<?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.48B(08) [August 2009]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/5733</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/5792" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/5791" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/5790" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/5789" />
      </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/123456789/5792">
    <title>Reaction of 3-aminocyclohex-2-en-1-ones with arylidenemalononitriles: Synthesis, characterization and antimicrobial activity of some new quinoline bearing pyrazole nucleus</title>
    <link>http://nopr.niscair.res.in/handle/123456789/5792</link>
    <description>Title: Reaction of 3-aminocyclohex-2-en-1-ones with arylidenemalononitriles: Synthesis, characterization and antimicrobial activity of some new quinoline bearing pyrazole nucleus
&lt;br/&gt;
&lt;br/&gt;Authors: Shah, Nirav K; Patel, Manish P; Patel, Ranjan G
&lt;br/&gt;
&lt;br/&gt;Abstract: A new series of quinoline bearing pyrazole nucleus &lt;b style=""&gt;D&lt;sub&gt;1-36&lt;/sub&gt;&lt;/b&gt; have been prepared in one pot by condensing various arylidenemalononitriles &lt;b style=""&gt;A&lt;sub&gt;1-3&lt;/sub&gt;&lt;/b&gt; and 3-aminocyclohex-2-en-1-ones &lt;b style=""&gt;B&lt;sub&gt;1-12&lt;/sub&gt;&lt;/b&gt; in alcohol and in the presence of catalytic amount of piperidine. All the compounds have been characterized by their percentage yield, melting point, elemental analysis, &lt;sup&gt;1&lt;/sup&gt;H NMR and &lt;sup&gt;13&lt;/sup&gt;C NMR spectra and IR spectra. These compounds have been screened for their antimicrobial activities&lt;i style=""&gt;.&lt;/i&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 1170-1173</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/5791">
    <title>Tetraethylammonium superoxide induced Michael addition of active methylene compounds to chalcones</title>
    <link>http://nopr.niscair.res.in/handle/123456789/5791</link>
    <description>Title: Tetraethylammonium superoxide induced Michael addition of active methylene compounds to chalcones
&lt;br/&gt;
&lt;br/&gt;Authors: Raghuvanshi, Raghvendra Singh; Singh, Krishna Nand
&lt;br/&gt;
&lt;br/&gt;Abstract: Michael addition of active methylene compounds to chalcones using &lt;i style=""&gt;in-situ&lt;/i&gt; generated tetraethylammonium superoxide results in the formation of Michael adducts in 69-84% yield under mild reaction conditions, at room temperature.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1161-1163</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/5790">
    <title>Synthesis and characterization of 5-(2-nitro-1-arylpropyl)-4-aryl-1,2,3-selenadiazoles</title>
    <link>http://nopr.niscair.res.in/handle/123456789/5790</link>
    <description>Title: Synthesis and characterization of 5-(2-nitro-1-arylpropyl)-4-aryl-1,2,3-selenadiazoles
&lt;br/&gt;
&lt;br/&gt;Authors: Saravanan, S; Amuthavalli, A; Muthusubramanian, S
&lt;br/&gt;
&lt;br/&gt;Abstract: The synthesis&lt;b style=""&gt; &lt;/b&gt;and characterization of new 5-(2-nitro-1-arylpropyl)&lt;b style=""&gt;-&lt;/b&gt;4-aryl-1,2,3-selenadiazoles, obtained from the &lt;img src='/image/spc_char/alpha.gif'&gt;-functionalised semicarbazones are described. The structures of these compounds have been established by &lt;sup&gt;1&lt;/sup&gt;H and &lt;sup&gt;13&lt;/sup&gt;C NMR spectral data.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1144-1147</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/5789">
    <title>Synthesis of some novel barbituric acid and 1,3-cyclohexanedione based condensed  heterocycles</title>
    <link>http://nopr.niscair.res.in/handle/123456789/5789</link>
    <description>Title: Synthesis of some novel barbituric acid and 1,3-cyclohexanedione based condensed  heterocycles
&lt;br/&gt;
&lt;br/&gt;Authors: Sachar, Anand; Gupta, Poonam; Gupta, Shallu; Sharma, R L
&lt;br/&gt;
&lt;br/&gt;Abstract: Synthesis of some novel condensed heterocycles based on peripheral barbituric acid/1,3-cyclohexanedione moieties and central pyran, pyridine and thiin (thiopyran) ring systems has been achieved by the condensation of barbituric acid/1,3-cyclo­hexane­dione with different aromatic aldehydes.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1187-1194</description>
  </item>
</rdf:RDF>

