<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns="http://purl.org/rss/1.0/" xmlns:taxo="http://purl.org/rss/1.0/modules/taxonomy/" xmlns:sy="http://purl.org/rss/1.0/modules/syndication/" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <channel>
    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.44B(01) [January 2005]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/8769</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/8937" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/8936" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/8935" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/8934" />
      </rdf:Seq>
    </items>
  </channel>
  <textInput>
    <title>The Collection's search engine</title>
    <description>Search the Channel</description>
    <name>search</name>
    <link>http://nopr.niscair.res.in/simple-search</link>
  </textInput>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/8937">
    <title>A convenient synthesis of Nabumetone-An anti-inflammatory drug candidate</title>
    <link>http://nopr.niscair.res.in/handle/123456789/8937</link>
    <description>Title: A convenient synthesis of Nabumetone-An anti-inflammatory drug candidate
&lt;br/&gt;
&lt;br/&gt;Authors: Srinivasulu, G; Reddy, A Raghupathi; Nagaraju, Ch; Reddy, P Pratap; Reddy, M Satyanarayana
&lt;br/&gt;
&lt;br/&gt;Abstract: A facile and industrially&#xD;
viable approach to Nabumetone (an anti-inflammatory agent) is reported.
&lt;br/&gt;
&lt;br/&gt;Page(s): 207-208</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/8936">
    <title>Reduction of aldehydes and oximes to their corresponding alcohols and amines by catalytic hydrogenation method</title>
    <link>http://nopr.niscair.res.in/handle/123456789/8936</link>
    <description>Title: Reduction of aldehydes and oximes to their corresponding alcohols and amines by catalytic hydrogenation method
&lt;br/&gt;
&lt;br/&gt;Authors: Basappa; Doreswamy, B H; Mahendra, M; Mantelingu, K; Sridhar, M A; Prasad, J Shashidhara; Rangappa, K S
&lt;br/&gt;
&lt;br/&gt;Abstract: The reduction of aldehydes such as&#xD;
2-butyl-5-chloro-3&lt;i style=""&gt;H&lt;/i&gt;-imidazole-5-carbaldehyde&#xD;
and veratraldehyde, which are pharmaceutical key intermediates, have been&#xD;
reduced to alcohols by catalytic hydrogenation method in the presence of&#xD;
magnesium and also oximes are reduced to primary amines successively by&#xD;
magnesium/ammonium formate system, is a large scale feasible and cheaper&#xD;
method. The crystal structure of the product, (2-butyl-5-chloro-3&lt;i style=""&gt;H&lt;/i&gt;-imidazole-4-yl)-methanol &lt;b style=""&gt;1&lt;/b&gt; is reported.
&lt;br/&gt;
&lt;br/&gt;Page(s): 148-151</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/8935">
    <title>Synthesis of 2-aryl-7-(3-oxo-2&lt;i&gt;H&lt;/i&gt;-[1,4]-benzoxazin-6-yl)pyrazolo[1,5-&lt;i style=""&gt;&lt;img src='/image/spc_char/alpha.gif' border=0&gt; &lt;/i&gt;]pyrimidines as potential COX-2-inhibitors</title>
    <link>http://nopr.niscair.res.in/handle/123456789/8935</link>
    <description>Title: Synthesis of 2-aryl-7-(3-oxo-2&lt;i&gt;H&lt;/i&gt;-[1,4]-benzoxazin-6-yl)pyrazolo[1,5-&lt;i style=""&gt;&lt;img src='/image/spc_char/alpha.gif' border=0&gt; &lt;/i&gt;]pyrimidines as potential COX-2-inhibitors
&lt;br/&gt;
&lt;br/&gt;Authors: Reddy, G Jagath; Sailaja, S; Rao, K Srinivasa
&lt;br/&gt;
&lt;br/&gt;Abstract: A series of&#xD;
2-aryl-7-(3-oxo-2&lt;i style=""&gt;H&lt;/i&gt;-[1,4]-benzoxazin-6-yl)­pyra­zo­lo­[1,5-&lt;i style=""&gt;&lt;img src='/image/spc_char/alpha.gif' border=0&gt; &lt;/i&gt;]pyrimidines (&lt;b style=""&gt;8a&lt;/b&gt;-&lt;b style=""&gt;d&lt;/b&gt; and &lt;b style=""&gt;9a&lt;/b&gt;-&lt;b style=""&gt;d&lt;/b&gt;)&#xD;
have been synthe­sized and evaluated for COX-2-inhibitor activity.
&lt;br/&gt;
&lt;br/&gt;Page(s): 204-206</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/8934">
    <title>A mild and efficient method for the acetylation of alcohols</title>
    <link>http://nopr.niscair.res.in/handle/123456789/8934</link>
    <description>Title: A mild and efficient method for the acetylation of alcohols
&lt;br/&gt;
&lt;br/&gt;Authors: Shirini, F; Zolfigol, M A; Safari, A
&lt;br/&gt;
&lt;br/&gt;Abstract: The acetylation of&#xD;
alcohols has been carried out efficiently in the presence of a catalytic amount&#xD;
of Zr(HSO&lt;sub&gt;4&lt;/sub&gt;)&lt;sub&gt;4&lt;/sub&gt;. All reactions are performed at room&#xD;
temperature and under heterogeneous conditions in good to high yields.
&lt;br/&gt;
&lt;br/&gt;Page(s): 201-203</description>
  </item>
</rdf:RDF>

