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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22266</link>
    <description />
    <items>
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        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/22578" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/22577" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/22576" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/22575" />
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    <dc:date>2026-10-10T21:42:57Z</dc:date>
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  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/22578">
    <title>Phytochemical investigation of &lt;i&gt;Tephrosia purpurea &lt;/i&gt;seeds</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22578</link>
    <description>Title: Phytochemical investigation of &lt;i&gt;Tephrosia purpurea &lt;/i&gt;seeds
Authors: Bhatnagar, Ramesh; Kapoor, R C
Abstract: Acetyl fraxinol and two new isoflavones&#xD;
7-&lt;i&gt;O&lt;/i&gt;-acetyl-8-methyl-2'-methoxy-isoflavone and 2' ,7-dimethoxy-8-methylisoflavone&#xD;
have been isolated from the seeds of &lt;i&gt;Tephrosia purpurea &lt;/i&gt;and characterised&#xD;
on the basis of spectral data analysis and chemical reactions.
Page(s): 879-882</description>
    <dc:date>2000-11-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/22577">
    <title>Triterpenoids from &lt;i&gt;Mosla chinensis&lt;/i&gt;</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22577</link>
    <description>Title: Triterpenoids from &lt;i&gt;Mosla chinensis&lt;/i&gt;
Authors: Zheng, Shangzhen; Kang, Shuhe; Shen, Tong; Sun, Liping; Shen, Xuwei
Abstract: Two new triterpenes,namely 3,25-epoxy-2β , 3α,7β-trihydroxyolean-12-en-28-oic acid and 3β-angeloyl-2β,23-dihydroxylean-12-en-28-oic acid, along with four&#xD;
known triterpenoids have been isolated from &lt;i&gt;Mosla chinensis.&#xD;
&lt;/i&gt;Their structures have been elucidated by means of&#xD;
spectral and chemical evidence.
Page(s): 875-878</description>
    <dc:date>2000-11-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/22576">
    <title>Two new aliphatic compounds from the leaves of &lt;i&gt;Ziziphus mauritiana&lt;/i&gt;</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22576</link>
    <description>Title: Two new aliphatic compounds from the leaves of &lt;i&gt;Ziziphus mauritiana&lt;/i&gt;
Authors: Agarwal, Santosh K; Singh, Sudhir S; Verma, Sushma; Kumar, Sushil
Abstract: Chemical investigation of the leaves of &lt;i&gt;Ziziphus&#xD;
mauritiana &lt;/i&gt;yields two new compounds characterised as&#xD;
decyl-8-hydroxyheptadecanoate&lt;i&gt; &lt;/i&gt;&lt;b&gt;1 &lt;/b&gt;and&#xD;
12-hydroxy-tetratriacontan-9-one &lt;b&gt;2&lt;/b&gt; using&lt;i&gt; &lt;/i&gt;IR, &lt;sup&gt;1&lt;/sup&gt;H NMR&#xD;
and mass spectral data.
Page(s): 872-874</description>
    <dc:date>2000-11-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/22575">
    <title>A facile phase-transfer catalysed N-methylation of 2-substituted benzimidazoles</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/22575</link>
    <description>Title: A facile phase-transfer catalysed N-methylation of 2-substituted benzimidazoles
Authors: Dubey, P K; Ramanatham, J; Kumar, Ramesh; Grossert, J S; Hooper, D L
Abstract: N-Alkyl-2-acetylbenzimidazoles have been&#xD;
obtained by alkylating 2-acetylbenzimidazole in CH&lt;sub&gt;3&lt;/sub&gt;CN at RT for 30&#xD;
min in over 90% yield using triethylbenzylammonium chloride as phasetransfer&#xD;
catalyst and anhyd. K&lt;sub&gt;2&lt;/sub&gt;CO&lt;sub&gt;3&lt;/sub&gt; as base. When the same conditions&#xD;
are used to methylate simple 2-alkylbenzimidazoles, poorer results were&#xD;
obtained. Optimum conditions have been worked out for the methylation of simple&#xD;
2-alkylbenzimidazoles by changing (a) the solvent, (b) the phase-transfer&#xD;
catalyst, (c) the concentration of the phase-transfer catalyst and (d) the type&#xD;
of phase-transfer catalysis itself. Using the optimised conditions, a number of&#xD;
l-methyl-2-alkylbenzimidazoles have been synthesised in a facile manner.
Page(s): 867-871</description>
    <dc:date>2000-11-01T00:00:00Z</dc:date>
  </item>
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