<?xml version="1.0" encoding="UTF-8"?>
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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/15882" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/15882</id>
  <updated>2026-10-11T04:41:50Z</updated>
  <dc:date>2026-10-11T04:41:50Z</dc:date>
  <entry>
    <title>Efficient and selective deprotection of aryl aldehyde diacetates catalyzed by tin(II) chloride dihydrate</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/16644" />
    <author>
      <name>Baltork, I Mohammadpoor-</name>
    </author>
    <author>
      <name>Aliyan, H</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/16644</id>
    <updated>2016-07-20T05:47:26Z</updated>
    <published>1999-10-01T00:00:00Z</published>
    <summary type="text">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</summary>
    <dc:date>1999-10-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>A facile and convenient method for the preparation of 2-styrylbenzimidazoles</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/16643" />
    <author>
      <name>Dubey, P K</name>
    </author>
    <author>
      <name>Kumar, Ramesh</name>
    </author>
    <author>
      <name>Grossert, J S</name>
    </author>
    <author>
      <name>Hooper, D L</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/16643</id>
    <updated>2016-07-20T05:52:50Z</updated>
    <published>1999-10-01T00:00:00Z</published>
    <summary type="text">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</summary>
    <dc:date>1999-10-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Ladderane-like motifs: Solid state architecture of trans-1,2-diphenyl-lcyclobutene-3,4-diol dinitrate</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/16642" />
    <author>
      <name>Mehta, Goverdhan</name>
    </author>
    <author>
      <name>Uma, R</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/16642</id>
    <updated>2016-07-20T05:12:11Z</updated>
    <published>1999-10-01T00:00:00Z</published>
    <summary type="text">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</summary>
    <dc:date>1999-10-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Chemical composition of the essential oil of &lt;i&gt;Artabotrys &lt;/i&gt;&lt;i&gt;odoratissimus&lt;/i&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/16641" />
    <author>
      <name>Garg, S C</name>
    </author>
    <author>
      <name>Siddiqui, Nafeesa</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/16641</id>
    <updated>2016-07-20T06:03:39Z</updated>
    <published>1999-10-01T00:00:00Z</published>
    <summary type="text">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</summary>
    <dc:date>1999-10-01T00:00:00Z</dc:date>
  </entry>
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