt;/sup&gt;C&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;Toxicity&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;: Oral(Rat) : LD50&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-family: &#39;MS Mincho&#39;; line-height: 150%;&quot;&gt;＝&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;1.3g/kg; Carp : LD50&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-family: &#39;MS Mincho&#39;; line-height: 150%;&quot;&gt;＝&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt; 0.07ppm; Red killifish : LD50&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-family: &#39;MS Mincho&#39;; line-height: 150%;&quot;&gt;＝&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt; 0.10ppm&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;Redox Potential&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt; : 498mV&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;Aplication&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;: It is used as algicide and fungicide&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;Uses &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;: agricultural intermediate, catalyst and organic
     synthesis reagent&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;IR (KBr)&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;: 475, 636, 707, 793, 821, 881, 1134, 1274, 1320,
     1388, 1453, 1557, 1585, 1678 (&amp;gt;C=O), 1883, 1985, 2013, 2366 30440,
     3097.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;b&gt;&lt;sup&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;1&lt;/span&gt;&lt;/sup&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;HNMR&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;( 300 MHz, CDCl&lt;sub&gt;3&lt;/sub&gt;): 7.82 (dd, 2H, J=2.4
     &amp;amp; 3.3, C&lt;sub&gt;5&lt;/sub&gt; &amp;amp;C&lt;sub&gt;8&lt;/sub&gt;), 8.19 (dd, 2H, J=2.4 &amp;amp;
     3.3, C&lt;sub&gt;6&lt;/sub&gt; &amp;amp;C&lt;sub&gt;7&lt;/sub&gt;)&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;a href=&quot;http://hardeshkmaurya.blogspot.com/2010/01/23-disubstituted-14-naphthoquinones-12h.html&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;Table 1: Antiproliferative activity &lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;against cervical cancer (HeLa) cells&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;. &lt;/span&gt;&lt;/b&gt;&lt;/a&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;/ol&gt;
&lt;div align=&quot;center&quot;&gt;
&lt;table border=&quot;0&quot; cellpadding=&quot;0&quot; cellspacing=&quot;0&quot; class=&quot;MsoNormalTable&quot; style=&quot;border-collapse: collapse; margin-left: 5.4pt; mso-padding-alt: 0cm 5.4pt 0cm 5.4pt; mso-yfti-tbllook: 480;&quot;&gt;
 &lt;tbody&gt;
&lt;tr&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border-left: none; border-right: none; border-top: solid windowtext 1.0pt; mso-border-bottom-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; padding: 0cm 5.4pt 0cm 5.4pt; width: 57.4pt;&quot; valign=&quot;top&quot; width=&quot;77&quot;&gt;&lt;div align=&quot;right&quot; class=&quot;MsoNormal&quot; style=&quot;text-align: right;&quot;&gt;
&lt;b&gt;&lt;span lang=&quot;EN-US&quot;&gt;Conc.(µM)&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/b&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border-left: none; border-right: none; border-top: solid windowtext 1.0pt; mso-border-bottom-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; padding: 0cm 5.4pt 0cm 5.4pt; width: 76.85pt;&quot; valign=&quot;top&quot; width=&quot;102&quot;&gt;&lt;div align=&quot;right&quot; class=&quot;MsoNormal&quot; style=&quot;text-align: right;&quot;&gt;
&lt;b&gt;&lt;span lang=&quot;EN-US&quot;&gt;Inhibition (%)&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/b&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border-left: none; border-right: none; border-top: solid windowtext 1.0pt; mso-border-bottom-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; padding: 0cm 5.4pt 0cm 5.4pt; width: 55.05pt;&quot; valign=&quot;top&quot; width=&quot;73&quot;&gt;&lt;div align=&quot;right&quot; class=&quot;MsoNormal&quot; style=&quot;text-align: right;&quot;&gt;
&lt;b&gt;&lt;span lang=&quot;EN-US&quot;&gt;SD (±)&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/b&gt;&lt;/div&gt;
&lt;/td&gt;
 &lt;/tr&gt;
&lt;tr&gt;
  &lt;td style=&quot;padding: 0cm 5.4pt 0cm 5.4pt; width: 57.4pt;&quot; valign=&quot;top&quot; width=&quot;77&quot;&gt;&lt;div align=&quot;right&quot; class=&quot;MsoNormal&quot; style=&quot;text-align: right;&quot;&gt;
&lt;span lang=&quot;EN-US&quot;&gt;1&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;padding: 0cm 5.4pt 0cm 5.4pt; width: 76.85pt;&quot; valign=&quot;top&quot; width=&quot;102&quot;&gt;&lt;div align=&quot;right&quot; class=&quot;MsoNormal&quot; style=&quot;text-align: right;&quot;&gt;
&lt;span lang=&quot;EN-US&quot;&gt;28&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;padding: 0cm 5.4pt 0cm 5.4pt; width: 55.05pt;&quot; valign=&quot;top&quot; width=&quot;73&quot;&gt;&lt;div align=&quot;right&quot; class=&quot;MsoNormal&quot; style=&quot;text-align: right;&quot;&gt;
&lt;span lang=&quot;EN-US&quot;&gt;4.2&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;/td&gt;
 &lt;/tr&gt;
&lt;tr&gt;
  &lt;td style=&quot;padding: 0cm 5.4pt 0cm 5.4pt; width: 57.4pt;&quot; valign=&quot;top&quot; width=&quot;77&quot;&gt;&lt;div align=&quot;right&quot; class=&quot;MsoNormal&quot; style=&quot;text-align: right;&quot;&gt;
&lt;span lang=&quot;EN-US&quot;&gt;5&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;padding: 0cm 5.4pt 0cm 5.4pt; width: 76.85pt;&quot; valign=&quot;top&quot; width=&quot;102&quot;&gt;&lt;div align=&quot;right&quot; class=&quot;MsoNormal&quot; style=&quot;text-align: right;&quot;&gt;
&lt;span lang=&quot;EN-US&quot;&gt;43&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;padding: 0cm 5.4pt 0cm 5.4pt; width: 55.05pt;&quot; valign=&quot;top&quot; width=&quot;73&quot;&gt;&lt;div align=&quot;right&quot; class=&quot;MsoNormal&quot; style=&quot;text-align: right;&quot;&gt;
&lt;span lang=&quot;EN-US&quot;&gt;3.6&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;/td&gt;
 &lt;/tr&gt;
&lt;tr&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border: none; mso-border-bottom-alt: solid windowtext .5pt; padding: 0cm 5.4pt 0cm 5.4pt; width: 57.4pt;&quot; valign=&quot;top&quot; width=&quot;77&quot;&gt;&lt;div align=&quot;right&quot; class=&quot;MsoNormal&quot; style=&quot;text-align: right;&quot;&gt;
&lt;span lang=&quot;EN-US&quot;&gt;20&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border: none; mso-border-bottom-alt: solid windowtext .5pt; padding: 0cm 5.4pt 0cm 5.4pt; width: 76.85pt;&quot; valign=&quot;top&quot; width=&quot;102&quot;&gt;&lt;div align=&quot;right&quot; class=&quot;MsoNormal&quot; style=&quot;text-align: right;&quot;&gt;
&lt;span lang=&quot;EN-US&quot;&gt;49&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border: none; mso-border-bottom-alt: solid windowtext .5pt; padding: 0cm 5.4pt 0cm 5.4pt; width: 55.05pt;&quot; valign=&quot;top&quot; width=&quot;73&quot;&gt;&lt;div align=&quot;right&quot; class=&quot;MsoNormal&quot; style=&quot;text-align: right;&quot;&gt;
&lt;span lang=&quot;EN-US&quot;&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp; 4.8&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;/td&gt;
 &lt;/tr&gt;
&lt;/tbody&gt;&lt;/table&gt;
&lt;/div&gt;
&lt;ol start=&quot;17&quot; style=&quot;margin-top: 0cm;&quot; type=&quot;1&quot;&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l0 level1 lfo1; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;line-height: 150%;&quot;&gt;&amp;nbsp;&lt;b&gt; &lt;/b&gt;&lt;b&gt;&lt;a href=&quot;http://hardeshkmaurya.blogspot.com/2010/01/23-disubstituted-14-naphthoquinones-12h.html&quot;&gt;Table 2:      In vitro antifungal      activity (MIC: μg/mL). &lt;/a&gt;&lt;/b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;/ol&gt;
&lt;div align=&quot;center&quot;&gt;
&lt;table border=&quot;1&quot; cellpadding=&quot;0&quot; cellspacing=&quot;0&quot; class=&quot;MsoNormalTable&quot; style=&quot;border-collapse: collapse; border: none; mso-border-alt: solid windowtext .5pt; mso-border-insideh: .5pt solid windowtext; mso-border-insidev: .5pt solid windowtext; mso-padding-alt: 0cm 0cm 0cm 0cm; width: 86.76%;&quot;&gt;
 &lt;tbody&gt;
&lt;tr style=&quot;height: 12.55pt; mso-yfti-firstrow: yes; mso-yfti-irow: 0;&quot;&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border-left: none; border-right: none; border-top: solid windowtext 1.0pt; height: 12.55pt; mso-border-bottom-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; padding: 0cm 0cm 0cm 0cm; width: 14.64%;&quot; width=&quot;14%&quot;&gt;&lt;div align=&quot;center&quot; class=&quot;MsoNormal&quot; style=&quot;mso-layout-grid-align: none; mso-pagination: none; text-align: center; text-autospace: none;&quot;&gt;
&lt;b&gt;&lt;i&gt;&lt;span lang=&quot;EN-US&quot;&gt;C. albicans&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/i&gt;&lt;/b&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border-left: none; border-right: none; border-top: solid windowtext 1.0pt; height: 12.55pt; mso-border-bottom-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; padding: 0cm 0cm 0cm 0cm; width: 18.46%;&quot; width=&quot;18%&quot;&gt;&lt;div align=&quot;center&quot; class=&quot;MsoNormal&quot; style=&quot;mso-layout-grid-align: none; mso-pagination: none; text-align: center; text-autospace: none;&quot;&gt;
&lt;b&gt;&lt;i&gt;&lt;span lang=&quot;EN-US&quot;&gt;C. neoformans&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/i&gt;&lt;/b&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border-left: none; border-right: none; border-top: solid windowtext 1.0pt; height: 12.55pt; mso-border-bottom-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; padding: 0cm 0cm 0cm 0cm; width: 16.52%;&quot; width=&quot;16%&quot;&gt;&lt;div align=&quot;center&quot; class=&quot;MsoNormal&quot; style=&quot;mso-layout-grid-align: none; mso-pagination: none; text-align: center; text-autospace: none;&quot;&gt;
&lt;b&gt;&lt;i&gt;&lt;span lang=&quot;EN-US&quot;&gt;S. schenckii&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/i&gt;&lt;/b&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border-left: none; border-right: none; border-top: solid windowtext 1.0pt; height: 12.55pt; mso-border-bottom-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; padding: 0cm 0cm 0cm 0cm; width: 19.3%;&quot; width=&quot;19%&quot;&gt;&lt;div align=&quot;center&quot; class=&quot;MsoNormal&quot; style=&quot;mso-layout-grid-align: none; mso-pagination: none; text-align: center; text-autospace: none;&quot;&gt;
&lt;b&gt;&lt;i&gt;&lt;span lang=&quot;EN-US&quot;&gt;T. mentagraphytes&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/i&gt;&lt;/b&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border-left: none; border-right: none; border-top: solid windowtext 1.0pt; height: 12.55pt; mso-border-bottom-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; padding: 0cm 0cm 0cm 0cm; width: 14.58%;&quot; width=&quot;14%&quot;&gt;&lt;div align=&quot;center&quot; class=&quot;MsoNormal&quot; style=&quot;mso-layout-grid-align: none; mso-pagination: none; text-align: center; text-autospace: none;&quot;&gt;
&lt;b&gt;&lt;i&gt;&lt;span lang=&quot;EN-US&quot;&gt;A. fumigatus&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/i&gt;&lt;/b&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border-left: none; border-right: none; border-top: solid windowtext 1.0pt; height: 12.55pt; mso-border-bottom-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; padding: 0cm 0cm 0cm 0cm; width: 16.48%;&quot; width=&quot;16%&quot;&gt;&lt;div align=&quot;center&quot; class=&quot;MsoNormal&quot; style=&quot;mso-layout-grid-align: none; mso-pagination: none; text-align: center; text-autospace: none;&quot;&gt;
&lt;b&gt;&lt;span lang=&quot;EN-US&quot;&gt;C.&lt;i&gt; parapsilosis&lt;o:p&gt;&lt;/o:p&gt;&lt;/i&gt;&lt;/span&gt;&lt;/b&gt;&lt;/div&gt;
&lt;/td&gt;
 &lt;/tr&gt;
&lt;tr style=&quot;height: 17.05pt; mso-yfti-irow: 1; mso-yfti-lastrow: yes;&quot;&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border: none; height: 17.05pt; mso-border-bottom-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; padding: 0cm 0cm 0cm 0cm; width: 14.64%;&quot; width=&quot;14%&quot;&gt;&lt;div align=&quot;center&quot; class=&quot;MsoNormal&quot; style=&quot;mso-layout-grid-align: none; mso-pagination: none; text-align: center; text-autospace: none;&quot;&gt;
&lt;span lang=&quot;EN-US&quot;&gt;0.78&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border: none; height: 17.05pt; mso-border-bottom-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; padding: 0cm 0cm 0cm 0cm; width: 18.46%;&quot; width=&quot;18%&quot;&gt;&lt;div align=&quot;center&quot; class=&quot;MsoNormal&quot; style=&quot;mso-layout-grid-align: none; mso-pagination: none; text-align: center; text-autospace: none;&quot;&gt;
&lt;span lang=&quot;EN-US&quot;&gt;3.12&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border: none; height: 17.05pt; mso-border-bottom-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; padding: 0cm 0cm 0cm 0cm; width: 16.52%;&quot; width=&quot;16%&quot;&gt;&lt;div align=&quot;center&quot; class=&quot;MsoNormal&quot; style=&quot;mso-layout-grid-align: none; mso-pagination: none; text-align: center; text-autospace: none;&quot;&gt;
&lt;span lang=&quot;EN-US&quot;&gt;0.78&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border: none; height: 17.05pt; mso-border-bottom-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; padding: 0cm 0cm 0cm 0cm; width: 19.3%;&quot; width=&quot;19%&quot;&gt;&lt;div align=&quot;center&quot; class=&quot;MsoNormal&quot; style=&quot;mso-layout-grid-align: none; mso-pagination: none; text-align: center; text-autospace: none;&quot;&gt;
&lt;span lang=&quot;EN-US&quot;&gt;1.56&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border: none; height: 17.05pt; mso-border-bottom-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; padding: 0cm 0cm 0cm 0cm; width: 14.58%;&quot; width=&quot;14%&quot;&gt;&lt;div align=&quot;center&quot; class=&quot;MsoNormal&quot; style=&quot;mso-layout-grid-align: none; mso-pagination: none; text-align: center; text-autospace: none;&quot;&gt;
&lt;span lang=&quot;EN-US&quot;&gt;1.56&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;/td&gt;
  &lt;td style=&quot;border-bottom: solid windowtext 1.0pt; border: none; height: 17.05pt; mso-border-bottom-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; mso-border-top-alt: solid windowtext .5pt; padding: 0cm 0cm 0cm 0cm; width: 16.48%;&quot; width=&quot;16%&quot;&gt;&lt;div align=&quot;center&quot; class=&quot;MsoNormal&quot; style=&quot;mso-layout-grid-align: none; mso-pagination: none; text-align: center; text-autospace: none;&quot;&gt;
&lt;span lang=&quot;EN-US&quot;&gt;1.56&lt;/span&gt;&lt;/div&gt;
&lt;/td&gt;&lt;/tr&gt;
&lt;/tbody&gt;&lt;/table&gt;
&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot;&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;
&lt;b&gt;&lt;span lang=&quot;EN-US&quot;&gt;&lt;br /&gt;&lt;/span&gt;&lt;/b&gt;&lt;br /&gt;
&lt;b&gt;&lt;span lang=&quot;EN-US&quot;&gt;18 References for
the synthesis of 2,3-dichloro-1,4-naphthoquinone and analogs from 1960-2007&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/b&gt;&lt;/div&gt;
&lt;div align=&quot;center&quot; class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; text-align: center;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 8pt; line-height: 150%;&quot;&gt;(&lt;span style=&quot;color: red;&quot;&gt;Red
reference are showing synthesis and reaction of 2,3-dichlonaphthoquinone&lt;/span&gt;
and &lt;span style=&quot;color: blue;&quot;&gt;Blue reference are showing reaction of
2,3-dichlonaphthoquinone&lt;/span&gt;) &lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;1)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;2,3-Dichloro-1,4-naphthoquinone&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Sjostrand, Bengt Tore
Lennart&lt;span style=&quot;color: red;&quot;&gt;&amp;nbsp; U.S.
2955117, 04 Oct 1960&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;2)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reactions of quinones with aromatic ethers.&amp;nbsp; V.&amp;nbsp;
Triphenylene-1,4-quinones from 2,3-diaryl-1,4-benzoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Buchan, Robert; Musgrave, Oliver C.&lt;span style=&quot;color: red;&quot;&gt;Journal of the Chemical Society, Perkin Transactions 1:&amp;nbsp; Organic and Bio-Organic Chemistry
(1972-1999),&amp;nbsp; (6), 568-72; 1975&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;3)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of some derivatives of 5-amino-1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Slesarchuk, L. P.; Kolesnikov, V. T.;
Boldyrev, B. G.&lt;span style=&quot;color: red;&quot;&gt;Vestnik L&#39;vovskogo Politekhnicheskogo
Instituta, 96, 49-53; 1975&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;4)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naphthoquinone coloring matters.&amp;nbsp; Part 2.&amp;nbsp;
1,4-Naphthoquinones with electron-donating groups in the benzenoid ring.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Chu, Kwong-Yung; &lt;st1:city w:st=&quot;on&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;Griffiths&lt;/st1:place&gt;&lt;/st1:city&gt;, John.&lt;span style=&quot;color: red;&quot;&gt;Journal
of Chemical Research, Synopses, (5), 180-1; 1978&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;5)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;A convenient synthesis of some highly functionalized
chromones and indenones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Roberge, Guy; Brassard, Paul. &lt;span style=&quot;color: red;&quot;&gt;Synthetic Communications, 9(2), 129-39; 1979&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;6)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reaction of &lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; -hydroxyanthraquinones
with thionyl chloride.&amp;nbsp; Preparation of
1,10-anthraquinone derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Gorelik, M. V.; Titova, S. P.; Trdatyan, V.
A.&amp;nbsp;&amp;nbsp;&amp;nbsp; Nauchno-Issled. Inst. Org.
Poluprod. Krasitelei&lt;span style=&quot;color: red;&quot;&gt; Zhurnal Organicheskoi Khimii, 15(1),
157-66; 1979&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;7)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthetic studies of naphthoquinone derivatives.&amp;nbsp; 3.&amp;nbsp;
Reactions of 5-substituted 2,3-dichloro- and
2,3,6,8-tetrachloro-1,4-naphthoquinones with anilines.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;&lt;st1:place w:st=&quot;on&quot;&gt;Kasai&lt;/st1:place&gt;,
Toshiyasu; Nakamori, Tateo; Sekiguchi, Kyoichi. &lt;st1:place w:st=&quot;on&quot;&gt;&lt;span style=&quot;color: red;&quot;&gt;Nippon&lt;/span&gt;&lt;/st1:place&gt;&lt;span style=&quot;color: red;&quot;&gt; Kagaku
Kaishi,&amp;nbsp; (12), 1862-9; 1980&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;8)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Studies of the synthesis of naphthoquinone derivatives.&amp;nbsp; 4.&amp;nbsp;
Reactions of aniline with 2,3-dichloro-1,4-naphthoquinones having
additional chloro substituents on the benzenoid ring.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;&lt;st1:place w:st=&quot;on&quot;&gt;Kasai&lt;/st1:place&gt;,
Toshiyasu; Nakamori, Tateo; Sawayama, Akio.&lt;span style=&quot;color: red;&quot;&gt;Nippon
Kagaku Kaishi,&amp;nbsp; (3), 416-23; 1981&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;9)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of naphthoquinone derivatives.&amp;nbsp; V.&amp;nbsp;
Synthesis of 2,3-disubstituted 5,8-diamino-1,4-naphthoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;&lt;st1:place w:st=&quot;on&quot;&gt;Kasai&lt;/st1:place&gt;,
Toshiyasu; Nakamori, Tateo; Furugaki, Koichi.&lt;span style=&quot;color: red;&quot;&gt;Nippon
Kagaku Kaishi,&amp;nbsp; (4), 536-43; 1981&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;10)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis, reactions and spectra of some fused polycyclic
aromatic chlorocarbons, and related compounds.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
&lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Ballester, M.; Castaner, J.; Riera, J.;
Pares, J. &lt;span style=&quot;color: red;&quot;&gt;Anales de Quimica, Serie C:&amp;nbsp; Quimica Organica y Bioquimica, 76(2), 157-70;
1980&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;11)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;A convenient synthesis of
2,3-dichloro-1,4-naphthoquinone-1-14C using a novel chlorination procedure.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Ehler, Kenneth W.; Pardini, Ronald S.&lt;span style=&quot;color: red;&quot;&gt;Organic Preparations and Procedures International, 15(3),
157-60; 1983&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;12)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naphthoquinone antipsoriatic agents.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Jones, Gordon H.; Young, John M. &lt;span style=&quot;color: red;&quot;&gt;U.S., 4442127, 10 Apr 1984&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;13)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Study of 1,4-naphthoquinone.&amp;nbsp;
VIII.&amp;nbsp; Nucleophilic substitution
in a series of 2,3-dichloro-5-hydroxy-1,4-naphthoquinone and its derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Belitskaya, L. D.; Kolesnikov, V. T.&lt;span style=&quot;color: red;&quot;&gt;Zhurnal Organicheskoi Khimii, 20(9), 1920-5; 1984&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;14)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Site-selective Diels-Alder reactions of
1,4,5,8-naphthodiquinones with anthracenes and successively with
cyclopentadiene:&amp;nbsp; electronic effects vs.
steric effects.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Hayakawa, Kenji; Aso, Mariko; Kanematsu, Ken.
&lt;span style=&quot;color: red;&quot;&gt;Journal of Organic Chemistry, 50(12), 2036-40; 1985&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;15)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Acyloxynaphthalene antipsoriatic agents.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Jones, Gordon H.; Venuti, Michael C.; Young,
John M. &lt;span style=&quot;color: red;&quot;&gt;Eur. Pat. Appl., 146145, 26 Jun 1985&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;16)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Sulfonation and sulfochlorination of
2,3-dichloro-1,4-naphthoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Shishkina, R. P.; Mamatyuk, V. I.; Fokin, E.
P. &lt;span style=&quot;color: red;&quot;&gt;Izvestiya Akademii Nauk SSSR, Seriya
Khimicheskaya,&amp;nbsp; (4), 855-7; 1985&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;17)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Dimeric naphthoquinones.&amp;nbsp;
XVI.&amp;nbsp; Synthesis of maritinone and
other 8,8&#39;-bijuglones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Laatsch, Hartmut. &lt;span style=&quot;color: red;&quot;&gt;Liebigs
Annalen der Chemie,&amp;nbsp; (12), 2420-42; 1985&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;18)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;2,3-Dichloro-1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
&lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Suzuki, Hisashi; Yabe, Hirota.&amp;nbsp; &lt;span style=&quot;color: red;&quot;&gt;Jpn. Kokai Tokkyo
Koho, 61018742, 27 Jan 1986, Showa&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;19)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Topical nonsteroidal antipsoriatic agents.&amp;nbsp; 1.&amp;nbsp;
1,2,3,4-Tetraoxygenated naphthalene derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Jones, Gordon H.; Venuti, Michael C.; Young,
John M.; Murthy, D. V. Krishna; Loe, Brad E.; Simpson, Richard A.; Berks,
Andrew H.; Spires, Doreen A.; Maloney, Patrick J.; et al. &lt;span style=&quot;color: red;&quot;&gt;Journal of Medicinal Chemistry, 29(8), 1504-11; 1986&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;20)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;1,4-Anthraquinonoid dienophiles applicable to synthesis of
linear tetracycles.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Cameron, Donald W.; Conn, Costa; Crossley,
Maxwell J.; Feutrill, Geoffrey I.; Fisher, Mark W.; Griffiths, Peter G.;
Merrett, Bryan K.; Pavlatos, Dennis.&lt;span style=&quot;color: red;&quot;&gt;Tetrahedron
Letters, 27(21), 2417-20; 1986&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;21)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthetic studies of the rubradirins.&amp;nbsp; A strategy for the incorporation of the ansa
bridge.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kozikowski, Alan P.; Xia, Yan.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;span style=&quot;color: red;&quot;&gt;Journal of Organic
Chemistry, 52(7), 1375-8; 1987&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;22)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naphthalene antipsoriatic and antiinflammatory agents and
lipoxygenase inhibitors and a process for making them.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;&lt;st1:place w:st=&quot;on&quot;&gt;Krishna&lt;/st1:place&gt; Murthy, Dodballapur Venkataramiah; Young, John
M.; Venuti, Michael C.&amp;nbsp; &lt;span style=&quot;color: red;&quot;&gt;Eur. Pat. Appl., 215622, 25 Mar 1987&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;23)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Preparation of 5-hydroxynaphtho[2,3-d]thiazole-4,9-dione as
medical bactericide.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Nishino, Isao; Kimura, Harutaka.&amp;nbsp; &lt;span style=&quot;color: red;&quot;&gt;Jpn. Kokai Tokkyo
Koho, 62234076, 14 Oct 1987, Showa&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;24)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Preparation of 5-hydroxynaphtho[2,3-d]thiazole-4,9-dione as a
veterinary bactericide.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Nishino, Isao; Kimura, Harutaka; Araki,
Seiichi. &lt;span style=&quot;color: red;&quot;&gt;Jpn. Kokai Tokkyo Koho, 62234019, 14 Oct 1987,
Showa&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;25)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and cytotoxic activity of
aziridinyl-1,4-naphthoquinones and -naphthazarins.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
&lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Horowska, Barbar; Mazerska, Zofia;
Ledochowski, Andrzej; Cristalli, Gloria; Franchetti, Palmarisa; Martelli,
Sante. &lt;span style=&quot;color: red;&quot;&gt;European Journal of Medicinal Chemistry, 23(1),
91-6; 1988&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;26)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthetic studies on nogalamycin congeners.&amp;nbsp; II.&amp;nbsp;
Chiral synthesis of the CDEF-ring system of nogalamycin.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;&lt;st1:city w:st=&quot;on&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;Kawasaki&lt;/st1:place&gt;&lt;/st1:city&gt;,
Motoji; Matsuda, Fuyuhiko; Terashima, Shiro. &lt;span style=&quot;color: red;&quot;&gt;Tetrahedron,
44(18), 5713-25; 1988&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;27)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Fries rearrangement and Dakin reaction in the
benzo-2,1,3-thiadiazole series.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Belen&#39;kaya, I. A.; Krokhina, G. P.; Sirik, S.
A.; Andronati, S. A. &lt;span style=&quot;color: red;&quot;&gt;Khimiya Geterotsiklicheskikh
Soedinenii,&amp;nbsp; (12), 1683-7; 1987&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;28)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naphthazarin derivatives as antitumor agents.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Masuda, Kazuaki.&amp;nbsp; &lt;span style=&quot;color: red;&quot;&gt;Jpn. Kokai Tokkyo
Koho, 62289543, 16 Dec 1987, Showa&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;29)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Electronic structure and near-infrared spectra of diquinone
anion radicals.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Almlof, Jan E.; Feyereisen, Martin W.;
Jozefiak, Thomas H.; Miller, Larry L.&lt;span style=&quot;color: red;&quot;&gt;Journal of the
American Chemical Society, 112(3), 1206-14; 1990&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;30)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Dichloroquinones as dienophiles:&amp;nbsp; synthesis of alizarin derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Cameron, Donald W.; Feutrill, Geoffrey I.;
Keep, Philip L. C.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;span style=&quot;color: red;&quot;&gt;Tetrahedron Letters, 30(38), 5173-6; 1989&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;31)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chlorination of 1,4-naphthoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kitahara, Tadao; Kitahara, Satoru; Minemura,
Muneharu; Akyama, Ukichi.&lt;span style=&quot;color: red;&quot;&gt;Jpn. Kokai Tokkyo Koho,
03246250, 01 Nov 1991, Heisei&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;32)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;The Pursuit of Perchlorotriphenylene.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Shibata, Kazusato; Kulkarni, Abhijit A.; Ho,
Douglas M.; Pascal, Robert A., Jr. &lt;span style=&quot;color: red;&quot;&gt;Journal of Organic
Chemistry, 60(2), 428-34; 1995&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;33)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Use of Thiazyl Chlorides, Alkyl Carbamates, and Thionyl
Chloride To Fuse 1,2,5-Thiadiazoles to Quinones and To Oxidize, Chlorinate, and
Aminate Them.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Shi, Shuhao; Katz, Thomas J.; Yang, Bingwei
V.; Liu, Longbin. &lt;span style=&quot;color: red;&quot;&gt;Journal of Organic Chemistry, 60(5),
1285-97; 1995&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;34)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and Characterization of Novel Donor-Acceptor
Naphthoquinone Derivatives with Photoinduced Charge-Transfer Properties. A
Joint Experimental and Theoretical Study.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
&lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Illescas, Beatriz; Martin, Nazario; Segura,
Jose L.; Seoane, C.; Orti, Enrique; Viruela, Pedro M.; Viruela, Rafael.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;span style=&quot;color: red;&quot;&gt;Journal of Organic
Chemistry, 60(17), 5643-50; 1995&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;35)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chemistry of naphthazarin derivatives. Reaction of
unsubstituted and substituted 2,5,8-trihydroxy-1,4-naphthoquinones and
derivatives of 2,5,8-trihydroxy-1,4-naphthoquinone 1-imines with citral.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Chizhova, A. Ya.; Anufriev, V. F.; Novikov,
V. L. &lt;span style=&quot;color: red;&quot;&gt;Zhurnal Organicheskoi Khimii, 31(2), 237-43; 1995&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;36)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of acetyl- and methoxycarbonylnaphthazarins.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Farina, F.; Valderrama, J. A.; Gonzalez, L. &lt;span style=&quot;color: red;&quot;&gt;Anales de Quimica, 91(5-6), 440-448; 1995&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;37)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.informaworld.com/smpp/content~db=ai~content=a747161737?words=&amp;amp;hash=3799665758&quot; title=&quot;Click to view this record&quot;&gt;A Benzylation Study of
2,3-Dichloronaphthazarin&lt;/a&gt;&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;. Cheng, C. C.;&amp;nbsp; Chang, He Xi;&amp;nbsp; Morton, Martha;
Velde,&lt;/span&gt;&lt;i&gt;&lt;span lang=&quot;EN-US&quot;&gt; &lt;/span&gt;&lt;/i&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;David Vander &lt;span style=&quot;color: red;&quot;&gt;&amp;nbsp;Synthetic
Communications, 26(10), 1985-93; 1996&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;38)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;The synthesis of a symmetrically substituted-&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-family: Symbol; font-size: 10pt; line-height: 150%;&quot;&gt;a&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;
-octa(isopentoxy)anthralocyanine&lt;span style=&quot;color: #9c0000;&quot;&gt;&amp;nbsp; &lt;/span&gt;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bedworth,
Peter V.; Perry Joseph W. ; Marder, Seth R.&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;Chemical
Communications (&lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:city w:st=&quot;on&quot;&gt;Cambridge&lt;/st1:city&gt;&lt;/st1:place&gt;),&amp;nbsp; (15), 1353-1354; 1997&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;39)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of Hallachrome&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot;&gt;. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Cameron,
Donald W.; Coller, D. Ross; McDonald,&lt;/span&gt;&lt;i&gt;&lt;span lang=&quot;EN-US&quot;&gt; &lt;/span&gt;&lt;/i&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&amp;nbsp;&lt;/span&gt;&lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:city w:st=&quot;on&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Clinton&lt;/span&gt;&lt;/st1:city&gt;&lt;/st1:place&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; A. &amp;nbsp;&lt;span style=&quot;color: red;&quot;&gt;Australian Journal of
Chemistry, 52(9), 833-836; 1999&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;40)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of organic third-order nonlinear optical materials
of dioxonaphthothiazole and dibenzothianthrene compounds.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;Gao, Jian-rong; Shen, Wei-guang; Cheng,
Lu-bai; Chen, Xing. &lt;st1:state w:st=&quot;on&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;&lt;span style=&quot;color: red;&quot;&gt;Zhejiang&lt;/span&gt;&lt;/st1:place&gt;&lt;/st1:state&gt;&lt;span style=&quot;color: red;&quot;&gt; Gongye Daxue Xuebao, 28(1), 14-17; 2000&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;41)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Regiocontrolled synthesis of the trimeric quinone framework
of conocurvone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Emadi, Ashkan; Harwood, John S.; Kohanim,
Sahar; Stagliano, Kenneth W. &lt;span style=&quot;color: red;&quot;&gt;Organic Letters, 4(4),
521-524; 2002&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;42)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Sonochemical chloro-oxidation of phenols using HCl-H2O2.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Bhatkhande, B. S.; Adhikari, M. V.; Samant,
S. D.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;span style=&quot;color: red;&quot;&gt;Ultrasonics
Sonochemistry, 9(1), 31-35; 2002&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;43)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naturalization and modification of natural colors of flowers.
I. Naphthofuroquinolinedione dyes.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Boscornea, Cristian; Pasolea, &lt;st1:place w:st=&quot;on&quot;&gt;Florin&lt;/st1:place&gt;; Tarabasanu Mihaila, Corneliu; Boscornea, Corina. &lt;span style=&quot;color: red;&quot;&gt;Revista de Chimie (&lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:city w:st=&quot;on&quot;&gt;Bucharest&lt;/st1:city&gt;,
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53(5), 394-403; 2002&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;44)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Pigments of fungi. Part 70. Total synthesis of (R)-semixanthomegnin
and the x-ray crystal structure of (&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;
)-7-chloro-10-methoxy-3-methyl-3,4-dihydro-1H-naphtho[2,3-c]pyran-1,6,9-trione.
&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;Australian Journal of Chemistry, 56(1), 49-57; 2003&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;45)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chemistry of naphthazarin derivatives. 9. Direct observation
of prototropic tautomerism of (poly)hydroxynaphthazarins by IR spectroscopy.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Glazunov, V. P.; Yakubovskaya, A. Ya.;
Pokhilo, N. D.; Bochinskaya, N. V.; Anufriev, V. Ph. &lt;span style=&quot;color: red;&quot;&gt;Russian
Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya
Khimicheskaya), 52(1), 198-207; 2003&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;46)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Process for preparation of
naphthoquinonothiazole derivatives as organic third-order non-linear optical
materials.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Gao, Jianrong; Sheng, Weijian; Xiang, Bin;
Shan, Weiguang; Cheng, Lubai. &lt;span style=&quot;color: red;&quot;&gt;Faming Zhuanli Shenqing
Gongkai Shuomingshu, 1440966, 10 Sep 2003&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;47)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;PCT Int. Appl., 2005095376, 13 Oct 2005&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Preparation of naphthoquinone derivatives as PI3 kinase
inhibitors for treatment of cancer.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
&lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Chang, Junbiao; Xie, Weilin; Wang, Lei. &lt;span style=&quot;color: red;&quot;&gt;Faming Zhuanli Shenqing Gongkai Shuomingshu, 1587255, 02 Mar
2005&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of 1,4,5,8-tetramethoxynaphthalene-2-carboxaldehyde.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Xu, Defeng; Guan, Pengjian; Mao, Zhiqiang;
Wang, Zhenmo; Li, Shaoshun&lt;span style=&quot;color: red;&quot;&gt;&amp;nbsp; Zhongguo Yiyao Gongye Zazhi, 35(10), 583-585;
2004&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
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&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;50)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and antifungal activity of naphthalene-1,4-diones
modified at positions 2, 3, and 5.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Ryu, Chung-Kyu; Chae, Mi Jin. &lt;span style=&quot;color: red;&quot;&gt;Archives of Pharmacal Research, 28(7), 750-755; 2005&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;51)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;New cytotoxic furoquinones obtained from
terpenyl-1,4-naphthoquinones and 1,4-anthracenediones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Miguel del Corral, Jose M.; Castro, M.
Angeles; Oliveira, Alaide B.; Gualberto, Simone A.; Cuevas, Carmen; San
Feliciano, Arturo.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;span style=&quot;color: red;&quot;&gt;Bioorganic &amp;amp; Medicinal Chemistry, 14(21), 7231-7240; 2006&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;52)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Study on synthesis of 2,3-dichloro-1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Cao, Xiao-qun; Liu, Xin; Cheng,
Yue-shan.&amp;nbsp;&amp;nbsp; &lt;span style=&quot;color: red;&quot;&gt;Jingxi
Yu Zhuanyong Huaxuepin, 14(3/4), 16-17; 2006&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;53)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Quinone antitumor compounds, particularly 1,4-anthraquinones
and their derivatives, process for their preparation, and their uses.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Molina Orden, Maria Teresa; Honghao, Sun;
Taliansky Chamudis, Sandra; Carnero Moya, Amancio; Blanco Rodriguez, Fernando;
Moneo Ocana, Maria Victoria. &lt;span style=&quot;color: red;&quot;&gt;PCT Int. Appl.,
2007026041, 08 Mar 2007&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;54)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;Chinese Chemical Letters, 17(7), 871-873; 2006&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 36.0pt; mso-list: l8 level1 lfo2; tab-stops: list 36.0pt; text-indent: -18.0pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;55)&lt;span style=&quot;font-family: &#39;Times New Roman&#39;; font-size: 7pt; font-style: normal; font-variant: normal; font-weight: 400; line-height: normal;&quot;&gt;&amp;nbsp;&amp;nbsp;
&lt;/span&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;Hecheng Huaxue, 15(1), 16-19; 2007&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; margin-left: 18.0pt; tab-stops: 152.05pt;&quot;&gt;
&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp;&amp;nbsp;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;MsoNormal&quot; style=&quot;line-height: 150%;&quot;&gt;
&lt;b&gt;&lt;span lang=&quot;EN-US&quot;&gt;References for
the reaction of 2,3-dichloro-1,4-naphthoquinone and analogs (1954-2007):&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/b&gt;&lt;/div&gt;
&lt;ol start=&quot;1&quot; style=&quot;margin-top: 0cm;&quot; type=&quot;1&quot;&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Preparation of
     some imidazole derivatives of 1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;&lt;st1:city w:st=&quot;on&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;Hoover&lt;/st1:place&gt;&lt;/st1:city&gt;,
     John R. E.; Day, Allan R. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of the American Chemical Society, 76, 4148-52;
     1954&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of
     substituted amino, aminovinyl, and aminobutadienyl-p-quinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Buckley, D.; Henbest, H. B.; Slade, P. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of the
     Chemical Society, 4891-900; 1957&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reactions
     between quinones and unsaturated amines. II. Detection of
     N-alkylvinylamines in equilibrium with ethylideneamines.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Honbest, H. B.; Slade, P. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of the
     Chemical Society, 1555-7; 1960&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Amine
     oxidation. V. Dehydrogenation of diethylamine in the presence of
     2,3-dichloronaphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Henbest, H. B.; Slade, P. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of the
     Chemical Society, 1558-60; 1960&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;2,3-Dichloro-1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Sjostrand, Bengt Tore Lennart.&amp;nbsp; &lt;/span&gt;&lt;st1:country-region w:st=&quot;on&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;U.S.&lt;/span&gt;&lt;/st1:place&gt;&lt;/st1:country-region&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; 2955117, 04 Oct 1960&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reactions of &lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; -dicarbonyl compounds and
     quinones with diazoalkanes. V. Reactions of substituted p-benzo- and
     -naphthoquinones with diazomethane.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Eistert, Bernd; Fink, Herbert; Mueller,
     Anneliese. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chemische Berichte, 95, 2403-15; 1962&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Heterocyclic
     quinones from 2,3-dichloro-1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Sartori, M.
     F.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chem. Rev., 63, 279-96; 1963&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reaction of
     2,3-dichloronaphthoquinone with nucleophiles. II. Reaction with ethyl
     acetoacetate.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Reynolds, G. A.; VanAllan, J. A.; Adel,
     R. E.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Organic Chemistry, 30(11),
     3819-24; 1965&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;2,3,5,6-Tetraamino-1,4-benzoquinone.&amp;nbsp; Preparation, properties, and reactions.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Winkelmann, Erhardt.&amp;nbsp;&amp;nbsp;&amp;nbsp; Farbwerke Hoechst A.-G.,&amp;nbsp; Frankfurt/M., &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron, 25(12), 2427-54;
     1969&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;4,9-Methano[11]annulenone.&amp;nbsp; Ten-&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; -electron analog of tropone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Vogel, Emanuel; Grimme, Walter;
     Reisdorff, J.; Juenemann, W.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of the
     American Chemical Society, 92(21), 6335-7; 1970&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Experiments to
     study meson resonances.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Clark, Alan R.; Conforto, G.; Kenney, V.
     P.; Key, A. W.; Neal, H. A.; Pine, J. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;U. S. At. Energy Comm.,&amp;nbsp; (TID-25473(Vol. 4)), 237-66; 1969&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reactions of
     quinones with aromatic ethers.&amp;nbsp;
     V.&amp;nbsp; Triphenylene-1,4-quinones
     from 2,3-diaryl-1,4-benzoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Buchan, Robert; Musgrave, Oliver C. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of the Chemical
     Society, Perkin Transactions 1:&amp;nbsp;
     Organic and Bio-Organic Chemistry (1972-1999),&amp;nbsp; (6), 568-72; 1975&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Cyclization
     reactions of quinonylmethane dyes and analogous merocyanines.&amp;nbsp; 3.&amp;nbsp;
     Quinoid derivatives of anellated
     tetrahydroisoquinolinoquinoxaline.&amp;nbsp;
     Cyclization following the 1,7-shift of hydrogen.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Schelz, Dieter; Priester, Martin. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Helvetica Chimica
     Acta, 58(8), 2536-45; 1975&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Studies on
     benzimidazole derivatives.&amp;nbsp; XL.&amp;nbsp; Reaction of mercapto derivatives of
     azoles with haloquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Simonov, A. M.; Komissarov, V. N.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Khimiya Geterotsiklicheskikh
     Soedinenii,&amp;nbsp; (6), 783-5; 1976&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of
     some derivatives of 5-amino-1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Slesarchuk, L. P.; Kolesnikov, V. T.;
     Boldyrev, B. G. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Vestnik L&#39;vovskogo Politekhnicheskogo Instituta, 96, 49-53;
     1975&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and
     properties of charge transfer complexes and autocomplexes.&amp;nbsp; XVIII.&amp;nbsp;
     Some water-soluble derivatives of 1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Dregeris, J.; Liepina, &lt;st1:place w:st=&quot;on&quot;&gt;I.&lt;/st1:place&gt;;
     Freimanis, J.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Latvijas PSR Zinatnu
     Akademijas Vestis, Kimijas Serija,&amp;nbsp;
     (4), 460-4; 1977&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reactions of ketene acetals.&amp;nbsp; IX. The synthesis of naphthoquinones
     from benzoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Grandmaison, Jean Louis; Brassard,
     Paul.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;span style=&quot;color: blue;&quot;&gt;Tetrahedron,
     33(16), 2047-53; 1977&lt;/span&gt;&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;A convenient synthesis of naphthazarin and
     naphthopurpurin.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Lewis, John R.; Paul, John.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;span style=&quot;color: blue;&quot;&gt;Anorganische
     Chemie, Organische Chemie&amp;nbsp;
     (1977),&amp;nbsp; 32B(12),&amp;nbsp; 1473-5.&lt;/span&gt;&amp;nbsp; &lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naphthoquinone
     coloring matters.&amp;nbsp; Part 2.&amp;nbsp; 1,4-Naphthoquinones with
     electron-donating groups in the benzenoid ring.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;&lt;st1:place w:st=&quot;on&quot;&gt;Chu&lt;/st1:place&gt;,
     Kwong-Yung; Griffiths, John. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Chemical Research, Synopses,&amp;nbsp; (5), 180-1; 1978&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and
     IR spectra of some new benzo[a] phenazine derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Agarwal, N. L.; Mital, R. L. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Philippine Journal of
     Science, 105(3), 125-32; 1978&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;A convenient
     synthesis of some highly functionalized chromones and indenones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Roberge, Guy; Brassard, Paul. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthetic
     Communications, 9(2), 129-39; 1979&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reaction of &lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; -hydroxyanthraquinones with
     thionyl chloride.&amp;nbsp; Preparation of
     1,10-anthraquinone derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Gorelik, M. V.; Titova, S. P.; Trdatyan,
     V. A.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Zhurnal Organicheskoi Khimii,
     15(1), 157-66; 1979&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;A convenient
     method for the synthesis of naphtho[2,3-b]furan-4,9-diones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kuo, Hsien-Saw; Hotta, Kazuo; Yogo,
     Motoi; Yoshina, Shigetaka. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis,&amp;nbsp; (3),
     188-9; 1979&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naphthoquinone
     coloring matters.&amp;nbsp; Part 4.&amp;nbsp; Amino-substituted
     1,2-dimethylnaphth[2,3-d]imidazole-4,9-diones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Green-Buckley, Graham; Griffiths, John. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of the
     Chemical Society, Perkin Transactions 1:&amp;nbsp;
     Organic and Bio-Organic Chemistry (1972-1999),&amp;nbsp; (3), 702-7; 1979&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naphthoquinone
     coloring matters.&amp;nbsp; Part 3.&amp;nbsp; Synthesis and electronic absorption
     spectra of 1,4-naphthoquinones containing electron donor groups in both
     rings.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;&lt;st1:place w:st=&quot;on&quot;&gt;Chu&lt;/st1:place&gt;,
     Kwong Yung; Griffiths, John. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of the Chemical Society, Perkin
     Transactions 1:&amp;nbsp; Organic and
     Bio-Organic Chemistry (1972-1999),&amp;nbsp;
     (3), 696-701; 1979&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Heterocyclic
     quinonoid chromophoric systems:&amp;nbsp;
     Part II.&amp;nbsp; Reaction of
     2,3-dichloro-1,4-naphthoquinone with
     3-cyano-4-methyl-6-hydroxy-2(1H)-pyridone and its N-substituted derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Ayyangar, N. R.; Kolhe, P. Y.; Tilak, B.
     D. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Indian
     Journal of Chemistry, Section B:&amp;nbsp;
     Organic Chemistry Including Medicinal Chemistry, 17B(2), 100-3;
     1979&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Angular
     heterocycles:&amp;nbsp; synthesis of some
     substituted p-bromoanilino-12H-benzo[a]phenothiazines.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Tiwari, J. P.; Mital, R. L.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Indian Journal of Chemistry,
     Section B:&amp;nbsp; Organic Chemistry
     Including Medicinal Chemistry, 17B(4), 408-9; 1979&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and
     properties of charge transfer complexes and autocomplexes.&amp;nbsp; XXIV.&amp;nbsp;
     Synthesis of molecular autocomplexes of a series of
     1,4-naphthoquinone containing long hydrocarbon chains.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Dregeris, J.; Novicka, D.; Freimanis, J.
     &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Latvijas
     PSR Zinatnu Akademijas Vestis, Kimijas Serija,&amp;nbsp; (6), 692-7; 1979&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Studies on the
     syntheses of condensed indole-4,7-dione derivatives.&amp;nbsp; I.&amp;nbsp;
     Syntheses of benz[f]indole-4,9-diones starting from
     2,3-dichloronaphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Okamoto, Masao; Ohta, Shunsaku; Terada,
     Shinichiro. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Yakugaku Zasshi, 99(12), 1219-24; 1979&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of
     2-chloro-3-anilino-5-hydroxy-1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kolesnikov, V. T. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Visnik L&#39;viv.
     Politekhn. In-tu,&amp;nbsp; (131), 70-2; 1979&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Some
     chloroacetylamino derivatives of 5-nitro- and 5-amino-1,4-naphthoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Slesarchuk, L. P.; Kolesnikov, V.
     T.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Visnik L&#39;viv. Politekhn.
     In-Tu&amp;nbsp; (1979),&amp;nbsp;&amp;nbsp; (131),&amp;nbsp;
     66-9&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Heterocyclic
     quinonoid chromophoric systems.&amp;nbsp;
     Part VI.&amp;nbsp; Reaction of
     2,3-dichloro-1,4-naphthoquinone with homophthalimides and other compounds
     containing a reactive methylene group.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Ayyangar, N. R.; Kolhe, P. Y.; Tilak, B.
     D. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Indian
     Journal of Chemistry, Section B:&amp;nbsp;
     Organic Chemistry Including Medicinal Chemistry, 19B(10), 836-43;
     1980&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthetic
     studies of naphthoquinone derivatives.&amp;nbsp;
     3.&amp;nbsp; Reactions of
     5-substituted 2,3-dichloro- and 2,3,6,8-tetrachloro-1,4-naphthoquinones
     with anilines.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;st1:place w:st=&quot;on&quot;&gt;Kasai&lt;/st1:place&gt;,
     Toshiyasu; Nakamori, Tateo; Sekiguchi, Kyoichi.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;st1:place w:st=&quot;on&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Nippon&lt;/span&gt;&lt;/st1:place&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Kagaku Kaishi,&amp;nbsp; (12), 1862-9; 1980&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reaction of
     2,3-dichloro-5-hydroxy-1,4-naphthoquinone with sodium methylate.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kolesnikov, V. T.; Belitskaya, L. D.;
     Rozhilo, L. G. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Vestnik L&#39;vovskogo Politekhnicheskogo Instituta, 139, 112-14; 1980&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis,
     reactions and spectra of some fused polycyclic aromatic chlorocarbons, and
     related compounds.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Ballester, M.; Castaner, J.; Riera, J.;
     Pares, J. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Anales de Quimica, Serie C:&amp;nbsp;
     Quimica Organica y Bioquimica, 76(2), 157-70; 1980&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Quinone chemistry.&amp;nbsp; Reaction of
     2,3-dichloro-1,4-naphthoquinone with o-aminophenols under various
     conditions.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Agarwal, Nand L.; Schaefer, Wolfram. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Organic
     Chemistry, 45(11), 2155-61; 1980&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Quinone
     chemistry.&amp;nbsp; Reaction of
     2,3-dichloro-1,4-naphthoquinone with arylamines in pyridine.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Agarwal, Nand L.; Schaefer, Wolfram.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Organic
     Chemistry, 45(25), 5139-43; 1980&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Quinone
     chemistry.&amp;nbsp; Reaction of
     2,3-dichloro-1,4-naphthoquinone with 2-aminophenols in pyridine.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Agarwal, Nand L.; Schaefer, Wolfram.b &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Organic
     Chemistry, 45(25), 5144-9; 1980&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Studies of the
     synthesis of naphthoquinone derivatives.&amp;nbsp;
     4.&amp;nbsp; Reactions of aniline with
     2,3-dichloro-1,4-naphthoquinones having additional chloro substituents on
     the benzenoid ring.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;&lt;st1:place w:st=&quot;on&quot;&gt;Kasai&lt;/st1:place&gt;,
     Toshiyasu; Nakamori, Tateo; Sawayama, Akio. &lt;/span&gt;&lt;st1:place w:st=&quot;on&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Nippon&lt;/span&gt;&lt;/st1:place&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Kagaku Kaishi,&amp;nbsp; (3), 416-23; 1981&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of
     naphthoquinone derivatives.&amp;nbsp; V.&amp;nbsp; Synthesis of 2,3-disubstituted
     5,8-diamino-1,4-naphthoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;&lt;st1:place w:st=&quot;on&quot;&gt;Kasai&lt;/st1:place&gt;,
     Toshiyasu; Nakamori, Tateo; Furugaki, Koichi. &lt;/span&gt;&lt;st1:place w:st=&quot;on&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Nippon&lt;/span&gt;&lt;/st1:place&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Kagaku Kaishi,&amp;nbsp; (4), 536-43; 1981&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of
     naphthoquinone derivatives.&amp;nbsp;
     VI.&amp;nbsp; Reactions of
     2,3-dicyano-1,4-naphthoquinone with nucleophiles.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Nakamori, Tateo; Okano, Takashi; &lt;st1:place w:st=&quot;on&quot;&gt;Kasai&lt;/st1:place&gt;, Toshiyasu. &lt;/span&gt;&lt;st1:place w:st=&quot;on&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Nippon&lt;/span&gt;&lt;/st1:place&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Kagaku Kaishi,&amp;nbsp; (8), 1287-94; 1981&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of
     naphthoquinone derivatives.&amp;nbsp; 7.&amp;nbsp; Reactions of
     5-amino-2,3-dicyano-1,4-naphthoquinone with anilines.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Nakamori, Tateo; &lt;st1:city w:st=&quot;on&quot;&gt;Chiba&lt;/st1:city&gt;,
     Tuneo; &lt;st1:place w:st=&quot;on&quot;&gt;Kasai&lt;/st1:place&gt;, Toshiyasu. &lt;/span&gt;&lt;st1:place w:st=&quot;on&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Nippon&lt;/span&gt;&lt;/st1:place&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Kagaku Kaishi,&amp;nbsp; (12), 1916-21; 1981&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reaction of
     chloranil and 2,3-dichloronaphthoquinone with benzylmagnesium chloride.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Denisov, V. Ya.; Pozdnyakov, O. V.&amp;nbsp;&amp;nbsp;&amp;nbsp; Kemer. Gos. Univ.,&amp;nbsp; &lt;st1:city w:st=&quot;on&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;Kemerovo&lt;/st1:place&gt;&lt;/st1:city&gt;,
     &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Izvestiya
     Vysshikh Uchebnykh Zavedenii, Khimiya i Khimicheskaya Tekhnologiya,
     24(12), 1477-80; 1981&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of
     some 5H-benzo[a]phenoxazin-5-one derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Ueno, Yoshio; Maeda, Keiichi; Koshitani,
     Jinya; Yoshida, Takatoshi. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Heterocyclic Chemistry, 19(1), 189-91; 1982&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reaction of
     2,3-dichloro-5-hydroxy-1,4-naphthoquinone with aniline.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kolesnikov, V. T.; Belitskaya, L. D.;
     Litvin, B. L.&amp;nbsp; &amp;nbsp;&amp;nbsp;L&#39;vov. Politekh. Inst.,&amp;nbsp; &lt;st1:city w:st=&quot;on&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;Lvov&lt;/st1:place&gt;&lt;/st1:city&gt;,
     &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Zhurnal
     Organicheskoi Khimii, 18(4), 901; 1982&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chemistry of
     azidoquinones. Synthesis and thermolysis of the azido-o-quinone
     3-azido-4-(4-methylcyclohexa-3,6-dione-1,4-dienyl)-1,2-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Lee, Steward P.; Moore, Harold W. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Heterocycles, 19(11),
     2019-25; 1982&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of
     2,3-diamino-1,4-naphthoquinone derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Shishkina, R. P.; Ektova, L. V.;
     Matoshina, K. I.; Fokin, E. P. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Izvestiya Sibirskogo Otdeleniya Akademii Nauk
     SSSR, Seriya Khimicheskikh Nauk,&amp;nbsp;
     (5), 136-42; 1982&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Angular
     heterocycles:&amp;nbsp; synthesis of some
     substituted p-methoxyanilino-12H-benzo[a]phenothiazines.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Oberoi, G. K.; Agrawal, Rekha; Mital, R.
     L. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Indian
     Journal of Chemistry, Section B:&amp;nbsp;
     Organic Chemistry Including Medicinal Chemistry, 21B(6), 584-5;
     1982&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of
     2,3,5-triamino-1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Vasil&#39;eva, E. M.; Kolesnikov, V. T.;
     Dzikh, &lt;st1:place w:st=&quot;on&quot;&gt;I.&lt;/st1:place&gt; P. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Zhurnal Organicheskoi Khimii,
     18(10), 2228-9; 1982&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Ring closure in
     quinonylmethane dyes and merocyanine analogs. 6. Reactivity of the cyclohexyl
     moiety in
     2-chloro-3-[(1-cyclohexyl-6-fluoro-3-methyl-1H-quinoxalin-2-ylidene)methyl]-1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Schelz, Dieter; Rotzler, Niklaus. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Helvetica Chimica
     Acta, 65(7), 1990-5; 1982&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of
     7,10-disubstituted benzo[b]phenazine-6,11-quinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Nakazumi, Hiroyuki; Kondo, Kazuyoshi;
     Kitao, Teijiro.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis,&amp;nbsp; (10), 878-9; 1982&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Arylation of
     cyclic guanidine analogs with &lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; -haloanthraquinones:&amp;nbsp; new anthrapyrimidines.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Adam, Jean Marie; Winkler, Tammo; Rihs,
     Grety. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Helvetica
     Chimica Acta, 65(7), 2318-25; 1982&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naphthoquinone
     coloring matters.&amp;nbsp; Part 5.&amp;nbsp; Reactions of N,N-dialkylarylamines with
     1,4-naphthoquinones.&amp;nbsp; A convenient
     route to 2-(4-N,N-dialkylaminoaryl)-1,4-naphthoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;&lt;st1:place w:st=&quot;on&quot;&gt;Blackburn&lt;/st1:place&gt;,
     Christopher; Griffiths, John. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Chemical Research, Synopses,&amp;nbsp; (12), 320-1; 1982&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of
     naphthofuran-3-spirocyclohexanetriones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Hudson, Alan T.; Pejther, Michael
     J.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of the Chemical Society,
     Perkin Transactions 1:&amp;nbsp; Organic and
     Bio-Organic Chemistry (1972-1999),&amp;nbsp;
     (1), 35-7; 1983&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Nucleophilic
     arylation of derivatives of naphtho- and anthraquinones by
     2,6-di-tert-butylphenol.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Russkikh, S. A.; Klimenko, L. S.; Fokin,
     E. P. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Zhurnal
     Organicheskoi Khimii, 19(1), 158-64; 1983&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;A convenient
     synthesis of 2,3-dichloro-1,4-naphthoquinone-1-14C using a novel
     chlorination procedure.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Ehler, Kenneth W.; Pardini, Ronald S. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Organic Preparations
     and Procedures International, 15(3), 157-60; 1983&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reaction
     mechanism of one-pot synthesis of polycyclic quinones - direct evidence of
     a photoinduced electron-transfer process.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Maruyama, Kazuhiro; Tai, Seiji; Otsuki,
     Tetsuo. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chemistry
     Letters,&amp;nbsp; (6), 843-4; 1983&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Preparation of
     2-alkyl-1,4-naphthoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Peet, William G.; Tam, &lt;st1:city w:st=&quot;on&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;Wilson&lt;/st1:place&gt;&lt;/st1:city&gt;. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of the Chemical Society,
     Chemical Communications,&amp;nbsp; (15),
     853-4; 1983&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Angular
     heterocycles.&amp;nbsp; Utilization of
     arylaminonaphthoquinones in the synthesis of benzophenothiazines.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Agarwal, Nand L.; Atal, Chand K. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of
     Heterocyclic Chemistry, 20(6), 1741-4; 1983&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;N-Substituted
     enaminones from 3-aminobutenoic acids and 1,4-naphthoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Parr, Rodney W.; Reiss, James A. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Australian Journal of
     Chemistry, 37(2), 389-94; 1984&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naphthoquinone antipsoriatic agents.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Jones, Gordon H.; Young, John M. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;U.S., 4442127, 10 Apr
     1984&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;The fungicidal
     activity of substituted 1,4-naphthoquinones.&amp;nbsp; Part II:&amp;nbsp;
     alkoxy, phenoxy and acryloxy derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Clark, Nigel G.&amp;nbsp;&amp;nbsp;&amp;nbsp; Wye Coll., Ashford&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Pesticide Science&amp;nbsp; (1984),&amp;nbsp;
     15(3),&amp;nbsp; 235-40.&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/b&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;A new method of
     &lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;
     -ketoalkyl chain introduction into 1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Maruyama, Kazuhiro; Otsuki, Tetsuo; Tai,
     Seiji.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;Chemistry Letters&amp;nbsp; (1984),&amp;nbsp;&amp;nbsp;
     (3),&amp;nbsp; 371-4.&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/b&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;2,3-Bis(1,1-diphenylhydrazino)-5-hydroxy-1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kolesnikov, V. T.; Litvin, B. L.; Belitskaya,
     L. D. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Vestnik
     L&#39;vovskogo Politekhnicheskogo Instituta, 181, 68-70; 1984&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/b&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Study of
     1,4-naphthoquinone.&amp;nbsp; VIII.&amp;nbsp; Nucleophilic substitution in a series of
     2,3-dichloro-5-hydroxy-1,4-naphthoquinone and its derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Belitskaya, L. D.; Kolesnikov, V.
     T.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Zhurnal Organicheskoi
     Khimii&amp;nbsp; (1984),&amp;nbsp; 20(9),&amp;nbsp;
     1920-5.&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Izvestiya Akademii Nauk SSSR,
     Seriya Khimicheskaya,&amp;nbsp; (4), 855-7;
     1985&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Novel syntheses
     of phenoselenazinequinone infrared dyes.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kim, Sung Hoon; Matsuoka, Masaru; Kitao,
     Teijiro.&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chemistry Letters,&amp;nbsp; (9), 1351-2; 1985&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Novel syntheses
     of quinone-type IR dyes for optical recording media.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Matsuoka, Masaru; Kim, Sung Hoon; Kitao,
     Teijiro. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal
     of the Chemical Society, Chemical Communications,&amp;nbsp; (17), 1195-6; 1985&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of
     some 11-substituted 6-chloro-12H-benzo[a]phenothiazin-5-ols.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Mital, R. L.; Gupta, C. L.; Taneja,
     Vineeta; Gupta, S. B., Mrs.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Indian Journal of
     Chemistry, Section B:&amp;nbsp; Organic
     Chemistry Including Medicinal Chemistry, 24B(5), 551-2; 1985&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Dimeric
     naphthoquinones.&amp;nbsp; XVI.&amp;nbsp; Synthesis of maritinone and other
     8,8&#39;-bijuglones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Laatsch, Hartmut. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Liebigs Annalen der
     Chemie,&amp;nbsp; (12), 2420-42; 1985&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and
     photolysis of 2-chloro-1,4-naphthoquinone piperazino derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Shishkina, R. P.; Berezhnaya, V. N.; Fokin,
     E. P.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Izvestiya Akademii Nauk SSSR,
     Seriya Khimicheskaya,&amp;nbsp; (10), 2332-7;
     1985&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reaction of
     6-sulfonyl derivatives of 2,3-dichloro-1,4-naphthoquinone with
     nucleophilic reagents.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Shishkina, R. P.; Mamatyuk, V. I.;
     Ektova, L. V.; Fokin, E. P. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya,&amp;nbsp; (11), 2524-30; 1985&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Crown ethers
     based on 1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Markovskii, L. N.; Kal&#39;chenko, V. I.;
     Kartoflitskaya, A. P.; Kolesnikov, V. T. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Zhurnal Organicheskoi Khimii,
     21(7), 1501-6; 1985&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Photoinduced
     electron-transfer-initiated aromatic cyclization.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Maruyama, Kazuhiro; Otsuki, Tetsuo; Tai,
     Seiji. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal
     of Organic Chemistry, 50(1), 52-60; 1985&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Heterocyclic
     quinones.&amp;nbsp; XIII.&amp;nbsp; Reaction of thioamides with
     2,3-dichloro-1,4-naphthoquinone.&amp;nbsp; A
     novel synthesis of naphtho[2,3-d]thiazole-4,9-diones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Hammam, A. S.; Bayoumy, B. E. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Collection of
     Czechoslovak Chemical Communications, 50(1), 71-9; 1985&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Site-selective
     Diels-Alder reactions of 1,4,5,8-naphthodiquinones with anthracenes and
     successively with cyclopentadiene:&amp;nbsp;
     electronic effects vs. steric effects.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Hayakawa, Kenji; Aso, Mariko; Kanematsu,
     Ken. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal
     of Organic Chemistry, 50(12), 2036-40; 1985&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Quinone-amine
     reactions, XII.&amp;nbsp; Synthesis and color
     of naphthothiazinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kallmayer, Hans Joerg; Seyfang,
     Karlheinz. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Archiv der Pharmazie (&lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:city w:st=&quot;on&quot;&gt;Weinheim&lt;/st1:city&gt;,
      &lt;st1:country-region w:st=&quot;on&quot;&gt;Germany&lt;/st1:country-region&gt;&lt;/st1:place&gt;),
     318(4), 360-3; 1985&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Acyloxynaphthalene
     antipsoriatic agents.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Jones, Gordon H.; Venuti, Michael C.;
     Young, John M.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Eur. Pat. Appl.,
     146145, 26 Jun 1985&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Sulfonation and
     sulfochlorination of 2,3-dichloro-1,4-naphthoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Shishkina, R. P.; Mamatyuk, V. I.;
     Fokin, E. P. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya,&amp;nbsp; (4), 855-7; 1985&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;2,3-Dichloro-1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Suzuki, Hisashi; Yabe, Hirota. .&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Jpn. Kokai Tokkyo Koho,
     61018742, 27 Jan 1986, Showa&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Fluorinated quinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kaieda, Osamu; Hirota, Koichi; Itoh,
     Hideki; Awashima, Masaru; Nakamura, Toshiaki. Eur. Pat. Appl.&amp;nbsp; (1986), EP170190; JP&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; 61036240; US&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; 4689179.&lt;b&gt; &lt;/b&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Streptonigrin.&amp;nbsp; 1.&amp;nbsp;
     Structure-activity relationships among simple bicyclic
     analogs.&amp;nbsp; Rate dependence of DNA
     degradation on quinone reduction potential.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Shaikh, Iftikhar A.; Johnson, Francis;
     Grollman, Arthur P.&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;Journal of
     Medicinal Chemistry (1986), 29(8),&amp;nbsp;
     1329-40.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Topical nonsteroidal antipsoriatic
     agents.&amp;nbsp; 1.&amp;nbsp; 1,2,3,4-Tetraoxygenated naphthalene
     derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Jones, Gordon H.; Venuti, Michael C.;
     Young, John M.; Murthy, D. V. Krishna; Loe, Brad E.; Simpson, Richard A.;
     Berks, Andrew H.; Spires, Doreen A.; Maloney, Patrick J.; et al.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Medicinal Chemistry
     (1986),&amp;nbsp; 29(8),&amp;nbsp; 1504-11.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Quinone-amine reactions.&amp;nbsp; XVI:&amp;nbsp;
     synthesis and properties of 2- and/or 3-substituted
     benzoquinoxalinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kallmayer, Hans Joerg; Seyfang,
     Karlheinz.&amp;nbsp;&amp;nbsp;&amp;nbsp; Archiv der Pharmazie
     (1986),&amp;nbsp; 319(1),&amp;nbsp; 52-60.&lt;b&gt; &lt;/b&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Syntheses of some binaphthalenes.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Bajt, Oliver; Medja, Zdenka; Polanc,
     Slovenko; Tisler, Miha; Koller, Joze &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Croatica Chemica Acta&amp;nbsp; (1986),&amp;nbsp;
     Volume Date 1985,&amp;nbsp;
     58(4),&amp;nbsp; 745-55.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Studies of 1,4-naphthoquinones. IX.
     Semidine and prototropic rearrangements in the reaction of
     1,1-diphenylhydrazine with naphthoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Litvin, B. L.; Kolesnikov, V. T.;
     Kopel&#39;tsiv, Yu. A.; Yarish&lt;b&gt; &lt;/b&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of quinone-capped porphyrins
     by porphyrin self-photosensitized reaction.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Osuka, Atsuhiro; Furuta, Hiroyuki; Maruyama,
     Kazuhiro.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chemistry
     Letters&amp;nbsp; (1986),&amp;nbsp;&amp;nbsp; (4),&amp;nbsp;
     479-82.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;b&gt;1,4-Napthoquinones,
     XV: Reaction of 2- and 3-chloro or bromojuglone derivatives with
     methanolic alkali (Part 1: monomeric compounds).&lt;/b&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Wurm, Gotthard; Gurka, Hans Joachim;
     Geres, Uwe.&amp;nbsp; &amp;nbsp;&amp;nbsp;Archiv der Pharmazie (&lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:city w:st=&quot;on&quot;&gt;Weinheim&lt;/st1:city&gt;, &lt;st1:country-region w:st=&quot;on&quot;&gt;Germany&lt;/st1:country-region&gt;&lt;/st1:place&gt;)&amp;nbsp; (1986),&amp;nbsp;
     319(12),&amp;nbsp; 1106-13.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Zhurnal Organicheskoi Khimii&amp;nbsp; (1986),&amp;nbsp;
     22(1),&amp;nbsp; 140-6. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Multistep reversible redox
     systems.&amp;nbsp; XLVI.&amp;nbsp; N,N&#39;-Dicyanoquinonediimines, a new class
     of compounds.&amp;nbsp; I.&amp;nbsp; Synthesis and general properties.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Aumueller, Alexander; Huenig,
     Siegfried.&amp;nbsp;&amp;nbsp;&amp;nbsp; Liebigs Annalen der
     Chemie&amp;nbsp; (1986),&amp;nbsp;&amp;nbsp; (1),&amp;nbsp;
     142-64.&lt;b&gt; &lt;/b&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;1,4-Anthraquinonoid dienophiles
     applicable to synthesis of linear tetracycles.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Cameron, Donald W.; Conn, Costa;
     Crossley, Maxwell J.; Feutrill, Geoffrey I.; Fisher, Mark W.; Griffiths,
     Peter G.; Merrett, Bryan K.; Pavlatos, Dennis.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron Letters&amp;nbsp; (1986),&amp;nbsp;
     27(21),&amp;nbsp; 2417-20.&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of benzophenothiazinone
     derivatives from 2,3,5-trisubstituted 1,4-naphthoquinones with
     2-aminothiophenol.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Nanya, Seiko; Maekawa, Eturo; Kang, Wen
     Bing; Ueno, Yoshio.&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of
     Heterocyclic Chemistry&amp;nbsp; (1986),&amp;nbsp; 23(2),&amp;nbsp;
     589-92.&amp;nbsp; &lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Quinone-amine reactions.&amp;nbsp; XXI.&amp;nbsp;
     Photoreactivity of 2-amino-3-halo-1,4-naphthoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kallmayer, Hans Joerg; Tappe, Christiane.&amp;nbsp;&amp;nbsp;&amp;nbsp; Archiv der Pharmazie (1986),
     319(9),&amp;nbsp; 791-8.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of naphthoquinone
     derivatives. XII. Synthesis of naphtho[2,3-d]thiazole-4,9-dione
     derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Nakamori, Tateo; &lt;st1:place w:st=&quot;on&quot;&gt;Kasai&lt;/st1:place&gt;,
     Toshiyasu.&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;st1:place w:st=&quot;on&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Nippon&lt;/span&gt;&lt;/st1:place&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Kagaku Kaishi&amp;nbsp; (1986),&amp;nbsp;&amp;nbsp;
     (8),&amp;nbsp; 1091-5.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;A new type of angular phenothiazine
     ring system.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Okafor, Charles O.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron&amp;nbsp; (1986),&amp;nbsp;
     42(10),&amp;nbsp; 2771-5.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;b&gt;1,4-Naphthoquinones.&amp;nbsp; X.&amp;nbsp;
     Reaction of chloro derivatives of 2(5)-amino-1,4-naphthoquinone
     with 4-amino-2,2,6,6-tetramethylpiperidine and N-methylpiperazine.&lt;/b&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Litvin, B. L.; Kolesnikov, V. T.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Zhurnal Organicheskoi
     Khimii&amp;nbsp; (1986),&amp;nbsp; 22(8),&amp;nbsp;
     1736-42.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Photoallylation of quinones with
     allylstannane.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Maruyama, Kazuhiro; Imahori, Hiroshi;
     Osuka, Atsuhiro; Takuwa, Akio; Tagawa, Hiroyuki. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chemistry Letters (1986),&amp;nbsp;&amp;nbsp; (10), 1719-22.&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Heterocyclic quinonoid chromophoric
     systems: Part VII. Reaction of 2,3-dichloro-1,4-naphthoquinone with
     nitromethane and vinylogously substituted nitromethanes, di- and
     trinitrotoluenes.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Ayyangar, N. R.; Lugade, A. G.;
     Rajadhyaksha, M. N.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Indian Journal of
     Chemistry, Section B:&amp;nbsp; Organic
     Chemistry Including Medicinal Chemistry&amp;nbsp;
     (1986),&amp;nbsp; 25B(11),&amp;nbsp; 1126-32.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;Synthesis of
     11-aza-5H-benzophenoxazin-5-one and 11-aza-5H-pyridophenoxazin-5-one
     derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Nan&#39;ya, Seiko; Maekawa, Eturo; Kang, Wen
     Bing; Ueno, Yoshio.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of
     Heterocyclic Chemistry&amp;nbsp; (1986),&amp;nbsp; 23(6),&amp;nbsp;
     1697-700.&lt;b&gt; &lt;/b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of 1- and 4-substituted
     5H-benzo[a]phenoxazin-5-ones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Hayakawa, Hitoshi; Nanya, Seiko;
     Yamamoto, Tetsuo; Maekawa, Eturo; Ueno, Yoshio.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Heterocyclic
     Chemistry&amp;nbsp; (1986),&amp;nbsp; 23(6),&amp;nbsp;
     1737-40.&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naphthalene antipsoriatic and
     antiinflammatory agents and lipoxygenase inhibitors and a process for
     making them.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;st1:place w:st=&quot;on&quot;&gt;Krishna&lt;/st1:place&gt;
     Murthy, Dodballapur Venkataramiah; Young, John M.; Venuti, Michael C.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Eur.
     Pat. Appl., 215622, 25 Mar 1987&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;b&gt;&lt;a href=&quot;http://xlink.rsc.org/?DOI=C39870000359&quot; title=&quot;Select to access full content for this article (DOI:10.1039/C39870000359)&quot;&gt;An
     efficient photochemical synthesis of conformationally restricted
     quinone-substituted porphyrins&lt;/a&gt;&lt;/b&gt;&amp;nbsp;
     Osuka, Atsuhiro; Morikawa, Soichi; Maruyama, Kazuhiro; Hirayama, Satoshi;
     Minami, Takaaki &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;Journal of the Chemical Society, Chemical
     Communications,&amp;nbsp; (5), 359-61; 1987&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Photoinduced
     Substitution Reaction Initiated by Electron-Transfer. Photochemical
     Reaction of 2,3-Dichloro-1,4-naphthoquinone with Thiophenes&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;
     &amp;nbsp; Maruyama, Kazuhiro; &amp;nbsp;Tamiaki,&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Hitoshi
     &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;Bulletin
     of the Chemical Society of Japan, 60(5), 1847-51; 1987&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Preparation of
     5-hydroxynaphtho[2,3-d]thiazole-4,9-dione as medical bactericide.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Nishino, Isao; Kimura, Harutaka.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Jpn.
     Kokai Tokkyo Koho, 62234076, 14 Oct 1987, Showa&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Preparation of
     5-hydroxynaphtho[2,3-d]thiazole-4,9-dione as a veterinary bactericide.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Nishino, Isao; Kimura, Harutaka; Araki,
     Seiichi&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;Jpn. Kokai Tokkyo Koho, 62234019, 14 Oct 1987, Showa&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Some novel
     quinone-type dyes containing naphthoquinone and related fused ring
     systems.&amp;nbsp;&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;br /&gt;
     &amp;nbsp;Katritzky, Alan R.; Fan,&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Wei-Qiang&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Heterocyclic Chemistry, 25(3), 901-6; 1988&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Angular
     heterocycles. A convenient synthesis of azabenzophenothiazines. &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Kang,
     W. B.; Nan&#39;ya, Seiko;&amp;nbsp; Maekawa, Etur&lt;img alt=&quot;ocaron&quot; border=&quot;0&quot; height=&quot;12&quot; src=&quot;file:///C:/Users/hardesh/AppData/Local/Temp/msohtmlclip1/01/clip_image001.gif&quot; v:shapes=&quot;_x0000_i1025&quot; width=&quot;8&quot; /&gt;; Ueno, Yoshio&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal
     of Heterocyclic Chemistry, 25(1), 113-17; 1988&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Revue Roumaine de Chimie,
     33(3), 291-3; 1988&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.sciencedirect.com/science?_ob=ArticleURL&amp;amp;_udi=B6THR-43CCC9D-N&amp;amp;_user=10&amp;amp;_coverDate=12%2F31%2F1988&amp;amp;_alid=1065854786&amp;amp;_rdoc=2&amp;amp;_fmt=high&amp;amp;_orig=search&amp;amp;_cdi=5289&amp;amp;_sort=r&amp;amp;_docanchor=&amp;amp;view=c&amp;amp;_ct=2&amp;amp;_acct=C000050221&amp;amp;_version=1&amp;amp;_urlVersion=0&amp;amp;_userid=10&amp;amp;md5=14f852a908675e4ae25e308ffe2b7ac1&quot;&gt;The
     first branched benzoxazinophenothiazine ring system and its aza-analogues&lt;/a&gt;
     &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Okafor,&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Charles O. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron, 44(4), 1187-94; 1988&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3;&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Nippon&lt;/span&gt;&lt;/st1:place&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Kagaku Kaishi,&amp;nbsp; (5),
     743-51; 1988&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Nippon&lt;/span&gt;&lt;/st1:place&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Kagaku Kaishi,&amp;nbsp; (5),
     752-62; 1988&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Jpn. Kokai Tokkyo Koho,
     63150273, 22 Jun 1988, Showa&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bridged cyanine dyes. Part 2 . 1-(&lt;i&gt;N&lt;/i&gt;-methyl-2-benzothiazolylinio)-3-(&lt;i&gt;N&lt;/i&gt;-methyl-2-benzothiazolylene)
     and 1-(&lt;i&gt;N&lt;/i&gt;-methyl-4-pyridinio)-3-(&lt;i&gt;N&lt;/i&gt;-methyl-4-pyridylene)cyclopenta-1,4-dienes
     with fused rings. &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Katritzky, Alan
     R.; Liang, De-Sheng; Fan&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Wei-Qiang &amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Heterocyclic Chemistry, 25(5), 1315-19; 1988&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt;A new
     synthesis of ‘three-branched’ diazaphenothiazine dyes.&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;color: black; display: none; font-size: 10pt; line-height: 150%;&quot;&gt;&lt;br /&gt;
     &lt;br /&gt;
     &lt;br /&gt;
     References and further reading may be available for this article. To view
     references and further reading you must &lt;a href=&quot;http://www.sciencedirect.com/science?_ob=ArticleURL&amp;amp;_udi=B6TFY-44W52BT-3&amp;amp;_user=10&amp;amp;_coverDate=12%2F31%2F1988&amp;amp;_alid=1065960786&amp;amp;_rdoc=1&amp;amp;_fmt=full&amp;amp;_orig=search&amp;amp;_cdi=5239&amp;amp;_sort=r&amp;amp;_docanchor=&amp;amp;view=c&amp;amp;_ct=1&amp;amp;_acct=C000050221&amp;amp;_version=1&amp;amp;_urlVersion=0&amp;amp;_userid=10&amp;amp;md5=9c78346c377c4175eed4b2855bb1d545&quot;&gt;purchase&lt;/a&gt;
     this article.&lt;/span&gt;&lt;span style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;span style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt;Okafor, Charles O.; Okoro,&lt;/span&gt;&lt;span style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;span style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt;Uche C.&lt;b&gt; &amp;nbsp;&lt;/b&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Dyes and Pigments, 9(6), 427-42; 1988&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Zhurnal Obshchei Khimii, 58(10), 2377-83; 1988&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt;[2 + 4] Photocyclization
     between quinones and allenes via photoinduced electron transfer&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: #333333; font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Maruyama, Kazuhiro;&amp;nbsp;Imahori,&lt;b&gt; &lt;/b&gt;Hiroshi&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: #333333; font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Organic Chemistry, 54(11), 2692-702; 1989.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Khimiya
     Geterotsiklicheskikh Soedinenii,&amp;nbsp;
     (12), 1683-7; 1987&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;Indian Journal of Chemistry, Section
     B:&amp;nbsp; Organic Chemistry Including
     Medicinal Chemistry, 28B(1), 69-70; 1989&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt;Allylation of Quinones via Photoinduced Electron-Transfer
     Reactions from Allylstannanes.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt; Maruyama, Kazuhiro; Imahori, Hiroshi&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Bulletin
     of the Chemical Society of &lt;st1:country-region w:st=&quot;on&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;Japan&lt;/st1:place&gt;&lt;/st1:country-region&gt;,
     62(3), 816-25; 1989&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Khimiya
     Geterotsiklicheskikh Soedinenii,&amp;nbsp;
     (1), 66-8; 1989&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.sciencedirect.com/science?_ob=ArticleURL&amp;amp;_udi=B6THR-42G789M-8T&amp;amp;_user=10&amp;amp;_coverDate=12%2F31%2F1989&amp;amp;_alid=1065857997&amp;amp;_rdoc=1&amp;amp;_fmt=high&amp;amp;_orig=search&amp;amp;_cdi=5289&amp;amp;_sort=r&amp;amp;_docanchor=&amp;amp;view=c&amp;amp;_ct=1&amp;amp;_acct=C000050221&amp;amp;_version=1&amp;amp;_urlVersion=0&amp;amp;_userid=10&amp;amp;md5=619472021da1117b0a8a28a4cd71f3b5&quot;&gt;&lt;b&gt;Quinone-linked
     and quinone-capped porphyrins. Their one-pot photochemical synthesis and
     fluorescence behavior&lt;/b&gt;&lt;/a&gt; Osuka, Atsuhiro; Maruyama, Kazuhiro; Hirayama,&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Satoshi &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron,
     45(15), 4815-29; 1989&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Novel chromophoric heterocycles based on maleimide and naphthoquinones.&amp;nbsp;&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Katritzky, Alan R.; Fan, Wei-Qiang; Li, Qiao-Ling;
     Bayyuk&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;, &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Shibli&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Journal of Heterocyclic
     Chemistry, 26(4), 885-92; 1989&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Khimiko-Farmatsevticheskii
     Zhurnal, 23(12), 1485-8; 1989&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Novel dyestuffs containing dicyanomethylidene groups.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Katritzky, Alan R.; Fan, Wei-Qiang; Liang, De-Sheng;
     Li&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Qiao-Ling
     &amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal
     of Heterocyclic Chemistry, 26(6), 1541-5; 1989&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;/span&gt;&lt;b&gt;&lt;span style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt;Von der
     variantenreichen Chemie des Chinoxalins zu chinoiden und indigoiden
     Chromophoren : IV. Die Chemie der Naphtho-, Chinolino- und
     Anthracenophenazinone&lt;/span&gt;&lt;/b&gt;&lt;a href=&quot;http://www.blogger.com/blogger.g?blogID=7775904593195892177&quot; name=&quot;bfnfn1&quot;&gt;&lt;/a&gt;&lt;b&gt;&lt;span style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;color: black; display: none; font-size: 10pt; line-height: 150%;&quot;&gt;&lt;br /&gt;
     &lt;br /&gt;
     &lt;br /&gt;
     References and further reading may be available for this article. To view
     references and further reading you must &lt;a href=&quot;http://www.sciencedirect.com/science?_ob=ArticleURL&amp;amp;_udi=B6TFY-43PS71N-7V&amp;amp;_user=10&amp;amp;_coverDate=12%2F31%2F1990&amp;amp;_alid=1065954310&amp;amp;_rdoc=1&amp;amp;_fmt=full&amp;amp;_orig=search&amp;amp;_cdi=5239&amp;amp;_sort=r&amp;amp;_docanchor=&amp;amp;view=c&amp;amp;_ct=1&amp;amp;_acct=C000050221&amp;amp;_version=1&amp;amp;_urlVersion=0&amp;amp;_userid=10&amp;amp;md5=9f6f62d3392fed1875c15eda2ff87ddb&quot;&gt;purchase&lt;/a&gt;
     this article&lt;/span&gt;&lt;span style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt; Schelz, Dieter&lt;/span&gt;&lt;span style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Dyes
     and Pigments, 12(1), 1-20; 1990&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.sciencedirect.com/science?_ob=ArticleURL&amp;amp;_udi=B6THS-42HFVS6-G1&amp;amp;_user=10&amp;amp;_coverDate=12%2F31%2F1989&amp;amp;_alid=1065859681&amp;amp;_rdoc=1&amp;amp;_fmt=high&amp;amp;_orig=search&amp;amp;_cdi=5290&amp;amp;_sort=r&amp;amp;_docanchor=&amp;amp;view=c&amp;amp;_ct=1&amp;amp;_acct=C000050221&amp;amp;_version=1&amp;amp;_urlVersion=0&amp;amp;_userid=10&amp;amp;md5=60738a034d4b6625bcaf155576f7e9a2&quot;&gt;Dichloro
     quinones as dienophiles: synthesis of alizarin derivatives&lt;/a&gt;&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Cameron,
     Donald W.; Feutrill, Geoffrey I.; Keep, &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Philip L. C. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron Letters, 30(38), 5173-6; 1989&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Novel
     Photocyclization between Quinone and 1,1-Diphenylcyclopropane &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.jstage.jst.go.jp/search/?typej=on&amp;amp;typep=on&amp;amp;typer=on&amp;amp;d3=au&amp;amp;dp3=Kazuhiro+Maruyama&amp;amp;ca=999999&amp;amp;alang=all&amp;amp;rev=all&amp;amp;pl=20&amp;amp;search=%8C%9F%8D%F5%8E%C0%8Ds&quot;&gt;&amp;nbsp;Maruyama&lt;/a&gt;,&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Kazuhiro; &lt;a href=&quot;http://www.jstage.jst.go.jp/search/?typej=on&amp;amp;typep=on&amp;amp;typer=on&amp;amp;d3=au&amp;amp;dp3=Hiroshi+Imahori&amp;amp;ca=999999&amp;amp;alang=all&amp;amp;rev=all&amp;amp;pl=20&amp;amp;search=%8C%9F%8D%F5%8E%C0%8Ds&quot;&gt;Imahori&lt;/a&gt;,&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Hiroshi; &lt;a href=&quot;http://www.jstage.jst.go.jp/search/?typej=on&amp;amp;typep=on&amp;amp;typer=on&amp;amp;d3=au&amp;amp;dp3=Yoshiki+Ozawa&amp;amp;ca=999999&amp;amp;alang=all&amp;amp;rev=all&amp;amp;pl=20&amp;amp;search=%8C%9F%8D%F5%8E%C0%8Ds&quot;&gt;&amp;nbsp;Ozawa&lt;/a&gt;,&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Yoshiki &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;Chemistry Letters,&amp;nbsp; (12), 2117-18; 1989&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of the Chemical
     Society, Perkin Transactions 2:&amp;nbsp;
     Physical Organic Chemistry (1972-1999), &amp;nbsp;(2), 257-65; 1990&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Izvestiya Sibirskogo
     Otdeleniya Akademii Nauk SSSR, Seriya Khimicheskikh Nauk,&amp;nbsp; (3), 46-50; 1990&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Kenkyu Hokoku - Asahi
     Garasu Kogyo Gijutsu Shoreikai, 55, 73-81; 1989&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and electrochemical properties of
     benzo[b]naphtho[2,3-e][1,4]-dioxin-6,11-quinones and their N,N&#39;-dicyano
     quinone diimine derivatives &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: #333333; font-size: 10pt; line-height: 150%;&quot;&gt;Czekanski,
     Tomasz;&amp;nbsp; Hanack, Michael;&amp;nbsp; Becker, James Y.;&amp;nbsp;&amp;nbsp;Bernstein,
     Joel; &amp;nbsp;&amp;nbsp;Bittner, Shmuel; &amp;nbsp;Kaufman-Orenstein, Leah;&amp;nbsp; Peleg;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: #333333; font-size: 10pt; line-height: 150%;&quot;&gt;Dina&amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Journal of Organic Chemistry, 56(4), 1569-73; 1991&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Khimiya
     Geterotsiklicheskikh Soedinenii,&amp;nbsp;
     (10), 1406-8; 1990&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Egyptian Journal of
     Chemistry, 1988, 31(1), 29-40; 1990&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of 3-substituted
     2-hydroxybenz[&lt;i&gt;f&lt;/i&gt;]indolequinones and benz[&lt;i&gt;f&lt;/i&gt;]isatinquinone - A
     new &lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;img alt=&quot;pi&quot; border=&quot;0&quot; height=&quot;9&quot; src=&quot;file:///C:/Users/hardesh/AppData/Local/Temp/msohtmlclip1/01/clip_image002.gif&quot; v:shapes=&quot;_x0000_i1026&quot; width=&quot;11&quot; /&gt;&lt;b&gt;-acceptor system.&lt;/b&gt;&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;
     Shakhnovich,&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;A. I. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Heterocyclic
     Chemistry, 28(1), 33-9; 1991&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Archiv der Pharmazie (&lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:city w:st=&quot;on&quot;&gt;Weinheim&lt;/st1:city&gt;, &lt;st1:country-region w:st=&quot;on&quot;&gt;Germany&lt;/st1:country-region&gt;&lt;/st1:place&gt;), 324(8), 491-5; 1991&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Kenkyu Hokoku - Asahi
     Garasu Zaidan, 56, 117-30; 1990&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt;Selenation of 1,5-Naphthoquinones: Novel Synthesis of
     Naphthopyridoselenazines&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt; Makoto
     Sakakibara&lt;sup&gt;1)&lt;/sup&gt;, Ishida, Tetsuya; Watanabe, Yoshihiko; &amp;nbsp;Toru, Takeshi; Ueno;&lt;sup&gt; &lt;/sup&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt;Yoshio &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;Bulletin of the Chemical Society of
     Japan, 64(7), 2242-8; 1991&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Jpn. Kokai Tokkyo Koho,
     03240782, 28 Oct 1991, Heisei&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Jpn. Kokai Tokkyo Koho,
     03246250, 01 Nov 1991, Heisei&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Chemical
     Research, Synopses,&amp;nbsp; (6), 184-5;
     1992&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.informaworld.com/smpp/content~db=all~content=a910150362&quot; title=&quot;Click to view this record&quot;&gt;Some Novel Quinone-Type Compounds
     Containing Arylseleno Groups Derived from Tetrachloro-1, 4-Benzoquinone
     and 2, 3-Dichloro-1, 4-Naphthoquinone&lt;/a&gt;&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;. Fan;&amp;nbsp; Wei-Qiang;
     Wang;&amp;nbsp; Jin; Jiang; Jinlong; Zhang,&lt;i&gt; &lt;/i&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Yong-Min &amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthetic
     Communications, 22(21), 3061-6; 1992&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.informaworld.com/smpp/content~db=all~content=a910150361&quot; title=&quot;Click to view this record&quot;&gt;Synthesis of Novel Naphthoquinone Fused
     1, 3-Dithioles&lt;/a&gt;&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;br /&gt;
     Fan,&amp;nbsp; Wei-Qiang; Ruan, Min-De;&amp;nbsp; Wang, Ping, Xin-;&amp;nbsp; Ye,
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&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Liebigs Annalen der
     Chemie,&amp;nbsp; (6), 695-7; 1993&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt;Design of antineoplastic agents on
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&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Yakhak Hoechi, 37(1),
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&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of Some Novel Naphthoquinone Fused Selenazoles
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&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Jpn. Kokai Tokkyo Koho,
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&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Youji Huaxue, 13(6),
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&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;The Influence of the Axial Chirality of
     Dibenzo[a,c]cyclooctene on the Configuration of Its Photo-Diels-Alder
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&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of the Chemical
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     Organic and Bio-Organic Chemistry (1972-1999),&amp;nbsp; (15), 2191-5; 1994&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Liebigs Annalen der
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&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Collection of
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&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chemical
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     Ming-De, Ruan; Hua-Rong, Zhao; Wei-Qiang, Fan; Xun-Jun,&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Zhou&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Journal of Organometallic
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&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.informaworld.com/smpp/content~db=all~content=a757063530&quot; title=&quot;Click to view this record&quot;&gt;A Novel Synthesis of Some
     Naphtho[2,3-d]Thiazole-4,9-Diones From Lawsone&lt;/a&gt;&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Brahmeshwari;&amp;nbsp;
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&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reaction of N&lt;sup&gt;1&lt;/sup&gt;,
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&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: black; font-size: 10pt; line-height: 150%;&quot;&gt;Use of Thiazyl Chlorides, Alkyl
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&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span class=&quot;title&quot;&gt;&lt;span lang=&quot;EN-US&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span class=&quot;title&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.mdpi.com/1420-3049/5/4/M160&quot;&gt;2-Chloro-3-(4-morpholino)-1,4-naphthoquinone&lt;/a&gt;&lt;/span&gt;&lt;/b&gt;&lt;/span&gt;&lt;span class=&quot;title&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;, &lt;/span&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;authors&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bhattacharyya,&lt;/span&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt; &lt;/span&gt;&lt;span class=&quot;authors&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;ukanta
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     thieno[2,3-d]pyrimidine derivatives containing sulfonamido moieties&lt;/a&gt;.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; El-Gaby, &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;M. S. A.&lt;i&gt; &lt;/i&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Phosphorus, Sulfur and Silicon and the Related Elements, 156,
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&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.thieme-connect.com/ejournals/abstract/synthesis/doi/10.1055/s-2000-6314&quot;&gt;Quinonic
     Enaminones; Synthesis of New Dialkylaminovinyl and Bis(dialkylaminovinyl)
     Derivatives of Quinones&lt;/a&gt;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Alnabari,
     Mohammad; Bittner, Shmuel &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis,&amp;nbsp; (8), 1087-1090; 2000&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of some new fluorinated
     phenothiazines.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Taneja, Vineeta Khatri nee; Garg, Urmila
     Gupta nee; Gorver, Vineeta Sareen nee; Sharma, Kanti.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Asian Journal of Chemistry&amp;nbsp; (2000),&amp;nbsp;
     12(4),&amp;nbsp; 1273-1276&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and
     radiation stability of novel biologically active sulfur compounds derived
     from 1,2-bis(4-amino-5-mercapto-s-triazol-3-yl)ethane.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;
     Ghorab, M. M.; El-Sharief, A. M. Sh.; Ammar, Y. A.; Mohamed, Sh. I &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Farmaco, 55(5), 354-361; 2000&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Heterocyclic dyes, their production and their use.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; Kaul, Bansi Lal; Piastra, Bruno; Wolf,
     Valerie. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;Eur. Pat. Appl., 1061103, 20
     Dec 2000&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Studies
     on the synthesis of some pyrazolo[1,5-a]pyrimidines bearing sulfonamido
     moieties.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;El-Gaby, Mohamed S. A.; Sayed, Ahmed Z.;
     Abu-Shanab, Fathi A.; Hussein, Abdel M.&amp;nbsp;&amp;nbsp;
     &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Phosphorus, Sulfur and Silicon and the
     Related Elements, 164, 1-10; 2000&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of
     some new fused and polyfused quinoxalines.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Abdel-Ghany, H. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Phosphorus,
     Sulfur and Silicon and the Related Elements, 164, 259-268; 2000&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chemistry of L-ascorbic acid. Part 3. Photoreduction of
     quinones with 5,6-O-isopropylidene-L-ascorbic acid.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kulkarni, Mukund G.; Kate, Sandesh
     D.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;Perkin 1,&amp;nbsp; (24),
     4242-4244; 2000&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of new sulfonamide drugs.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Mohamed, Shaaban
     Kamel.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;Afinidad, 57(490), 451-456; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;2000&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Some reactions with tetrahydropyrimidine-2-thione:
     synthesis of thiazolopyrimidine, pyranothiazolopyrimidine, and
     pyrimidothiazoloquinoxaline derivatives as anticancer agents.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Ismail, M. M. F. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Al-Azhar Journal of Pharmaceutical Sciences, 23, 1-10; 1999&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Heterocyclic dyes with condensed rings
     derived from 1,3-dihydro-2H-benzimidazole-2-thiones.
     Benzimidazo[2,1-b]naphtho[2,3-d]thiazole-7,12-diones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Raditoiu, Valentin; Wagner, Luminita;
     Raditoiu, Alina; Ardeleanu, Petrea; Grigoriu, Nicoleta; Tarabasanu-Mihaila,
     Corneliu. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Revista de Chimie (&lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:city w:st=&quot;on&quot;&gt;Bucharest&lt;/st1:city&gt;, &lt;st1:country-region w:st=&quot;on&quot;&gt;Romania&lt;/st1:country-region&gt;&lt;/st1:place&gt;),
     52(4), 199-205; 2001&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Chemistry,
     12(4), 1273-1276; 2000&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Amino acids in the synthesis of
     heterocyclic systems: The synthesis of triazinoquinazolinones,
     triazepinoquinazolinones and triazocinoquinazolinones of potential
     biological interest.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;El-Sharief, A. M. Sh.; Ammar, Y. A.;
     Zahran, M. A.; Ali, A. H.; El-Gaby, M. S. A.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Molecules
     [online computer file], 6(3), 267-278; 2001&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: navy; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;N,N-bis(quinonyl)amines; synthesis and
     X-ray structure.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     Bittner, S.; Meenakshi, C.; Temtsin, G.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron,
     57(34), 7423-7429; 2001&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: navy; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;Rhodium generated carbonyl ylides with
     p-quinones: synthesis of oxa-bridged polycyclic systems.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Muthusamy, S.; Babu, S. A.; Gunanathan,
     C.; Suresh, E.; Dastidar, P.; Jasra, R. V. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron,
     57(32), 7009-7019; 2001&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: navy; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of
     3-(benzotriazol-1-yl)naphthoquinone derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Ganushchak, N. I.; Romanyuk, A. L.;
     Litvin, B. L.; Lys, R. I.; Polishchuk, O. P. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Russian
     Journal of General Chemistry (Translation of Zhurnal Obshchei Khimii),
     71(2), 286-289; 2001&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;New quinone-amino acid conjugates
     linked via a vinylic spacer.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     Alnabari, Mohammad; Bittner, Shmuel. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.springerlink.com/content/l9rwnb135qcnh36m/fulltext.pdf&quot;&gt;Amino
     Acids, 20(4), 381-387; 2001&lt;/a&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis
     of organic third-order nonlinear optical materials of dioxonaphthothiazole
     and dibenzothianthrene compounds.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Gao,
     Jian-rong; Shen, Wei-guang; Cheng, Lu-bai; Chen, Xing.&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;st1:state w:st=&quot;on&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Zhejiang&lt;/span&gt;&lt;/st1:place&gt;&lt;/st1:state&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Gongye Daxue Xuebao, 28(1), 14-17; 2000&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Palladium-catalyzed cross coupling of arylboronic acids
     with 2-chloro-1,4-naphthoquinones: the synthesis of 2-aryl- and
     2,3-diaryl-1,4-naphthoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     Best, Wayne M.; Sims, Colette G.; Winslade, Merilyn. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;Australian Journal of Chemistry, 54(6), 401-404;
     2001&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis, electrochemical and spectral
     properties of some &lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;
     -N-quinonyl amino acids.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Bittner, S.; Gorohovsky, S.; Paz-Tal,
     O.; Becker, J. Y.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Amino Acids, 22(1), 71-93; 2002&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Novel heterocycles from creatinine.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Mourad, Aboul-Fetouh E.; Hassan, Alaa
     A.; Mohamed, Nasr K.; Aly, Ashraf A.; Ali, Bahaa A.&amp;nbsp;&amp;nbsp; &amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Heterocyclic Communications, 7(6), 541-548; 2001&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;Synthesis
     and electrochemical studies on a crown ether bearing a naphthoquinone
     acceptor.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Bond, Alan M.; Ghiggino, Kenneth P.;
     Hogan, Conor F.; Hutchison, James A.; Langford, Steven J.; Lygris, Emmanuel;
     Paddon-Row, Michael N. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Australian Journal of
     Chemistry, 54(12), 735-738; 2001&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Construction of fused cyclooctanoid
     ring systems via seven-membered ring carbonyl ylides.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Muthusamy, Sengodagounder; Babu,
     Srinivasarao Arulananda; Gunanathan, Chidambaram; Suresh, Eringathodi;
     Dastidar, Parthasarathi. Ammar, Y. A.; Ghorab, M. M.; El-Sharief, A. M.
     Sh.; Mohamed, Sh. I. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bulletin of the Chemical
     Society of Japan, 75(4), 801-811; 2002&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naproxen in
     heterocyclic chemistry: Novel syntheses of triazoles, triazolothiadiazines,
     triazolothiadiazoles, and triazolothiadiazepine bearing an asymmetric
     carbon atom and radiostability of the biologically active compounds.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;
     Ammar, Y. A.; Ghorab, M. M.;. El-Sharief, A. M. Sh; Mohamed,&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Sh. I. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Heteroatom
     Chemistry, 13(3), 199-206; 2002&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Regiocontrolled synthesis of the
     trimeric quinone framework of conocurvone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Emadi, Ashkan; Harwood, John S.;
     Kohanim, Sahar; Stagliano, Kenneth W. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Organic
     Letters, 4(4), 521-524; 2002 .&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Vicarious nucleophilic substitution of
     hydrogen (VNS) in 1,4-naphthoquinone derivatives-competition between VNS
     and vinylic nucleophilic substitution (SNV).&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Makosza, Mieczyslaw; Nizamov,
     Shamil.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron,
     57(47), 9615-9621; 2001.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of a new polypyridinic highly
     conjugated ligand with electron-acceptor properties.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Diaz, R.; Reyes, O.; Francois, A.;
     Leiva, A. M.; Loeb, B. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron Letters,
     42(37), 6463-6467; 2001.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Sonochemical chloro-oxidation of phenols using HCl-H2O2.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Bhatkhande, B. S.; Adhikari, M. V.;
     Samant, S. D.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;Ultrasonics Sonochemistry, 9(1), 31-35; 2002&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and antifungal activity of some new
     miscellaneous s-triazoles.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Ghorab, M. M.; El-Sharief, A. M. Sh.;
     Ammar, Y. A.; Mohamed, Sh. I. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Phosphorus, Sulfur
     and Silicon and the Related Elements, 173, 223-233; 2001&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of 2-alkoxy
     1,4-naphthoquinone derivatives as antiplatelet, antiinflammatory, and
     antiallergic agents.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Lien, Jin-Cherng; Huang, Li-Jiau; Teng,
     Che-Ming; Wang, Jih-Pyang; Kuo, Sheng-Chu. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chemical
     &amp;amp; Pharmaceutical Bulletin, 50(5), 672-674; 2002&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Efficient Synthesis of &#39;Redox-Switched&#39; Naphthoquinone
     Thiol-Crown Ethers and Their Biological Activity Evaluation.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Huang, Sheng-Tung; Kuo, Hsien-Shou;
     Hsiao, Chiao-Long; Lin, Yuh-Ling. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;Bioorganic &amp;amp; Medicinal Chemistry, 10(6), 1947-1952; 2002.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naturalization and modification of
     natural colors of flowers. I. Naphthofuroquinolinedione dyes.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Boscornea, Cristian; Pasolea, &lt;st1:place w:st=&quot;on&quot;&gt;Florin&lt;/st1:place&gt;; Tarabasanu Mihaila, Corneliu; Boscornea,
     Corina. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Revista de Chimie (&lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:city w:st=&quot;on&quot;&gt;Bucharest&lt;/st1:city&gt;, &lt;st1:country-region w:st=&quot;on&quot;&gt;Romania&lt;/st1:country-region&gt;&lt;/st1:place&gt;),
     53(5), 394-403; 2002&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;The synthesis of third-order optical
     nonlinear organic polyheterocyclic materials.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Gao, Jian Rong; Xiang, Bin; Shan, Wei
     Guang; Huang, Ming; Cheng, Lu Bai. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chinese
     Chemical Letters, 13(7), 609-612; 2002&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;Color reactions between trialkylamines
     and naphthoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kallmayer, H.-J.; Thierfelder, B.&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Pharmazie,
     57(7), 456-459; 2002(C and Br)&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reaction of
     2,3-dichloro-1,4-naphthoquinone with some active methylene compounds in
     different basic media.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Hammam, A. S.; Fandy, R. F.; Hassan, M.
     A.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chemistry
     of Heterocyclic Compounds (&lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:city w:st=&quot;on&quot;&gt;New
       York&lt;/st1:city&gt;, &lt;st1:state w:st=&quot;on&quot;&gt;NY&lt;/st1:state&gt;, &lt;st1:country-region w:st=&quot;on&quot;&gt;United States&lt;/st1:country-region&gt;&lt;/st1:place&gt;)(Translation of
     Khimiya Geterotsiklicheskikh Soedinenii), 38(4), 400-405; 2002&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;Reaction of some trialkylamine drugs with
     2,3-dichloro-1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kallmayer, H.-J.; Thierfelder, B.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Pharmazie,
     57(9), 648-649; 2002&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and photochemical behavior of
     donor-acceptor systems obtained from chloro-1,4-naphthoquinone attached to
     trans-aminostilbenes.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Sutovsky, Y.; Likhtenshtein, G. I.;
     Bittner, S.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron, 59(16), 2939-2945; 2003&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reactions
     between isopropyl-alkylamines and 2,3-dichloro-1,4-naphthoquinone and
     2,3-dichloro-1,4-naphthoquinone/acetaldehyde.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kallmayer, H.-J.; Thierfelder, B.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Pharmazie,
     58(2), 104-107; 2003&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;An efficient and facile synthesis of
     substituted cinnoline and benzo[h]cinnoline derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Gomaa, Mohsen Abdel-Motaal. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron Letters, 44(17), 3493-3496; 2003.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Some new nitrogen bridgehead
     heterocyclic quinone cyanine dyes.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Koraiem, A. I. M.; El-Maghraby, M. A.;
     Abu-El-Hamd, R. M.; Gomaa, M. M.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;st1:city w:st=&quot;on&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Aswan&lt;/span&gt;&lt;/st1:place&gt;&lt;/st1:city&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Science &amp;amp; Technology Bulletin, 21, 8-21; 2002&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and cytotoxicity evaluation
     of 2-amino- and
     2-hydroxy-3-ethoxycarbonyl-N-substituted-benzo[f]indole-4,9-dione
     derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Lee, Hyun-Jung; Suh, Myung-Eun; Lee,
     Chong-Ock.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bioorganic &amp;amp; Medicinal Chemistry, 11(7), 1511-1519; 2003.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and cytotoxicity of
     6,11-Dihydro-pyrido- and 6,11-Dihydro-benzo[2,3-b]phenazine-6,11-dione
     derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Kim, Young-Shin; Park, Se-Young; Lee,
     Hyun-Jung; Suh, Myung-Eun; Schollmeyer, Dieter; Lee, Chong-Ock. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bioorganic &amp;amp; Medicinal Chemistry, 11(8), 1709-1714; 2003.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reaction of benzoquinones and naphthoquinones with
     1,8-diamino-3,6-dioxanonane and with 1,11-diamino-3,6,9-trioxaundecane.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Machocho, Alex K.; Win, Thida; Grinberg,
     Sarina; Bittner, Shmuel. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron
     Letters, 44(29), 5531-5534; 2003&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Epoxidation of quinones with urea hydrogen peroxide.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Valderrama, Jaime A.; Gonzalez, M.
     Florencia; Torres, Cristian. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;Heterocycles,
     60(10), 2343-2348; 2003&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Study of a
     reaction between 2,3-dichloro-1,4-naphthoquinone and N,N&#39;-diphenyl
     thiourea involving an EDA adduct as intermediate.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Datta, Kakali; Mukherjee, Asok K. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Spectrochimica Acta, Part A: Molecular and Biomolecular
     Spectroscopy, 60A(7), 1641-1647; 2004&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;2-Oxiranecarbonitriles in the synthesis
     of linked quinono heterocyclic derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Volmajer, Julija; Toplak, Renata;
     Bittner, Shmuel; Majcen Le Marechal, Alenka. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://content.arkat-usa.org/ARKIVOC/JOURNAL_CONTENT/manuscripts/2003/BS-862AP%20as%20published%20mainmanuscript.pdf&quot;&gt;ARKIVOC
     (Gainesville, FL, United States),&amp;nbsp;
     (14), 49-61; 2003&lt;/a&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of original
     benzo[g]quinoxaline-5,10-diones by bis-SRN1 methodology.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Remusat, Vincent; Terme, Thierry;
     Gellis, Armand; Rathelot, Pascal; Vanelle, Patrice.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal
     of Heterocyclic Chemistry, 41(2), 221-225; 2004&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Effect of Methoxyl Group Position on
     the Regioselectivity of Ammonia Substitution Reactions Involving
     3,3&#39;-Dichloro-2,2&#39;-binaphthoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Stagliano, Kenneth W.; Lu, Zhenhai;
     Emadi, Ashkan; Harwood, John S.; Harwood, Cynthia A.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal
     of Organic Chemistry, 69(15), 5128-5131; 2004&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and biological activity of
     1,4-naphthoquinone derivatives, Part II.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Zoorob, H. H.; Berghot, M. A.;
     Abou-Elzahab, M. M.; Amer, F. A.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Mansoura Science Bulletin, A: Chemistry, 29(2), 129-142; 2002&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and
     cytotoxicity evaluation of pyridin[2,3-f]indole-2,4,9-trione and
     benz[f]indole-2,4,9-trione derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Lee, Hyun-Jung; Park, So-Young; Kim, Jin
     Sung; Song, Hyun Min; Suh, Myung-Eun; Lee, Chong-Ock.&amp;nbsp; &amp;nbsp;&amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bioorganic &amp;amp; Medicinal Chemistry, 11(22), 4791-4796; 2003&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis
     of naphtho[2,3-b]furan-4,9-diones having a trifluoromethyl group under
     conditions of phase-transfer catalysis.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Davydov, D. V.; Beletskaya, &lt;st1:place w:st=&quot;on&quot;&gt;I.&lt;/st1:place&gt; P. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Russian Journal of
     Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii), 40(1),
     134-136; 2004&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;DABCO-Assisted coupling of some
     activated olefins and 2,3-dihalo-1,4-naphthoquinones and conversion to the
     anthraquinone derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Lee, Chang Hoon; Lee, Kee-Jung.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis,&amp;nbsp; (12), 1941-1946; 2004&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Palladium-catalyzed
     cross-coupling reaction of organobismuth compounds with aryl and alkenyl
     chlorides.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Yamazaki, Osamu; Tanaka, Toshifumi;
     Shimada, Shigeru; Suzuki, Yohichi; Tanaka, Masato. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synlett,&amp;nbsp; (11),
     1921-1924; 2004&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis, in vitro and in vivo
     activity of benzophenone-based inhibitors of steroid sulfatase.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;&lt;st1:place w:st=&quot;on&quot;&gt;Hejaz&lt;/st1:place&gt;,
     Hatem A. M.; Woo, L. W. Lawrence; Purohit, Atul; Reed, Michael J.; Potter,
     Barry V. L.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bioorganic &amp;amp; Medicinal Chemistry, 12(10), 2759-2772; 2004&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reaction of chloronaphthoquinones with
     phenylhydrazones as azaenamines in pyridine.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Berghot, M. A.; Badawy, D. S.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chemical
     Papers, 57(5), 342-349; 2003&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of N-quinonyltaurines.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Gorohovsky, S.; Temtsin-Krayz, G.;
     Bittner, S.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Amino Acids, 24(3),
     281-287; 2003 &lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;New access to the chemistry of
     piperonylidinyl-4-[2.2]-paracyclophanylamine and some electron &lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; -deficients.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;El-Shaieb, Kamal M.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal
     of the Chinese Chemical Society (&lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:city w:st=&quot;on&quot;&gt;Taipei&lt;/st1:city&gt;,
      &lt;st1:country-region w:st=&quot;on&quot;&gt;Taiwan&lt;/st1:country-region&gt;&lt;/st1:place&gt;),
     51(2), 321-325; 2004&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Phthalazinone in heterocyclic
     synthesis: Synthesis of some s-triazole, s-triazolothiadiazine,
     s-triazolothiadiazine, and s-triazolothiadiazole derivatives as
     pharmaceutical interest.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Abd El-Baset Hassanien, Abu Zeid.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.ingentaconnect.com/content/tandf/gpss/2003/00000178/00000009/art00014&quot;&gt;Phosphorus,&lt;/a&gt;
     Sulfur and Silicon and the Related Elements, 178(9), 1987-1997; 2003&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Novel Fused D-A
     Dyad and A-D-A Triad Incorporating Tetrathiafulvalene and p-Benzoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Dumur, Frederic; Gautier, Nicolas; Gallego-Planas,
     Nuria; Sahin, Yuecel; Levillain, Eric; Mercier, Nicolas; Hudhomme,
     Pietrick; Masino, Matteo; Girlando, Alberto; Lloveras, Vega;
     Vidal-Gancedo, Jose; Veciana, Jaume; Rovira, Concepcio. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Organic Chemistry, 69(6), 2164-2177; 2004&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Syntheses of hitherto unknown thiazole,
     ylidene and pyridinethione derivatives having a piperidin-1-yl moiety and
     their use as antimicrobial agents.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;El-Gaby, Mohamed Sayed A.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal
     of the Chinese Chemical Society (&lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:city w:st=&quot;on&quot;&gt;Taipei&lt;/st1:city&gt;,
      &lt;st1:country-region w:st=&quot;on&quot;&gt;Taiwan&lt;/st1:country-region&gt;&lt;/st1:place&gt;),
     51(1), 125-134; 2004&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Solid-phase synthesis of 2-amino-3-chloro-5- and
     8-nitro-1,4-naphthoquinones: a new and general colorimetric test for
     resin-bound amines.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Blackburn, Christopher. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron Letters, 46(9), 1405-1409; 2005 &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Process for preparation of naphthoquinonothiazole
     derivatives as organic third-order non-linear optical materials.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Gao, Jianrong; Sheng, Weijian; Xiang,
     Bin; Shan, Weiguang; Cheng, Lubai. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: red; font-size: 10pt; line-height: 150%;&quot;&gt;Faming Zhuanli Shenqing Gongkai Shuomingshu, 1440966, 10 Sep
     2003&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Process for
     preparation of bisnaphthotetrathiafulvalene derivatives as organic
     non-linear optical materials.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Gao, Jianrong; Shan, Weiguang; Xiang,
     Bin; Huang, Min; Cheng, Lubai. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Faming Zhuanli
     Shenqing Gongkai Shuomingshu, 1415612, 07 May 2003&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and
     biological activity of carnosine derivative of 1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;El Idrissi, A.; Zhurakhlvska, L. R.;
     Marintsova, N. H.; Taras, T. M.; Novikov, V. P.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Medichna
     Khimiya, 6(3), 139-140; 2004&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Studies on Charge-Transfer Complexes of
     2,3-Dicyano-1,4-naphthoquinone with Some Ring and N-Substituted Anilines.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Neelgund, Gururaj M.; Budni, M. L. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Monatshefte fuer Chemie, 135(11), 1395-1407; 2004 &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of
     natural carnosine derivative of 1,4-naphthoquinone and it&#39;s antihypoxic
     effect.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;El Idrissi, A.; Novikov, V. P. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Farmatsevtichnii Zhurnal (&lt;st1:city w:st=&quot;on&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;Kiev&lt;/st1:place&gt;&lt;/st1:city&gt;),&amp;nbsp; (2), 40-44; 2004&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;A stereoselective synthesis of
     spiro-dioxolanes via the multicomponent reaction of dicarbomethoxycarbene,
     aldehydes and 1,2- or 1,4-diones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Nair, Vijay; Mathai, Sindhu; Mathew,
     Smitha C.; Rath, Nigam P.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron, 61(11), 2849-2856; 2005&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;A
     direct one-pot synthesis of naphtho[2,3-b]furan-4,9-dione derivatives via
     C,O-dialkylation of &lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;
     -dicarbonyl compounds by 2,3-dichloro-1,4-naphthoquinones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Hu, Hua-You; Zhu, Ye; Wang, Lei; Xu,
     Jian-Hua. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis,&amp;nbsp; (10), 1605-1610; 2005&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Interaction of
     2,3-dichloro-1,4-naphthoquinone with n-butylamine in halocarbon solvents.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Neelgund, Gururaj M.; Budni, M. L. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Spectrochimica Acta, Part A: Molecular and Biomolecular
     Spectroscopy, 61A(8), 1729-1735; 2005&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Preparation of diamino quinone amides
     that modulate the levels of gene expression in cellular systems.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Padia, Janak K.; O&#39;Brien, Sean; Lu,
     Jiemin; Pikul, Stanislaw. &lt;/span&gt;&lt;st1:country-region w:st=&quot;on&quot;&gt;&lt;st1:place w:st=&quot;on&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;U.S.&lt;/span&gt;&lt;/st1:place&gt;&lt;/st1:country-region&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Pat. Appl. Publ., 2005032794, 10 Feb 2005&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Preparation of substituted quinone
     diamines that modulate levels of gene expression in cellular systems.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Padia, Janak K.; O&#39;Brien, Sean; Lu,
     Jiemin; Pikul, Stanislaw.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;PCT Int. Appl., 2005013903, 17 Feb 2005&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Base catalyzed synthesis of novel fused
     imidazoles from N-vinyl-1H-imidazole.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Aly, Ashraf A.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Zeitschrift
     fuer Naturforschung, B: Chemical Sciences, 60(1), 106-112; 2005&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Ligand Induced Stereoisomers Revealed
     in Copper(II) Complex of Nitrolawsone Oxime: EPR and Electronic Spectral
     Studies.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Rane, S.; Khan, E.; Khursheed, Ah.;
     Salunke-Gawali, S. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and Reactivity
     in Inorganic, Metal-Organic, and Nano-Metal Chemistry, 35(5), 343-353;
     2005&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Design, synthesis, and biological
     evaluation of novel naphthoquinone derivatives with CDC25 phosphatase
     inhibitory activity.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Brun, Marie-Priscille; Braud,
     Emmanuelle; Angotti, Delphine; Mondesert, Odile; Quaranta, Muriel; Montes,
     Matthieu; Miteva, Maria; Gresh, Nohad; Ducommun, Bernard; Garbay,
     Christiane. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bioorganic &amp;amp; Medicinal Chemistry,
     13(16), 4871-4879; 2005&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Sulfur-containing derivatives of 1,4-naphthoquinone.
     Part 1. Disulfide synthesis.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Stasevych, Maryna V.; Plotnikov, Maxym
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     Novikov, Volodymyr P. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Heteroatom Chemistry,
     16(3), 205-211; 2005&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis,
     acute toxicity, and antihypoxic and antiischemic activity of new amino
     acid derivatives of 1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Zhurakhivskaya, L. R.;
     Komarovskaya-Porokhnyavets, E. Z.; Marintsova, N. G.; Novikov, V. P.;
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     Makonchuk, D. Yu.; Lysun, V. M. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Farmatsevtichnii
     Zhurnal (Kiev, Ukraine),&amp;nbsp; (3),
     67-73; 2005&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Preparation of
     naphthoquinone derivatives as PI3 kinase inhibitors for treatment of
     cancer.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Chang, Junbiao; Xie, Weilin; Wang, Lei. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Faming Zhuanli Shenqing Gongkai Shuomingshu, 1587255, 02 Mar
     2005&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;A novel all-organic chemical and electrochemical
     fluorescent switch.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Illos, R. A.; Harlev, E.; Bittner,
     S.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron Letters, 46(48), 8427-8430; 2005&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of some new biologically
     active 1,2,4-triazoles, triazolothiadiazoles, triazolothaidiazines,
     triazolothiadiazepine bearing sulfonamide moiety.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Al-Sehemi, A. G. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chemistry (&lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:city w:st=&quot;on&quot;&gt;Rajkot&lt;/st1:city&gt;,
      &lt;st1:country-region w:st=&quot;on&quot;&gt;India&lt;/st1:country-region&gt;&lt;/st1:place&gt;),
     2(5), 139-145; 2005&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reaction of enamines of the
     1,2,3,4-tetrahydrobenzo[f]isoquinoline series with
     2,3-dichloro-1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Polygalova, N. N.; Mikhailovskii, A. G.;
     Gein, V. L.; Vakhrin, M. I.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Chemistry of Heterocyclic Compounds (&lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:city w:st=&quot;on&quot;&gt;New York&lt;/st1:city&gt;, &lt;st1:state w:st=&quot;on&quot;&gt;NY&lt;/st1:state&gt;, &lt;st1:country-region w:st=&quot;on&quot;&gt;United States&lt;/st1:country-region&gt;&lt;/st1:place&gt;), 41(2),
     258-259; 2005&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Simple Electrooptical Sensors for
     Inorganic Anions.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Anzenbacher, Pavel, Jr.; Palacios, Manuel
     A.; Jursikova, Karolina; Marquez, Manuel. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Organic
     Letters, 7(22), 5027-5030; 2005&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naphthofuroquinone derivatives: DNA
     topoisomerase-I inhibition and cytotoxicity.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Cho, Heeyeong; Park, Su-Jin; Lee,
     Kee-In. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bulletin
     of the Korean Chemical Society, 26(11), 1829-1832; 2005&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;A 24-Crown-8 Bearing Naphthalene and
     Naphthoquinone Chromophores.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Hogan, Conor F.; Hutchison, James A.;
     Ghiggino, Kenneth P.; Langford, Steven J.; Latter, Melissa J.; Lau,
     Vei-Lin; Murali, Venghatraghavan. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.informaworld.com/smpp/content~content=a727653889~db=all~order=page&quot;&gt;Supramolecular
     Chemistry, 17(7), 513-519; 2005&lt;/a&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of some new spiro
     naphtho[2,3-d][1,3]dithiole-4,9-dione derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;El-Shafie, A. K.; Soliman, A. M.;
     Sultan, A. A.; Abd-Alla, E. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;Journal of
     Heterocyclic Chemistry, 43(1), 133-137; 2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Preparation of
     2-hydroxy-3-(4-pyridyl)-1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Xu, Wei; Zou, Zhenguang; Lu, Yinxiang. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;Faming Zhuanli Shenqing Gongkai Shuomingshu, 1775757,
     24 May 2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Palladium-catalyzed amination of
     2,3-dichloro-1,4-naphthoquinone with nitroarylamines.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Wang, Xiao-Lei; Zheng, Xiu-Fang; Reiner,
     John.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synlett,&amp;nbsp; (6), 942-944; 2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Process for preparation of
     2,3-dichloro-1,4-naphthalenedione.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Xu, Guanghui.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Faming
     Zhuanli Shenqing Gongkai Shuomingshu, 1733678, 15 Feb 2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Regiocontrolled synthesis and HIV
     inhibitory activity of unsymmetrical binaphthoquinone and trimeric
     naphthoquinone derivatives of conocurvone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Stagliano, Kenneth W.; Emadi, Ashkan;
     Lu, Zhenhai; Malinakova, Helena C.; Twenter, Barry; Yu, Min; Holland,
     Louis E.; Rom, Amanda M.; Harwood, John S.; Amin, Ronak; Johnson, Allison
     A.; Pommier, Yves. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bioorganic &amp;amp;
     Medicinal Chemistry, 14(16), 5651-5665; 2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reductive heterocyclization of
     2,3-dichloro-1,4-naphthoquinone into
     naphtho[2,3-f][1,2,3,4,5]pentathiepine-6,11-diol under the action of
     sodium hydrosulfide in DMF.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Polonik, S. G.; Dmitrenok, P. S.;
     Makhan&#39;kov, V. V.; Anufriev, V. F.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Russian Journal of Organic Chemistry, 42(2), 302-303; 2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt left 114.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naphthofuroquinone
     derivatives: Inhibition of receptor tyrosine kinases.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Lee, Kee-In; Park, Youmie; Park, Su-Jin;
     Hwang, Jung-Hwan; Lee, Sung-Jin; Kim, Gun-Do; Park, Woo-Kyu; Lee, Sunghou;
     Jeong, Daeyoung; Kong, Jae-Yang; Kang, Hee-Kyoung; Cho, Heeyeong. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bioorganic &amp;amp; Medicinal Chemistry Letters, 16(3), 737-742;
     2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Charge-transfer interaction of
     4,13-diamino[2.2]paracyclophane with &lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; -acceptors.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;El-Shaieb, Kamal M.; Mourad,
     Aboul-Fetouh E.; Hopf, Henning.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://content.arkat-usa.org/ARKIVOC/JOURNAL_CONTENT/manuscripts/2006/06-1614FP%20as%20published%20mainmanuscript.pdf&quot;&gt;ARKIVOC
     (Gainesville, FL, United States),&amp;nbsp;
     (2), 193-200; 2006&lt;/a&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Design,
     synthesis, and biological evaluation of
     1,2,3-trisubstituted-1,4-dihydrobenzo[g]quinoxaline-5,10-diones and
     related compounds as antifungal and antibacterial agents.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Tandon, Vishnu K.; Yadav, Dharmendra B.;
     Maurya, Hardesh K.; Chaturvedi, Ashok K.; Shukla, Praveen K. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bioorganic &amp;amp; Medicinal Chemistry, 14(17), 6120-6126; 2006 &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;A convenient
     synthesis of 2-formyl-1,4,5,8-tetramethoxynaphthalene.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Xu, De-Feng; Guan, Peng-Jian; Li,
     Shao-Shun.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of Chemical Research,&amp;nbsp;
     (12), 779-780; 2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;i&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;α&lt;/span&gt;&lt;/i&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;-Vinylation
     of Haloquinones with Methyl Acrylate and MVK under Baylis-Hillman Reaction
     Conditions&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Lee, Seung Won; Lee, Chang Hoon; Lee, Kee-Jung&lt;b&gt; &lt;/b&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;Bulletin of the Korean
     Chemical Society, 27(5), 769-772; 2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;New cytotoxic
     furoquinones obtained from terpenyl-1,4-naphthoquinones and
     1,4-anthracenediones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Miguel del Corral, Jose M.; Castro, M.
     Angeles; Oliveira, Alaide B.; Gualberto, Simone A.; Cuevas, Carmen; San
     Feliciano, Arturo.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bioorganic &amp;amp; Medicinal Chemistry, 14(21), 7231-7240; 2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of benzo[f]indole-4,9-dione
     and benzo[b]carbazole-6,11-dione derivatives via one-pot sequential
     C,N-dialkylation of enaminones of &lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; -diketones and ketoesters by
     2,3-dichloronaphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Hu, Hua-You; Liu, Yun; Ye, Miao; Xu,
     Jian-Hua. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synlett,&amp;nbsp; (12), 1913-1917; 2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Study on synthesis of
     2,3-dichloro-1,4-naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Cao, Xiao-qun; Liu, Xin; Cheng,
     Yue-shan.&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Jingxi
     Yu Zhuanyong Huaxuepin, 14(3/4), 16-17; 2006 &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Quinone-Annulated N-Heterocyclic
     Carbene-Transition-Metal Complexes: Observation of &lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; -Backbonding Using FT-IR
     Spectroscopy and Cyclic Voltammetry.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Sanderson, Matthew D.; Kamplain, Justin
     W.; Bielawski, Christopher W.&amp;nbsp;&amp;nbsp;&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Journal of the American Chemical Society, 128(51), 16514-16515;
     2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;N-aryl-and N-vinyldiaza-18-crown-6:
     Synthesis and complexing ability.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Sazonov, P. K.; Artamkina, G. A.;
     Beletskaya, I. P. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Russian Journal of
     Organic Chemistry, 42(3), 438-447; 2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Process for
     preparation of naphtho[2,3-e][1,4,2]oxazaphosphinane derivatives for
     treatment of tumor.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Chen, Ruyu; Wang, Bin.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Faming
     Zhuanli Shenqing Gongkai Shuomingshu, 1858056, 08 Nov 2006 &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Process for preparation of benzonaphthodithiino-thianthrene-hexone
     as third-order nonlinear organic optical material.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Gao, Jianrong; Cai, Zhibin; Sheng,
     Weijian; Jia, Jianhong; Xiang, Bin. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;Faming Zhuanli Shenqing Gongkai Shuomingshu, 1884282, 27 Dec
     2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Naphtho[2,3-b][1,4]-thiazine-5,10-diones
     and 3-substituted-1,4-dioxo-1,4-dihydronaphthalen-2-yl-thioalkanoate
     derivatives: Synthesis and biological evaluation as potential
     antibacterial and antifungal agents.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Tandon, Vishnu K.; Maurya, Hardesh K.;
     Yadav, Dharmendra B.; Tripathi, Ashutosh; Kumar, Manish; Shukla, Praveen
     K. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bioorganic &amp;amp; Medicinal Chemistry
     Letters, 16(22), 5883-5887; 2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Collection of Czechoslovak Chemical Communications, 71(1),
     59-76; 2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; margin-right: -36.0pt; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Reaction
     products of arylethenyl benzofuranyl ketones and their antimicrobial
     activity.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Micky, J. A. A.; Saleh, N. M.; Mohamed,
     S. M.; Mohamed, S. A.; Salem, M. M.&amp;nbsp;&amp;nbsp;&amp;nbsp;
     &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Indian Journal of Chemistry, Section B:
     Organic Chemistry Including Medicinal Chemistry, 45B(6), 1579-1583; 2006&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis, cytotoxicity, and DNA topoisomerase II
     inhibitory activity of benzofuroquinolinediones.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Rhee, Hee-Kyung; Park, Hyen Joo; Lee,
     Sang Kook; Lee, Chong-Ock; Choo, &lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:placename w:st=&quot;on&quot;&gt;Hea-Young&lt;/st1:placename&gt; &lt;st1:placetype w:st=&quot;on&quot;&gt;Park&lt;/st1:placetype&gt;&lt;/st1:place&gt;.
     &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;Bioorganic &amp;amp; Medicinal
     Chemistry, 15(4), 1651-1658; 2007&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of polycyclic indolizine derivatives via
     one-pot tandem reactions of N-ylides with dichloro substituted&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;-unsaturated
     carbonyl compounds.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Liu, Yun; Hu, Hua-You; Liu, Qing-Jian;
     Hu, Hong-Wen; Xu, Jian-Hua. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;Tetrahedron,
     63(9), 2024-2033; 2007&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis of eight-, nine-, and
     ten-membered, nitrogen-containing quinone-fused heterocycles.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Yerushalmi, Sarit; Lemcoff, N. Gabriel;
     Bittner, Shmuel&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;span style=&quot;color: blue;&quot;&gt;Synthesis, (2),
     239-242; 2007&lt;/span&gt;.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Quinone
     antitumor compounds, particularly 1,4-anthraquinones and their
     derivatives, process for their preparation, and their uses.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp; &lt;b&gt;&amp;nbsp;&amp;nbsp;&lt;/b&gt;&amp;nbsp;&amp;nbsp;Molina Orden, Maria Teresa; Honghao,
     Sun; Taliansky Chamudis, Sandra; Carnero Moya, Amancio; Blanco Rodriguez,
     Fernando; Moneo Ocana, Maria Victoria. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;PCT
     Int. Appl., 2007026041, 08 Mar 2007 ( Cl and Br)&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Synthesis and &lt;i&gt;In
     Vitro&lt;/i&gt; Cytotoxicity Evaluation of Novel Naphthindolizinedione
     Derivatives.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Defant, Andrea; Guella, Graziano; Mancini,
     Ines &amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Archiv der Pharmazie (&lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:city w:st=&quot;on&quot;&gt;Weinheim&lt;/st1:city&gt;, &lt;st1:country-region w:st=&quot;on&quot;&gt;Germany&lt;/st1:country-region&gt;&lt;/st1:place&gt;), 340(3), 147-153;
     2007&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.sciencedirect.com/science?_ob=ArticleURL&amp;amp;_udi=B6TF8-4NNYJ67-4&amp;amp;_user=10&amp;amp;_coverDate=08%2F01%2F2007&amp;amp;_alid=1065864023&amp;amp;_rdoc=1&amp;amp;_fmt=high&amp;amp;_orig=search&amp;amp;_cdi=5220&amp;amp;_sort=r&amp;amp;_docanchor=&amp;amp;view=c&amp;amp;_ct=2&amp;amp;_acct=C000050221&amp;amp;_version=1&amp;amp;_urlVersion=0&amp;amp;_userid=10&amp;amp;md5=d4b69fff81ac1b4a0fd18c547a21405b&quot;&gt;&lt;b&gt;The
     1,4-naphthoquinone scaffold in the design of cysteine protease inhibitors&lt;/b&gt;&lt;/a&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;.&amp;nbsp; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Valente, Cláudia;
     Moreira, Rui; Guedes, Rita C.; Iley, Jim; Jaffar, Mohammed; Douglas&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Kenneth
     T. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Bioorganic
     &amp;amp; Medicinal Chemistry, 15(15), 5340-5350; 2007&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;
     &lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.informaworld.com/smpp/content~db=all~content=a771126652&quot; title=&quot;Click to view this record&quot;&gt;Rhodanine in Fused-Heterocycles
     Syntheses&lt;/a&gt;. &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Mourad;&amp;nbsp; Aboul-Fetouh E.; Hassan;&amp;nbsp;
     Alaa A.; Aly, Ashraf A.;&amp;nbsp; Mohamed, Nasr K.; Ali,&lt;b&gt; &lt;/b&gt;Bahaa A. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Phosphorus, Sulfur
     and Silicon and the Related Elements, 182(2), 321-331; 2007&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Benzo-
     and naphthoimidazoxadiazolediene, naphthobisthiazole as well as
     naphthothiazine derivatives from 1-acylthiosemicarbazides.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;
     Hassan, Alaa A.; Mourad, Aboul Fetouh E.; Zied, Ashraf H. Abou&lt;i&gt; &lt;/i&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;ARKIVOC (&lt;st1:place w:st=&quot;on&quot;&gt;&lt;st1:city w:st=&quot;on&quot;&gt;Gainesville&lt;/st1:city&gt;, &lt;st1:state w:st=&quot;on&quot;&gt;FL&lt;/st1:state&gt;,
      &lt;st1:country-region w:st=&quot;on&quot;&gt;United States&lt;/st1:country-region&gt;&lt;/st1:place&gt;),&amp;nbsp; (1), 222-235; 2007&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;span lang=&quot;EN-US&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;3-Benzoyl-1,2-diphenyl-1&lt;span class=&quot;it&quot;&gt;&lt;i&gt;H&lt;/i&gt;&lt;/span&gt;-benz[&lt;span class=&quot;it&quot;&gt;&lt;i&gt;f&lt;/i&gt;&lt;/span&gt;]indole-4,9-dione.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;a href=&quot;http://scripts.iucr.org/cgi-bin/citedin?search_on=name&amp;amp;author_name=Liu,%20Y.&quot;&gt;&amp;nbsp;Liu&lt;/a&gt;, Y.; &lt;a href=&quot;http://scripts.iucr.org/cgi-bin/citedin?search_on=name&amp;amp;author_name=Lu,%20Z.-F.&quot;&gt;&amp;nbsp;Lu&lt;/a&gt;, Z.-F.; &lt;a href=&quot;http://scripts.iucr.org/cgi-bin/citedin?search_on=name&amp;amp;author_name=Ye,%20M.&quot;&gt;&amp;nbsp;Ye&lt;/a&gt;, M.; &lt;a href=&quot;http://scripts.iucr.org/cgi-bin/citedin?search_on=name&amp;amp;author_name=Zhang,%20Y.&quot;&gt;&amp;nbsp;Zhang&lt;/a&gt;,&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Y.; &lt;a href=&quot;http://scripts.iucr.org/cgi-bin/citedin?search_on=name&amp;amp;author_name=Xu,%20J.-H.&quot;&gt;&amp;nbsp;Xu&lt;/a&gt;;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;J.-H.&lt;/span&gt;&lt;span lang=&quot;EN-US&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;Acta
     Crystallographica, Section E: Structure Reports Online, E63(5),
     o2066-o2067; 2007&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;A simple and
     convenient procedure for the synthesis of naphthoquinone fused cyclic alpha&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;b&gt;-aminophosphoryl
     chloride.&amp;nbsp;&lt;/b&gt;&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Wang, Bin; Miao, Zhiwei; Chen,&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Ruyu&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Heteroatom
     Chemistry, 18(4), 359-362; 2007&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;3&lt;b&gt;-Acetyl-1-(4-chlorophenyl)-2-methylbenzo[&lt;span class=&quot;it&quot;&gt;&lt;i&gt;f&lt;/i&gt;&lt;/span&gt;]indole-4,9-dione&lt;/b&gt;. &lt;a href=&quot;http://scripts.iucr.org/cgi-bin/citedin?search_on=name&amp;amp;author_name=Fun,%20H.-K.&quot;&gt;&amp;nbsp;Fun&lt;/a&gt;, H.-K.; &lt;a href=&quot;http://scripts.iucr.org/cgi-bin/citedin?search_on=name&amp;amp;author_name=Chantrapromma,%20S.&quot;&gt;Chantrapromma&lt;/a&gt;,
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&lt;li class=&quot;MsoNormal&quot; style=&quot;color: blue; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;a href=&quot;http://www.informaworld.com/smpp/content~db=all~content=a775706621&quot; title=&quot;Click to view this record&quot;&gt;2-Aminothiophenol as building blocks for
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     Chemistry, 28(2), 223-229; 2007&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;color: red; line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt; text-align: justify;&quot;&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Hecheng Huaxue, 15(1), 16-19;
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     from 1,4-naphthoquinons&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;. Tandon, Vishnu K.; Maurya, Hardesh K&lt;span style=&quot;color: blue;&quot;&gt;.&amp;nbsp; Heterocycles
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&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;Facile and
     Efficient Synthesis of Novel Oxazine, Oxazepine and Phenoxazine of
     Chromenones Fused with 1,4-Naphthoquinone.&lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; Tandon, Vishnu K.; Maurya,
     Hardesh K. &lt;span style=&quot;color: blue;&quot;&gt;&amp;nbsp;Heterocycles 77(1), 611-615; 2009&lt;/span&gt;&lt;b&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/b&gt;&lt;/span&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;2,3-Disubstituted-1,4-naphthoquinones,
     12H-benzo[b]phenothiazine-6,11-diones andrelated compounds:&amp;nbsp; Synthesis and Biological evaluation as
     potential antiproliferative and antifungal agents. &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tandon, Vishnu K.;
     Maurya, Hardesh K.; &lt;span style=&quot;color: blue;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tripathi, Ashutosh; ShivaKeshava, G.B.;&amp;nbsp; Shukla, Praveen &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;K&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;.;
     Srivastava, Pallavi; Panda&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Dulal&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt; &amp;nbsp;&amp;nbsp;&lt;span style=&quot;color: blue;&quot;&gt;European
     Journal of Medicinal Chemistry 44(3), 1086-1092; 2009.&lt;/span&gt;&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/b&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Design, synthesis and biological evaluation of novel nitrogen and
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     antibacterial agents. &lt;/span&gt;&lt;/b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Tandon, Vishnu K.; Maurya, Hardesh K.; &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;Mishra, Nripendra N.; Shukla, Praveen &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;K&lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;. &lt;/span&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;color: blue; font-size: 10pt; line-height: 150%;&quot;&gt;European Journal of Medicinal Chemistry 44(8), 3130-3137;
     2009.&lt;/span&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&lt;o:p&gt;&lt;/o:p&gt;&lt;/span&gt;&lt;/b&gt;&lt;/li&gt;
&lt;li class=&quot;MsoNormal&quot; style=&quot;line-height: 150%; mso-list: l13 level1 lfo3; tab-stops: list 36.0pt;&quot;&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/b&gt;&lt;b&gt;&lt;span lang=&quot;EN-US&quot; style=&quot;font-size: 10pt; line-height: 150%;&quot;&gt;‘On water’: unprecedented nucleophilic
     substitution and addition reactions with 1,4-quinones in aqueous
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     Letters 50, 5896-5902; 2009.&lt;/span&gt;&lt;/span&gt;&lt;/li&gt;
&lt;/ol&gt;
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&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://naphthoquinone.blogspot.com/feeds/4944739417997742979/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='http://naphthoquinone.blogspot.com/2011/09/structure-synonyms-and-basic.html#comment-form' title='1 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/7775904593195892177/posts/default/4944739417997742979'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/7775904593195892177/posts/default/4944739417997742979'/><link rel='alternate' type='text/html' href='http://naphthoquinone.blogspot.com/2011/09/structure-synonyms-and-basic.html' title='2,3-Dichloro-1,4-naphthoquinone'/><author><name>Hardesh</name><uri>http://www.blogger.com/profile/15195689814375098224</uri><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='https://img1.blogblog.com/img/b16-rounded.gif'/></author><media:thumbnail xmlns:media="http://search.yahoo.com/mrss/" url="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEjbtKkGuQ04FpMetfcxbMqzePVR784PLwsXfD2bAlzTpn3oo0ViZPju3IrLmCUyIaOHI_R39xbYqdudTQyJidJ5qzmcKO0RzyepBF5fd8mETVszz6ue6iERexgYhAIRzb7E5OnXWeh3xdM/s72-c/d.bmp" height="72" width="72"/><thr:total>1</thr:total></entry></feed>