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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.50B(11) [November 2011]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/13043</link>
    <description />
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      <title>A new modified synthetic method for preparation of N, N-dichlorocarbamates</title>
      <link>http://nopr.niscair.res.in/handle/123456789/13053</link>
      <description>Title: A new modified synthetic method for preparation of N, N-dichlorocarbamates
&lt;br/&gt;
&lt;br/&gt;Authors: Gutch, Pranav K; Singh, Ravindra; Suryanarayana, M V S
&lt;br/&gt;
&lt;br/&gt;Abstract: A rapid, efficient,&#xD;
economic and easy to scale method for the effective conversion of carbamates to&#xD;
corresponding &lt;i&gt;N,N-&lt;/i&gt;dichlorocarbamates by using calcium hypochlorite in&#xD;
acidic medium has been described. The transformation has been carried out at&#xD;
room temperature with high yield and purity with reduced reaction time.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1677-1679</description>
      <pubDate>Sat, 29 Oct 2011 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>A convenient synthesis of ethyl furo[2,3-&lt;i style=""&gt;h&lt;/i&gt;] flavone/chromone-8-carboxylates</title>
      <link>http://nopr.niscair.res.in/handle/123456789/13052</link>
      <description>Title: A convenient synthesis of ethyl furo[2,3-&lt;i style=""&gt;h&lt;/i&gt;] flavone/chromone-8-carboxylates
&lt;br/&gt;
&lt;br/&gt;Authors: Reddy, S Satyanarayana; Venkati, M; Rao, Y Jayaprakash; Sharma, Kamalesh K; Krupadanam, G L D
&lt;br/&gt;
&lt;br/&gt;Abstract: The reaction of&#xD;
8-formyl-7-hydroxyflavones/chromone &lt;b&gt;2a-i &lt;/b&gt;with diethyl bromomalonate in&#xD;
the presence of K&lt;sub&gt;2&lt;/sub&gt;CO&lt;sub&gt;3&lt;/sub&gt;/toluene and&#xD;
tetrabutylammoniumbromide (TBAB) as a phase transfer catalyst under nitrogen&#xD;
atmosphere affords ethyl furo[2,3-&lt;i style=""&gt;h&lt;/i&gt;]flavone-8-carboxylates&#xD;
&lt;b style=""&gt;3a-h &lt;/b&gt;and ethyl&#xD;
2-(2'-furyl)-3-methyl-furo[2,3-&lt;i style=""&gt;h&lt;/i&gt;]chromone-8-carboxylate&#xD;
&lt;b&gt;3i&lt;/b&gt;&lt;b style=""&gt; &lt;/b&gt;(Method A).&lt;b style=""&gt; &lt;/b&gt;The reaction of &lt;b style=""&gt;2a-i&lt;/b&gt; with ethyl bromo acetate in powdered K&lt;sub&gt;2&lt;/sub&gt;CO&lt;sub&gt;3&lt;/sub&gt;/dioxane affords the same products &lt;b&gt;3a-i &lt;/b&gt;(Method B).
&lt;br/&gt;
&lt;br/&gt;Page(s): 1671-1676</description>
      <pubDate>Sat, 29 Oct 2011 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>An efficient FeCl&lt;sub&gt;3&lt;/sub&gt; catalyzed synthesis of &lt;img src='http://www.niscair.res.in/jinfo/Beta.gif' border=0&gt;-keto enol ethers under solvent-free microwave irradiation condition</title>
      <link>http://nopr.niscair.res.in/handle/123456789/13051</link>
      <description>Title: An efficient FeCl&lt;sub&gt;3&lt;/sub&gt; catalyzed synthesis of &lt;img src='http://www.niscair.res.in/jinfo/Beta.gif' border=0&gt;-keto enol ethers under solvent-free microwave irradiation condition
&lt;br/&gt;
&lt;br/&gt;Authors: Lingaiah, B P Venkat; Yakaiah, T; Shekhar, A Chandra; Kumar, A Ravi; Sathaiah, G; Reddy, G Venkat; Narsaiah, B; Rao, P Shanthan
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;img src='http://www.niscair.res.in/jinfo/Beta.gif' border=0&gt;-Keto&#xD;
enol ethers from cyclic 1,3-diketones have been synthesized in very good yield&#xD;
under solvent-free microwave irradiation conditions from differently&#xD;
substituted alcohols and &lt;img src='http://www.niscair.res.in/jinfo/Beta.gif' border=0&gt;-diketones in presence of ferric chloride as&#xD;
catalyst.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1667-1670</description>
      <pubDate>Sat, 29 Oct 2011 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Synthesis of thiazolyl benzimidazoles and thiazolyl coumarins linked to isoxazole as possible biodynamic agents</title>
      <link>http://nopr.niscair.res.in/handle/123456789/13050</link>
      <description>Title: Synthesis of thiazolyl benzimidazoles and thiazolyl coumarins linked to isoxazole as possible biodynamic agents
&lt;br/&gt;
&lt;br/&gt;Authors: Rajanarendar, E; Murthy, K Rama; Reddy, M Nagi; Shaik, Firoz Pasha
&lt;br/&gt;
&lt;br/&gt;Abstract: A new series of linked&#xD;
heterocyclics, 5-(1&lt;i style=""&gt;H&lt;/i&gt;-benzo[&lt;i style=""&gt;d&lt;/i&gt;]imidazol-2-yl-methyl)-3-(3-methyl-5-[(&lt;i style=""&gt;E&lt;/i&gt;)-2-phenyl-1-ethenyl]-4-iso­xazol­yl)-2-aryl-1,3-thiazolan-4-ones&#xD;
&lt;b style=""&gt;4&lt;/b&gt; and 3-{3-methyl-5-[(&lt;i style=""&gt;E&lt;/i&gt;)-2-phenyl-1-ethenyl]-4-isoxazolyl}-5-(2-oxo-2&lt;i style=""&gt;H&lt;/i&gt;-3-chromenyl)-2-ar­yl-1,3-thiazolan-4-ones&#xD;
&lt;b style=""&gt;5&lt;/b&gt; have been synthesized by the cyclo­condensation&#xD;
of 4-benzalamino-3-methyl-5-styrylisoxazole &lt;b style=""&gt;2&lt;/b&gt; with mercapto succinic acid followed by cyclization with 1,2-phenylenediamines&#xD;
or salicylaldehydes. Structures of all the newly synthesized compounds &lt;b style=""&gt;3-5&lt;/b&gt; have been confirmed by spectral and&#xD;
micro analytical data.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1658-1666</description>
      <pubDate>Sat, 29 Oct 2011 22:58:59 GMT</pubDate>
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