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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.48B(08) [August 2009]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/5733</link>
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      <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>
      <pubDate>Wed, 29 Jul 2009 22:58:59 GMT</pubDate>
    </item>
    <item>
      <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>
      <pubDate>Wed, 29 Jul 2009 22:58:59 GMT</pubDate>
    </item>
    <item>
      <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>
      <pubDate>Wed, 29 Jul 2009 22:58:59 GMT</pubDate>
    </item>
    <item>
      <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>
      <pubDate>Wed, 29 Jul 2009 22:58:59 GMT</pubDate>
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