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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/15882</link>
    <description />
    <pubDate>Sat, 10 Oct 2026 22:34:32 GMT</pubDate>
    <dc:date>2026-10-10T22:34:32Z</dc:date>
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      <title>Efficient and selective deprotection of aryl aldehyde diacetates catalyzed by tin(II) chloride dihydrate</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/16644</link>
      <description>Title: Efficient and selective deprotection of aryl aldehyde diacetates catalyzed by tin(II) chloride dihydrate
Authors: Baltork, I Mohammadpoor-; Aliyan, H
Abstract: A mild,efficient&#xD;
and excellent yield method for the selective deprotection of&#xD;
aryl aldehyde diacetates in the presence&#xD;
of &lt;sup&gt;.&lt;/sup&gt;phenolic acetate and aliphatic aldehyde diacetate using catalytic&#xD;
amounts of tin(II) chloride dihydrate (SnCl&lt;sub&gt;2&lt;/sub&gt;.2H&lt;sub&gt;2&lt;/sub&gt;O) is&#xD;
described.
Page(s): 1223-1225</description>
      <pubDate>Fri, 01 Oct 1999 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/16644</guid>
      <dc:date>1999-10-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>A facile and convenient method for the preparation of 2-styrylbenzimidazoles</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/16643</link>
      <description>Title: A facile and convenient method for the preparation of 2-styrylbenzimidazoles
Authors: Dubey, P K; Kumar, Ramesh; Grossert, J S; Hooper, D L
Abstract: Condensation of&#xD;
&lt;i&gt;o-&lt;/i&gt;phenylenediamine dihydrochloride with cinnamic&#xD;
acids in refluxing ethylene glycol yields the corresponding 2-styrylbenzimidazoles&#xD;
in excellent yields.
Page(s): 1211-1213</description>
      <pubDate>Fri, 01 Oct 1999 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/16643</guid>
      <dc:date>1999-10-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Ladderane-like motifs: Solid state architecture of trans-1,2-diphenyl-lcyclobutene-3,4-diol dinitrate</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/16642</link>
      <description>Title: Ladderane-like motifs: Solid state architecture of trans-1,2-diphenyl-lcyclobutene-3,4-diol dinitrate
Authors: Mehta, Goverdhan; Uma, R
Abstract: C&lt;sub&gt;2&lt;/sub&gt;Symmetric&#xD;
trans-1,2-diphenyl-l-cyclobutene-3,4-diol dinitrate&#xD;
defines a novel ladderane-Iike motif in the solid&#xD;
state&#xD;
&#xD;
through a network of C-H...O interactions between aromatic C-H donor and a weak acceptor like the nitrate ester group.
Page(s): 1154-1158</description>
      <pubDate>Fri, 01 Oct 1999 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/16642</guid>
      <dc:date>1999-10-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Chemical composition of the essential oil of &lt;i&gt;Artabotrys &lt;/i&gt;&lt;i&gt;odoratissimus&lt;/i&gt;</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/16641</link>
      <description>Title: Chemical composition of the essential oil of &lt;i&gt;Artabotrys &lt;/i&gt;&lt;i&gt;odoratissimus&lt;/i&gt;
Authors: Garg, S C; Siddiqui, Nafeesa
Abstract: The essential oil&#xD;
(0.24%) from the leaves of &lt;i&gt;Artabotrys odoratissimus &lt;/i&gt;R.Br. has&#xD;
been analysed by chromatographic, spectroscopic&#xD;
and chemical methods. Fifteen constituents&#xD;
(96.13%) have been characterised. The oil has&#xD;
been found rich in terpinen-4-ol (38.63%),&#xD;
caryophyllene oxide (11.78%) and linalool (11.17%).&lt;i&gt;&lt;/i&gt;
Page(s): 1229-1230</description>
      <pubDate>Fri, 01 Oct 1999 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/16641</guid>
      <dc:date>1999-10-01T00:00:00Z</dc:date>
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