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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.44B(04) [April 2005]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/8772</link>
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      <title>Isolation and hypotensive activity of five new phytoconstituents from chloroform extract of flowers of &lt;i&gt;H&lt;/i&gt;&lt;i style=""&gt;ibiscus rosasinensis&lt;/i&gt; Linn.</title>
      <link>http://nopr.niscair.res.in/handle/123456789/9002</link>
      <description>Title: Isolation and hypotensive activity of five new phytoconstituents from chloroform extract of flowers of &lt;i&gt;H&lt;/i&gt;&lt;i style=""&gt;ibiscus rosasinensis&lt;/i&gt; Linn.
&lt;br/&gt;
&lt;br/&gt;Authors: Siddiqui, Anees A; Wani, Sachin M; Rajesh, R; Alagarsamy, V
&lt;br/&gt;
&lt;br/&gt;Abstract: Three extracts of &lt;i style=""&gt;Hibiscus rosasinensis &lt;/i&gt;Linn have been prepared and studied for their&#xD;
hypotensive activity. Hydroalcoholic extract is found to exhibit prominent&#xD;
activity when compared to the reference standard minoxidil followed by&#xD;
chloroform extract. In an attempt to isolate the active constituents&#xD;
responsible for this activity, five new phytoconstituents have been isolated&#xD;
and their structures are elucidated from spectral evidence (IR, NMR and mass&#xD;
spectra). Hypotensive activity of these compounds is also studied.
&lt;br/&gt;
&lt;br/&gt;Page(s): 806-811</description>
      <pubDate>Tue, 29 Mar 2005 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Synthesis of novel naphtho[2,1-&lt;i style=""&gt;b&lt;/i&gt;]furo pyrazolyl, isoxazolyl and pyridyl derivatives as potential antimicrobial agents</title>
      <link>http://nopr.niscair.res.in/handle/123456789/9001</link>
      <description>Title: Synthesis of novel naphtho[2,1-&lt;i style=""&gt;b&lt;/i&gt;]furo pyrazolyl, isoxazolyl and pyridyl derivatives as potential antimicrobial agents
&lt;br/&gt;
&lt;br/&gt;Authors: Mahadevan, K M; Basavaraj, K M; Mathias, D A Prathima; Vaidya, V P
&lt;br/&gt;
&lt;br/&gt;Abstract: The treatment of chalcones &lt;b&gt;2a-f&lt;/b&gt; with substituted hydrazines in ethanol results&#xD;
in the formation of 3-(3-aminonaphtho[2,1-&lt;i style=""&gt;b&lt;/i&gt;]fur-2-yl)-5-arylpyrazolines&#xD;
&lt;b style=""&gt;3a-l&lt;/b&gt;.The reaction of these&#xD;
chalcones &lt;b&gt;2a-f &lt;/b&gt;&lt;b style=""&gt; &lt;/b&gt;with hydroxylamine hydrochloride in&#xD;
presence of catalytic amount of hydrochloric acid affords&#xD;
3-(3-aminonaphtho[2,1-&lt;i style=""&gt;b&lt;/i&gt;]fur-2-yl)-5-arylisoxazolines&#xD;
&lt;b&gt;4a-f&lt;/b&gt;. The synthesis of another biheterocycle,&#xD;
2-amino-3-cyano-4-aryl-6-(3-aminonaphtho[2,1-&lt;i style=""&gt;b&lt;/i&gt;]fur-2yl)pyridines &lt;b&gt;5a-f&lt;/b&gt; is accomplished by reacting&#xD;
chalcones &lt;b&gt;2a-f &lt;/b&gt; with malanonitrile&#xD;
in presence of ammonium acetate. All the newly synthesized compounds are&#xD;
characterized by elemental analysis and spectral studies, and evaluated for&#xD;
antimicrobial activity.
&lt;br/&gt;
&lt;br/&gt;Page(s): 789-793</description>
      <pubDate>Tue, 29 Mar 2005 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Synthesis of biogenetically possible 2-phenyl-4-oxopyrano[2,3-&lt;i style=""&gt;&lt;img src='/image/spc_char/alpha.gif' border=0&gt;&lt;/i&gt;]carbazoles</title>
      <link>http://nopr.niscair.res.in/handle/123456789/9000</link>
      <description>Title: Synthesis of biogenetically possible 2-phenyl-4-oxopyrano[2,3-&lt;i style=""&gt;&lt;img src='/image/spc_char/alpha.gif' border=0&gt;&lt;/i&gt;]carbazoles
&lt;br/&gt;
&lt;br/&gt;Authors: Vandana, T; Prasad, K J Rajendra
&lt;br/&gt;
&lt;br/&gt;Abstract: Synthesis of&#xD;
2-cinnamoyl-1-hydroxycarbazoles &lt;b style=""&gt;2&lt;/b&gt; by&#xD;
the condensation of 1-hydroxycarbazoles with aluminium chloride and&#xD;
phosphorousoxy chloride in good yield followed by acid catalysed cyclisation and&#xD;
dehydrogenation with DDQ to obtain the biogenetically possible&#xD;
2-phenyl-4-oxopyrano[2,3-&lt;i style=""&gt;&lt;img src='/image/spc_char/alpha.gif' border=0&gt; &lt;/i&gt;]carbazoles&#xD;
&lt;b style=""&gt;4 &lt;/b&gt;is described.
&lt;br/&gt;
&lt;br/&gt;Page(s): 819-822</description>
      <pubDate>Tue, 29 Mar 2005 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Synthesis and pharmacological evaluation of heterocycles from benzocycloheptenones</title>
      <link>http://nopr.niscair.res.in/handle/123456789/8999</link>
      <description>Title: Synthesis and pharmacological evaluation of heterocycles from benzocycloheptenones
&lt;br/&gt;
&lt;br/&gt;Authors: Venkateswarlu, Peesapati; Vasireddy, Nageswara Rao
&lt;br/&gt;
&lt;br/&gt;Abstract: A new series of benzocyclohepten-5-one&#xD;
thiosemicarbazones &lt;b style=""&gt;2a,b&lt;/b&gt; obtained by&#xD;
condensation of benzocyclohepten-5-ones &lt;b style=""&gt;1a,b&lt;/b&gt;&#xD;
with thiosemicarbazide, are treated with monochloroacetic acid,&#xD;
3-bromopropionic acid, chloroacetyl chloride, 1,3-dichloroacetone, phenacyl&#xD;
bromide and acetic anhydride, respectively to yield nitrogen and sulphur&#xD;
containing heterocycles. The structures of all these compounds have been&#xD;
determined by analytical and spectral methods. A few of them exhibit promising&#xD;
antibacterial activity.
&lt;br/&gt;
&lt;br/&gt;Page(s): 783-788</description>
      <pubDate>Tue, 29 Mar 2005 22:58:59 GMT</pubDate>
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