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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/6422" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/6422</id>
  <updated>2026-10-09T18:05:46Z</updated>
  <dc:date>2026-10-09T18:05:46Z</dc:date>
  <entry>
    <title>Flavonoid glycoside from &lt;i style=""&gt;Leucas lavandulaefolia&lt;/i&gt; (Rees) aerial parts</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/6646" />
    <author>
      <name>Chandrashekar, K S</name>
    </author>
    <author>
      <name>Arun, B J</name>
    </author>
    <author>
      <name>Satyanarayana, D</name>
    </author>
    <author>
      <name>Subramanyam, E V S</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/6646</id>
    <updated>2009-11-18T16:30:30Z</updated>
    <published>2006-08-01T00:00:00Z</published>
    <summary type="text">Title: Flavonoid glycoside from &lt;i style=""&gt;Leucas lavandulaefolia&lt;/i&gt; (Rees) aerial parts
Authors: Chandrashekar, K S; Arun, B J; Satyanarayana, D; Subramanyam, E V S
Abstract: Chrysoeriol-4'-&lt;i style=""&gt;O&lt;/i&gt;-&lt;img src='/image/spc_char/alpha.gif' border=0&gt;-L-rhamnopyranosyl (1→2) &lt;img src='/image/spc_char/beta.gif' border=0&gt;-D-galacto­pyranosyl (1→6) &lt;img src='/image/spc_char/beta.gif' border=0&gt;-D-glucopyranoside has been isolated from &lt;i style=""&gt;Leucas lavandulaefolia&lt;/i&gt; Rees aerial parts and its structure has been determined by UV-Vis, IR, &lt;sup&gt;1&lt;/sup&gt;H and &lt;sup&gt;13&lt;/sup&gt;C NMR and mass spectroscopic methods.
Page(s): 1968-1969</summary>
    <dc:date>2006-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis and microbiological evaluation of 2-acetanilido-4-arylthiazole derivatives</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/6643" />
    <author>
      <name>Pattan, S R</name>
    </author>
    <author>
      <name>Ali, M Shamrez</name>
    </author>
    <author>
      <name>Pattan, J S</name>
    </author>
    <author>
      <name>Purohit, S S</name>
    </author>
    <author>
      <name>Reddy, V V K</name>
    </author>
    <author>
      <name>Nataraj, B R</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/6643</id>
    <updated>2009-11-24T16:30:22Z</updated>
    <published>2006-08-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis and microbiological evaluation of 2-acetanilido-4-arylthiazole derivatives
Authors: Pattan, S R; Ali, M Shamrez; Pattan, J S; Purohit, S S; Reddy, V V K; Nataraj, B R
Abstract: A series of compounds have been synthesized by reacting 2-amino 4-arylthiazole with different substituted acetanilides and chloroacetylation of 2-amino 4-arylthiazole or their substituted derivatives. Ten different substituted compounds synthesized out of the 2-acetanilido 4-arylthiazole derivatives and 2-pyrazine 4-arylthiazole have been evaluated for the antifungal and antibacterial activities. These compounds have showed moderate antibacterial and very good activity.
Page(s): 1929-1932</summary>
    <dc:date>2006-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>A new route to the synthesis of long-chain methyl &lt;img src='/image/spc_char/alpha.gif' border=0&gt;-chlorooxoalkanoates</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/6642" />
    <author>
      <name>Rauf, Abdul</name>
    </author>
    <author>
      <name>Ahmad, Shabana</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/6642</id>
    <updated>2009-11-20T16:30:26Z</updated>
    <published>2006-08-01T00:00:00Z</published>
    <summary type="text">Title: A new route to the synthesis of long-chain methyl &lt;img src='/image/spc_char/alpha.gif' border=0&gt;-chlorooxoalkanoates
Authors: Rauf, Abdul; Ahmad, Shabana
Abstract: A reaction of long-chain methyl epoxyalkanoates with chlorotrimethylsilane in presence of triethylamine followed by Jones&lt;b style=""&gt;′&lt;/b&gt; oxidation has resulted in the formation of respective chlorooxo derivatives. The reaction proceeds under mild conditions and in a short span of time. Thus, one pot synthesis of methyl chlorooxoalkanoates is assisted with high purity and good yield of the products. The pure products are characterized by IR, &lt;sup&gt;1&lt;/sup&gt;H NMR, &lt;sup&gt;13&lt;/sup&gt;C NMR and MS spectra.
Page(s): 1924-1928</summary>
    <dc:date>2006-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis of model compounds for the investigation of biomarker’s thermal behaviour</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/6641" />
    <author>
      <name>Sirkecioğlu, Okan</name>
    </author>
    <author>
      <name>Karlığa, Bekir</name>
    </author>
    <author>
      <name>Talınlı, Naciye</name>
    </author>
    <author>
      <name>Snape, Colin</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/6641</id>
    <updated>2009-11-18T16:30:34Z</updated>
    <published>2006-08-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis of model compounds for the investigation of biomarker’s thermal behaviour
Authors: Sirkecioğlu, Okan; Karlığa, Bekir; Talınlı, Naciye; Snape, Colin
Abstract: The model compounds, which are used to investigate the organic structure and thermal behaviour of fossil fuels, have been synthesized starting from 4-hydroxybenzyl thiocholesterol, 4-hydroxybenzyl cholesterol and 4-hydroxybenzyl cholestanol.
Page(s): 1894-1899</summary>
    <dc:date>2006-08-01T00:00:00Z</dc:date>
  </entry>
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