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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.50B(08) [August 2011]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12482</link>
    <description />
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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/12520" />
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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/12518" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/12517" />
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12520">
    <title>Synthesis and anticancer activity of some new series of 1, 4-dihydropyridine derivatives</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12520</link>
    <description>Title: Synthesis and anticancer activity of some new series of 1, 4-dihydropyridine derivatives
&lt;br/&gt;
&lt;br/&gt;Authors: Kumar, R Surendra; Idhayadhulla, A; Nasser, A Jamal Abdul; Murali, K
&lt;br/&gt;
&lt;br/&gt;Abstract: A series of 1,4-dihydropyridine derivatives &lt;b&gt;1a-c&lt;/b&gt; have been prepared from 4-substituted&#xD;
aromatic aldehyde, ethyl acetoacetate and ammonium hydroxide following Hantzsch&#xD;
method. The compounds &lt;b&gt;1a-c&lt;/b&gt; have been reacted with semicarbazide to give&#xD;
the compounds&lt;b&gt; 2a-c&lt;/b&gt;. The compounds &lt;b&gt;1a-c&lt;/b&gt; have been reacted with&#xD;
thiosemicarbazide to give the compounds&lt;b&gt; 3a-c&lt;/b&gt;. The structures of&#xD;
synthesized compounds are confirmed by IR, ¹H and ¹³C NMR, mass spectrometry&#xD;
and elemental analyses. The newly synthesized compounds have been screened for&#xD;
preliminary anti-cancer activity against HepG2 (Liver), Hela (Cervical) and&#xD;
MCF-7 (Breast) cancer cells. The compound &lt;b&gt;2a&lt;/b&gt; is highly&#xD;
active against HepG2, MCF-7 and &lt;b&gt;3a&lt;/b&gt; is highly active against Hela&#xD;
(Cervical) and these have been selected for advanced preclinical development.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1140-1144</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12519">
    <title>Chemical composition and antimicrobial activity of the essential oil from the rhizome of &lt;i style=""&gt;Canna indica&lt;/i&gt; Linn</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12519</link>
    <description>Title: Chemical composition and antimicrobial activity of the essential oil from the rhizome of &lt;i style=""&gt;Canna indica&lt;/i&gt; Linn
&lt;br/&gt;
&lt;br/&gt;Authors: Indrayan, A K; Bhojak, N K; Kumar, Nikhil; Shatru, Ajat; Gaur, Abhishek
&lt;br/&gt;
&lt;br/&gt;Abstract: The essential oil of&#xD;
the rhizome of &lt;i style=""&gt;Canna indica&lt;/i&gt; Linn. (yellow&#xD;
flower variety) has been isolated by hydrodistillation and analysed by GC and&#xD;
GC/MS. Forty-three compounds representing 95.32% of the oil have been&#xD;
identified. The sesquiterpene hydrocarbons and their derivatives form the major&#xD;
part (52.56%). The major terpene/terpenoid constituents of the essential oil of&#xD;
rhizome are &lt;img src='/image/spc_char/gamma2.gif' border=0&gt;-eudesmol (9.79%), δ-cadinol (6.33%), &lt;img src='/image/spc_char/gamma2.gif' border=0&gt;-selinene (5.23%) and&#xD;
luciferin (5.05%). Surprisingly, certain fatty acids are also found to be&#xD;
present in noticeable amount, palmitic acid (8.53%) being the main. The oil&#xD;
showed good antibacterial activity against &lt;i style=""&gt;Staphylococcus&#xD;
aureus&lt;/i&gt; but mild activity against &lt;i style=""&gt;Bacillus&#xD;
subtilis&lt;/i&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 1136-1139</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12518">
    <title>An efficient and simple synthesis of tetraketones catalyzed by Yb(OTf)&lt;sub&gt;3&lt;/sub&gt;-SiO&lt;sub&gt;2&lt;/sub&gt; under solvent free conditions</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12518</link>
    <description>Title: An efficient and simple synthesis of tetraketones catalyzed by Yb(OTf)&lt;sub&gt;3&lt;/sub&gt;-SiO&lt;sub&gt;2&lt;/sub&gt; under solvent free conditions
&lt;br/&gt;
&lt;br/&gt;Authors: Rao, V Kameshwara; Kumar, Muthyala Manoj; Kumar, Anil
&lt;br/&gt;
&lt;br/&gt;Abstract: A novel and efficient&#xD;
three-component one-pot condensation method has been described for the&#xD;
synthesis of tetraketones or arylmethylene[&lt;i style=""&gt;bis&lt;/i&gt;(3-hydroxy-2-cyclohexene-1-ones)]&#xD;
using Yb(OTf)&lt;sub&gt;3&lt;/sub&gt;-SiO&lt;sub&gt;2&lt;/sub&gt; and amine as catalytic system under&#xD;
solvent free conditions. Tetraketones are obtained in high yield (73-88%). The&#xD;
application of an eco-friendly, non-corrosive, and reusable catalytic system&#xD;
makes this method advantageous.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1128-1135</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/12517">
    <title>A simple and efficient bromoazidation of alkenes using PTT and TMSN&lt;sub&gt;3&lt;/sub&gt; in ionic liquid</title>
    <link>http://nopr.niscair.res.in/handle/123456789/12517</link>
    <description>Title: A simple and efficient bromoazidation of alkenes using PTT and TMSN&lt;sub&gt;3&lt;/sub&gt; in ionic liquid
&lt;br/&gt;
&lt;br/&gt;Authors: Kumar, Anil; Rao, M Sudershan; Mehta, Vibhor
&lt;br/&gt;
&lt;br/&gt;Abstract: A simple and efficient&#xD;
one-pot method has been described for the bromoazidation of alkenes using&#xD;
phenyltrimethylammonium tribromide (PTT) and TMSN&lt;sub&gt;3&lt;/sub&gt; in ionic liquid.&#xD;
The bromoazides have been obtained in good to excellent yield from various&#xD;
alkenes such as styrenes, chalcones, and cycloalkenes at room temperature.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1123-1127</description>
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