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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.48B(07) [July 2009]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/5052</link>
    <description />
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      <title>A copper sulphate catalysed synthesis of derivatives of tetra substituted pyridine</title>
      <link>http://nopr.niscair.res.in/handle/123456789/5211</link>
      <description>Title: A copper sulphate catalysed synthesis of derivatives of tetra substituted pyridine
&lt;br/&gt;
&lt;br/&gt;Authors: Kidwai, Mazaahir; Priya
&lt;br/&gt;
&lt;br/&gt;Abstract: Copper sulphate has been found to be an effective catalyst in water-ethanol solvent system for the synthesis of various tetra-substituted pyridine derivatives &lt;i style=""&gt;via&lt;/i&gt; Michael addition of &lt;img src='/image/spc_char/beta.gif'&gt;-dicarbonyl compounds to &lt;i style=""&gt;&lt;img src='/image/spc_char/alpha.gif'&gt; &lt;/i&gt;,&lt;i style=""&gt;&lt;img src='/image/spc_char/beta.gif'&gt;&lt;/i&gt;-unsaturated oximes and subsequent ring closure.  A rapid synthesis of heterocycles by this methodology is ecofriendly in nature in addition to remarkably improved yield and reduced reaction times.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1045-1048</description>
      <pubDate>Sun, 28 Jun 2009 22:58:59 GMT</pubDate>
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    <item>
      <title>New coumarin diol from the plant, &lt;i&gt;Chloroxylon swietenia&lt;/i&gt; DC</title>
      <link>http://nopr.niscair.res.in/handle/123456789/5210</link>
      <description>Title: New coumarin diol from the plant, &lt;i&gt;Chloroxylon swietenia&lt;/i&gt; DC
&lt;br/&gt;
&lt;br/&gt;Authors: Rao, G Venkateswara; Rao, K Sambasiva; Annamalai, T; Mukhopadhyay, T
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="metricconverter"&gt; A new coumarin diol has been isolated along with three known coumarin compounds, 6,8-diprenylumbelliferone, bergapten and isopimpinellin from the chloroform fraction of the leaves of the plant,&lt;b&gt; &lt;/b&gt;&lt;i&gt;Chloroxylon swietenia&lt;/i&gt; DC&lt;b&gt;. &lt;/b&gt;The structure of new compound has been established as 6-(2′,3′-dihydroxy-3-methylbutyl)-8-prenylumbelliferone based on the spectral (UV, IR, &lt;sup&gt;1&lt;/sup&gt;H, &lt;sup&gt;13&lt;/sup&gt;C and 2D NMR and mass) data. &lt;/smarttagtype&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 1041-1044</description>
      <pubDate>Sun, 28 Jun 2009 22:58:59 GMT</pubDate>
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    <item>
      <title>Isolation and characterization of novel esters from aerial parts of &lt;i&gt;Tiliacora acuminata&lt;/i&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/5209</link>
      <description>Title: Isolation and characterization of novel esters from aerial parts of &lt;i&gt;Tiliacora acuminata&lt;/i&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Selvaraj, S Joseph; Alphonse, I; Britto, S John
&lt;br/&gt;
&lt;br/&gt;Abstract: Two novel esters octyl(benzoylamino)acetate and heptadeca-4-ene-acetate have been isolated from the aerial parts of both male and female plants of &lt;i style=""&gt;Tiliacora acuminata&lt;/i&gt;. The structures are confirmed by spectroscopic and analytical methods.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1038-1040</description>
      <pubDate>Sun, 28 Jun 2009 22:58:59 GMT</pubDate>
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    <item>
      <title>Synthesis and evaluation of some new substituted phenylthiazole derivatives and their antitubercular activity</title>
      <link>http://nopr.niscair.res.in/handle/123456789/5208</link>
      <description>Title: Synthesis and evaluation of some new substituted phenylthiazole derivatives and their antitubercular activity
&lt;br/&gt;
&lt;br/&gt;Authors: Pattan, Shashikant R; Bukitagar, Anand A; Pattan, Jayashri S; Kapadnis, B P; Jadhav, S G
&lt;br/&gt;
&lt;br/&gt;Abstract: A new series of substituted phenylthiazole derivatives have been synthesized and the structures of these compounds have been established on the basis of spectral and elemental analysis. All compounds&lt;b&gt; &lt;/b&gt;have been screened for antitubercular activity by Middle brook 7H9 agar medium against H&lt;sub&gt;37&lt;/sub&gt;Rv. strain. Most of these compounds have shown promising antitubercular activity.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1033-1037</description>
      <pubDate>Sun, 28 Jun 2009 22:58:59 GMT</pubDate>
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