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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22258" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/22258</id>
  <updated>2026-10-16T02:12:21Z</updated>
  <dc:date>2026-10-16T02:12:21Z</dc:date>
  <entry>
    <title>Neo coramandaline, a pyrrolizidine alkaloid from &lt;i&gt;Cynoglossum furcatum&lt;/i&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22470" />
    <author>
      <name>Ravi, S</name>
    </author>
    <author>
      <name>Lakshmanan, A J</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22470</id>
    <updated>2013-10-25T16:40:48Z</updated>
    <published>2000-01-01T00:00:00Z</published>
    <summary type="text">Title: Neo coramandaline, a pyrrolizidine alkaloid from &lt;i&gt;Cynoglossum furcatum&lt;/i&gt;
Authors: Ravi, S; Lakshmanan, A J
Abstract: The pyrrolizidine alkaloids of &lt;i&gt;Cynoglossum&#xD;
furcatum &lt;/i&gt;have been isolated and characterised. They are neo&#xD;
coramandaline &lt;b&gt;1&lt;/b&gt;, a new pyrrolizidine ester alkaloid and echinatine&#xD;
&lt;b&gt;3&lt;/b&gt;. Neo&#xD;
&#xD;
coramandaline is formulated as 9-O-(-)viridifloryl&#xD;
laburnine on the basis of spectroscopic measurements and hydrolysis.
Page(s): 80-82</summary>
    <dc:date>2000-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis of new substituted sulfonylhydrazinecarboxamides and sulfonylhydrazine carbothioamides having antifungal and antibacterial activities</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22469" />
    <author>
      <name>Nalavde, Yogesh Madhukar</name>
    </author>
    <author>
      <name>Joshi, Vidya</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22469</id>
    <updated>2013-10-23T16:38:10Z</updated>
    <published>2000-01-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis of new substituted sulfonylhydrazinecarboxamides and sulfonylhydrazine carbothioamides having antifungal and antibacterial activities
Authors: Nalavde, Yogesh Madhukar; Joshi, Vidya
Abstract: &lt;i&gt;p&lt;/i&gt;-Toluenesulfonylhydrazide&#xD;
&lt;b&gt;3&lt;/b&gt; on condensation with substituted phenyl isocyanates &lt;b&gt;2a-i&lt;/b&gt; and substituted&#xD;
phenyl isothiocyanates &lt;b&gt;2j-p&lt;/b&gt; gives &lt;i&gt;N&lt;/i&gt;,2-disubstituted sulfonylhydrazinecarboxamides&#xD;
&lt;b&gt;4a-i&lt;/b&gt; and &lt;i&gt;N, &lt;/i&gt;2-disubstituted sulfonylhydrazinecarbothioamides &lt;b&gt;4j-p&lt;/b&gt;&#xD;
respectively. Compounds &lt;b&gt;4a-p&lt;/b&gt; have been found to be bactericidal against &lt;i&gt;S.&#xD;
aureus &lt;/i&gt;and &lt;i&gt;S. typhi &lt;/i&gt;while compound &lt;b&gt;4n&lt;/b&gt; shows fungicidal activity&#xD;
against &lt;i&gt;T. mentagrophytes &lt;/i&gt;and &lt;i&gt;T.rubrum.&lt;/i&gt;
Page(s): 76-79</summary>
    <dc:date>2000-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Oxidative transformation of alcohols and oximes to carbonyl compounds by quinolinium fluorochromate (QFC)</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22468" />
    <author>
      <name>Rajkumar, G Abraham</name>
    </author>
    <author>
      <name>Arabindoo, Banumathi</name>
    </author>
    <author>
      <name>Murugesan, V</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22468</id>
    <updated>2013-10-22T16:41:40Z</updated>
    <published>2000-01-01T00:00:00Z</published>
    <summary type="text">Title: Oxidative transformation of alcohols and oximes to carbonyl compounds by quinolinium fluorochromate (QFC)
Authors: Rajkumar, G Abraham; Arabindoo, Banumathi; Murugesan, V
Abstract: Oxidation of selected alcohols and oximes&#xD;
to the corresponding carbonyl compounds has been achieved with quinolinium fluorochromate&#xD;
(QFC) in dichloromethane solvent under reflux conditions. The oxidation&#xD;
reactions have been found to be smooth and gave the products in good yield.
Page(s): 74-75</summary>
    <dc:date>2000-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Liquid phase oxidation of saturated nitrogen-containing heterocyclics over modified MCM-41 molecular sieves&lt;sup&gt;+&lt;/sup&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/22467" />
    <author>
      <name>Chandrakala, M</name>
    </author>
    <author>
      <name>Murthy, K V V S B S R</name>
    </author>
    <author>
      <name>Kulkarni, S J</name>
    </author>
    <author>
      <name>Raghavan, K V</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/22467</id>
    <updated>2013-10-22T16:41:35Z</updated>
    <published>2000-01-01T00:00:00Z</published>
    <summary type="text">Title: Liquid phase oxidation of saturated nitrogen-containing heterocyclics over modified MCM-41 molecular sieves&lt;sup&gt;+&lt;/sup&gt;
Authors: Chandrakala, M; Murthy, K V V S B S R; Kulkarni, S J; Raghavan, K V
Abstract: For the first&#xD;
time, the liquid&#xD;
phase oxidation reactions of saturated N-heterocyclics like piperidine and pyrrolidine&#xD;
to piperidone and pyrrolidone have been carried out over modified MCM-41 molecular&#xD;
sieves with 30-55% yield and &gt;80% selectivity.
Page(s): 71-73</summary>
    <dc:date>2000-01-01T00:00:00Z</dc:date>
  </entry>
</feed>

