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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.49B(02) [February 2010]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/7355</link>
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      <title>Ecofriendly synthesis of thieno[2,3-&lt;i style=""&gt;b&lt;/i&gt;]pyridines  derivativies</title>
      <link>http://nopr.niscair.res.in/handle/123456789/7370</link>
      <description>Title: Ecofriendly synthesis of thieno[2,3-&lt;i style=""&gt;b&lt;/i&gt;]pyridines  derivativies
&lt;br/&gt;
&lt;br/&gt;Authors: Kidwai, M; Priya; Poddar, R
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="PersonName"&gt; In order to avoid the use of too much organic solvent and harmful catalysts, 2-aminothiophenes are readily transformed to thieno­pyridines by an ecofriendly synthesis in a suitable solvent system. This reaction in aqueous medium and under microwave irradiation takes lesser time and results in higher yield as compared to conventional method.&lt;b style=""&gt;&lt;/b&gt; &lt;/smarttagtype&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 270-273</description>
      <pubDate>Fri, 29 Jan 2010 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Synthesis of benzofuran analogs of fenamates as non steroidal antiinflammatory agents</title>
      <link>http://nopr.niscair.res.in/handle/123456789/7369</link>
      <description>Title: Synthesis of benzofuran analogs of fenamates as non steroidal antiinflammatory agents
&lt;br/&gt;
&lt;br/&gt;Authors: Mane, Balasaheb Y; Agasimundin, Y S; Shivakumar, B
&lt;br/&gt;
&lt;br/&gt;Abstract: A series of benzofuran analogs of anthranilic acid derivatives are synthesized. All the new compounds have been characterized by spectral data and elemental analyses and screened for antiinflammatory activity. Compounds &lt;b style=""&gt;3e&lt;/b&gt;, &lt;b style=""&gt;4e&lt;/b&gt;,&lt;b style=""&gt; 4g &lt;/b&gt;and&lt;b style=""&gt; 5g&lt;/b&gt; are found to possess antiinflammatory activity comparable to that of standard diclofenac sodium
&lt;br/&gt;
&lt;br/&gt;Page(s): 264-269</description>
      <pubDate>Fri, 29 Jan 2010 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>A new route for the synthesis of (&lt;i style=""&gt;R&lt;/i&gt;)-glyceraldehyde acetonide: A key chiral building block</title>
      <link>http://nopr.niscair.res.in/handle/123456789/7368</link>
      <description>Title: A new route for the synthesis of (&lt;i style=""&gt;R&lt;/i&gt;)-glyceraldehyde acetonide: A key chiral building block
&lt;br/&gt;
&lt;br/&gt;Authors: Babu, K Chandra; Ramadasu, G; Gangaiah, L; Madhusudhan, G; Mukkanti, K
&lt;br/&gt;
&lt;br/&gt;Abstract: A new route for the synthesis of (&lt;i style=""&gt;R&lt;/i&gt;)-glyceraldehyde acetonide &lt;i style=""&gt;via&lt;/i&gt; asymmetric dihydroxylation of allyl 4-methoxybenzoate using the (DHQ)&lt;sub&gt;2&lt;/sub&gt;PHAL, K&lt;sub&gt;2&lt;/sub&gt;OsO&lt;sub&gt;4&lt;/sub&gt;·2H&lt;sub&gt;2&lt;/sub&gt;O catalyst system is described. This route involves the asymmetric dihydroxylation of allyl 4-methoxybenzoate, acetonide protection of vicinyl dihydroxyl groups followed by cleavage of &lt;i style=""&gt;p&lt;/i&gt;-methoxybenzoate ester and subsequent oxidation to give the (&lt;i style=""&gt;R&lt;/i&gt;)-glyceraldehyde acetonide.
&lt;br/&gt;
&lt;br/&gt;Page(s): 260-263</description>
      <pubDate>Fri, 29 Jan 2010 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>New constituents from &lt;i style=""&gt;Psoralea corylifolia&lt;/i&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/7367</link>
      <description>Title: New constituents from &lt;i style=""&gt;Psoralea corylifolia&lt;/i&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Tewari, Amit; Bhakuni, R S
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="metricconverter"&gt; Two new metabolites, named psoralester &lt;b style=""&gt;1&lt;/b&gt; and psorachromene &lt;b style=""&gt;2&lt;/b&gt;, a &lt;i&gt;trans&lt;/i&gt; isomer of bavachromene together with five known compounds have been isolated from the seeds of &lt;i style=""&gt;Psoralea corylifolia&lt;/i&gt; L. and characterized on the basis of their detailed NMR and mass spectral data. Psoralester possess a ten- membered lactone moiety and a long chain ester. &lt;/smarttagtype&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 256-259</description>
      <pubDate>Fri, 29 Jan 2010 22:58:59 GMT</pubDate>
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