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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22259" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/22259</id>
  <updated>2026-10-09T09:57:44Z</updated>
  <dc:date>2026-10-09T09:57:44Z</dc:date>
  <entry>
    <title>A new lipid glycoside from two &lt;i&gt;sinularia &lt;/i&gt;species of Andaman and Nicobar Islands&lt;sup&gt;†&lt;/sup&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22579" />
    <author>
      <name>Anjaneyulu, V</name>
    </author>
    <author>
      <name>Rao, P V Subba</name>
    </author>
    <author>
      <name>Radhika, P</name>
    </author>
    <author>
      <name>Laatsch, H</name>
    </author>
    <author>
      <name>Misra, L N</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22579</id>
    <updated>2013-10-26T16:43:04Z</updated>
    <published>2000-02-01T00:00:00Z</published>
    <summary type="text">Title: A new lipid glycoside from two &lt;i&gt;sinularia &lt;/i&gt;species of Andaman and Nicobar Islands&lt;sup&gt;†&lt;/sup&gt;
Authors: Anjaneyulu, V; Rao, P V Subba; Radhika, P; Laatsch, H; Misra, L N
Abstract: The more polar fractions of ethyl acetate&#xD;
solubles of &lt;i&gt;Sinularia gravis &lt;/i&gt;and &lt;i&gt;Sinularia &lt;/i&gt;species yield a new glycolipid&#xD;
and its structure has been deduced as 2-hydroxy-3-(octadecyloxy)-propyl-α-&lt;img src='http://www.niscair.res.in/jinfo/smaller.gif' border=0&gt;-fucopyranoside &lt;b&gt;1&lt;/b&gt;&#xD;
from its high resolution spectral data.
Page(s): 121-124</summary>
    <dc:date>2000-02-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Two new compounds from &lt;i&gt;Ligularia duciformis&lt;/i&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22502" />
    <author>
      <name>Gao, Kun</name>
    </author>
    <author>
      <name>Jia, Zhong-Jian</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22502</id>
    <updated>2013-10-23T16:42:36Z</updated>
    <published>2000-02-01T00:00:00Z</published>
    <summary type="text">Title: Two new compounds from &lt;i&gt;Ligularia duciformis&lt;/i&gt;
Authors: Gao, Kun; Jia, Zhong-Jian
Abstract: Two new compounds have been isolated from&#xD;
the roots of &lt;i&gt;Ligularia ducifonnis. &lt;/i&gt;Their structures have been established&#xD;
by spectroscopic studies and by comparison with closely related compounds.
Page(s): 160-161</summary>
    <dc:date>2000-02-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Studies on fused β-lactams: Synthesis, stereochemistry and antimicrobial activity of some new cepham analogues</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22501" />
    <author>
      <name>Sharma, S D</name>
    </author>
    <author>
      <name>Saluja, Aarti</name>
    </author>
    <author>
      <name>Bhaduri, Susmita</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22501</id>
    <updated>2013-10-26T16:43:38Z</updated>
    <published>2000-02-01T00:00:00Z</published>
    <summary type="text">Title: Studies on fused β-lactams: Synthesis, stereochemistry and antimicrobial activity of some new cepham analogues
Authors: Sharma, S D; Saluja, Aarti; Bhaduri, Susmita
Abstract: β-Lactam&#xD;
ring has been&#xD;
conveniently grafted onto 2-phenyl-5,6-dihydro-1,3 -thiazine &lt;b&gt;1&lt;/b&gt; by annelating&#xD;
it with &lt;i&gt;in situ &lt;/i&gt;prepared ketenes to furnish cepham analogues &lt;b&gt;6-9&lt;/b&gt;.&#xD;
A variety of acids such as menthoxy acetic acid &lt;b&gt;2&lt;/b&gt;, butylthioacetic acid &lt;b&gt;3&lt;/b&gt;,&#xD;
chloroacetic acid &lt;b&gt;4&lt;/b&gt; and benzotriazole acetic acid &lt;b&gt;5&lt;/b&gt; have been&#xD;
used as mixed sulphonic acid anhydrides for the cycloaddition reaction. All the&#xD;
compounds have been screened for their antibacterial activities.
Page(s): 156-159</summary>
    <dc:date>2000-02-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Oxazoles : Perturbations by methyl groups</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22500" />
    <author>
      <name>Rao, B Rajeshwar</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22500</id>
    <updated>2013-10-27T16:42:20Z</updated>
    <published>2000-02-01T00:00:00Z</published>
    <summary type="text">Title: Oxazoles : Perturbations by methyl groups
Authors: Rao, B Rajeshwar
Abstract: The effect of methyl groups in oxazoles&#xD;
has been studied and the perturbations caused on the oxygen and nitrogen atoms have&#xD;
been rationalized. The Hucke! Molecular Orbital (HMO) method has been used to evaluate&#xD;
the π-electron densities of all the molecules studied.
Page(s): 154-155</summary>
    <dc:date>2000-02-01T00:00:00Z</dc:date>
  </entry>
</feed>

