<?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:dc="http://purl.org/dc/elements/1.1/">
  <channel rdf:about="http://nopr.niscpr.res.in/handle/123456789/56992">
    <title>NOPR Community:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/56992</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/57569" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/57568" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/57567" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/57566" />
      </rdf:Seq>
    </items>
    <dc:date>2026-10-05T10:48:39Z</dc:date>
  </channel>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/57569">
    <title>Photohalogenation of 3-acetylcoumarins: Facile synthesis of 3-(2-amino-4-thiazolyl)coumarins and their conversion into 3-[2,5- dimethylpyrrol-1-yl) thiazol-4-yI]-coumanns</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/57569</link>
    <description>Title: Photohalogenation of 3-acetylcoumarins: Facile synthesis of 3-(2-amino-4-thiazolyl)coumarins and their conversion into 3-[2,5- dimethylpyrrol-1-yl) thiazol-4-yI]-coumanns
Authors: Vardhan, V Aditya; Rao, V Rajeshwar
Page(s): 1085-1088</description>
    <dc:date>1997-12-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/57568">
    <title>Kinetic and mechanistic aspects of acid-catalysed hydrolysis of hydroxamic acids</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/57568</link>
    <description>Title: Kinetic and mechanistic aspects of acid-catalysed hydrolysis of hydroxamic acids
Authors: Ghosh, Kallol K
Page(s): 1089-1102</description>
    <dc:date>1997-12-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/57567">
    <title>Chemoselective rhodium-carbenoid reaction with the aromatic nucleus: An efficient methodology for 2-indanones, 2- tetralones and 2-benzosuberones and its application in the synthesis of (±)-ar-Himachalene</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/57567</link>
    <description>Title: Chemoselective rhodium-carbenoid reaction with the aromatic nucleus: An efficient methodology for 2-indanones, 2- tetralones and 2-benzosuberones and its application in the synthesis of (±)-ar-Himachalene
Authors: Sudrik, S G; Nanjundiah, B S; Sonawane, H R
Page(s): 1103-1112</description>
    <dc:date>1997-12-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/57566">
    <title>Expeditious synthetic route to B-ring functionalised 2-oxa-steroids: Synthesis of 17-ethylenedioxy-6a-hydroxy-2-oxa-4-androsten-3-one as key synthon</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/57566</link>
    <description>Title: Expeditious synthetic route to B-ring functionalised 2-oxa-steroids: Synthesis of 17-ethylenedioxy-6a-hydroxy-2-oxa-4-androsten-3-one as key synthon
Authors: Nangia, Ashwini; Anthony, A
Page(s): 1113-1118</description>
    <dc:date>1997-12-01T00:00:00Z</dc:date>
  </item>
</rdf:RDF>

