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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.49B(01) [January 2010]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/7116</link>
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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/7145" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/7144" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/7143" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/7142" />
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/7145">
    <title>Synthesis of some novel chalcones of phthalimidoester possessing good anti-inflammatory and antimicrobial activity</title>
    <link>http://nopr.niscair.res.in/handle/123456789/7145</link>
    <description>Title: Synthesis of some novel chalcones of phthalimidoester possessing good anti-inflammatory and antimicrobial activity
&lt;br/&gt;
&lt;br/&gt;Authors: Gaikwad, Kishor V; Gaikwad, Sandip V; Jadhav, Satish B; Rathod, Shantilal D
&lt;br/&gt;
&lt;br/&gt;Abstract: A new series of methyl-2-[substituted benzylidine]-4-[2-(ph­thalimide) ethoxy] acetoacetate, &lt;b style=""&gt;5a-h&lt;/b&gt; have been synthesized from the combination of methyl-4-[2-(phthalimido) ethoxy] aceto­acetate, &lt;b style=""&gt;3 &lt;/b&gt;and substituted benzaldehyde &lt;b style=""&gt;4a-h&lt;/b&gt; which results in both anti-inflammatory and antimicrobial active compound. These compounds have been characterized by IR, &lt;sup&gt;1&lt;/sup&gt;H NMR, mass spectral and elemental analysis. These compounds have been subjected to preliminary anti-inflammatory screening using the carrageenan induced rat pow oedema model. Compounds &lt;b style=""&gt;5a,b,c &lt;/b&gt;show marked activity comparable to indomethacin. Compounds &lt;b style=""&gt;5a,b,c,g&lt;/b&gt;  show significant antimicrobial activity.
&lt;br/&gt;
&lt;br/&gt;Page(s): 131-136</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/7144">
    <title>A novel access to dispirocyclohexanoneindano pyrrolidines</title>
    <link>http://nopr.niscair.res.in/handle/123456789/7144</link>
    <description>Title: A novel access to dispirocyclohexanoneindano pyrrolidines
&lt;br/&gt;
&lt;br/&gt;Authors: Poornachandran, Mahalingam; Raghunathan, Raghavachary
&lt;br/&gt;
&lt;br/&gt;Abstract: Synthesis of a series of novel dispirocyclohexanoneindano pyrrolidines has been described. The cycloaddition reaction of azomethine ylide generated from ninhydrin and sarcosine with bisarylidenecyclohexanones was found to be highly region­selective.
&lt;br/&gt;
&lt;br/&gt;Page(s): 127-130</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/7143">
    <title>New cytotoxic saponin of &lt;i&gt;Albizzia lebbeck&lt;/i&gt;</title>
    <link>http://nopr.niscair.res.in/handle/123456789/7143</link>
    <description>Title: New cytotoxic saponin of &lt;i&gt;Albizzia lebbeck&lt;/i&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Jangwan, J S; Dobhal, Maneesha; Kumar, Naveen
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="metricconverter"&gt; The methanolic extract of the stem bark of &lt;i&gt;Albizzia lebbeck,&lt;/i&gt; a new cytotoxic saponin is isolated and characterized with the help of FABMS, &lt;sup&gt;13&lt;/sup&gt;C NMR and chemical studies. The isolated compound exhibited potent cytotoxic activity against human aqueous cell carcinoma [HSC-2 and HSC-3]. &lt;/smarttagtype&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 123-126</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/7142">
    <title>Synthesis of 1,3,5-triazinane-2-thiones and 1,3,5-oxadiazinane-4-thiones linked with isoxazoles</title>
    <link>http://nopr.niscair.res.in/handle/123456789/7142</link>
    <description>Title: Synthesis of 1,3,5-triazinane-2-thiones and 1,3,5-oxadiazinane-4-thiones linked with isoxazoles
&lt;br/&gt;
&lt;br/&gt;Authors: Rajanarendar, E; Reddy, A Siva Rami; Shaik, Firoz Pasha
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="metricconverter"&gt; Trimolecular condensation of &lt;i&gt;N&lt;/i&gt;-(3,5-dimethyl-4-isoxazolyl)-&lt;i&gt;N&lt;/i&gt;'-arylthioureas &lt;b&gt;2 &lt;/b&gt;obtained from&lt;b&gt; 1&lt;/b&gt; by reaction with aryliso­thiocyanates, with aqueous formaldehyde and primary amines in toluene under reflux leads to 5-alkyl-1-(3,5-dimethyl-4-iso­xa­zolyl)-3-aryl-hexahydro-1,3,5-triazinane-2-thiones&lt;b&gt; 3 &lt;/b&gt;in excellent yields. Condensation of &lt;b&gt;2 &lt;/b&gt;with aqueous formaldehyde under similar condition provides isoxazolyl 1,3,5-oxadiazinane-4-thiones &lt;b style=""&gt;4&lt;/b&gt;. &lt;/smarttagtype&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 119-122</description>
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