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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.49B(08) [August 2010]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10074</link>
    <description />
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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/10089" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/10088" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/10087" />
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    <title>The Collection's search engine</title>
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    <link>http://nopr.niscair.res.in/simple-search</link>
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/10090">
    <title>A green approach in aqueous phase synthesis of isoxazolidine derivatives from N-phenyl-&lt;img src='/image/spc_char/alpha.gif' border=0&gt;-amino nitrone and their antibacterial activities</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10090</link>
    <description>Title: A green approach in aqueous phase synthesis of isoxazolidine derivatives from N-phenyl-&lt;img src='/image/spc_char/alpha.gif' border=0&gt;-amino nitrone and their antibacterial activities
&lt;br/&gt;
&lt;br/&gt;Authors: Chakraborty, Bhaskar; Chhetri, Manjit Singh; Samanta, Amalesh
&lt;br/&gt;
&lt;br/&gt;Abstract: 1,3 Dipolar&#xD;
cycloaddition reaction of N-phenyl-&lt;img src='/image/spc_char/alpha.gif' border=0&gt;-amino nitrone with different&#xD;
dipolarophiles have been studied in water for the synthesis of novel&#xD;
isoxazolidines. Significant change in rate acceleration and high yield of these&#xD;
reactions are observed in water compared to organic solvents. All the&#xD;
synthesized compounds have been screened for their antibacterial activity and&#xD;
found to exihibit significant activity.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1155-1160</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/10089">
    <title>Synthesis and biological evaluation of some innovative coumarin derivatives containing thiazolidin-4-one ring</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10089</link>
    <description>Title: Synthesis and biological evaluation of some innovative coumarin derivatives containing thiazolidin-4-one ring
&lt;br/&gt;
&lt;br/&gt;Authors: RamaGanesh, C K; Bodke, Yadav D; Venkatesh, K B
&lt;br/&gt;
&lt;br/&gt;Abstract: The reaction of ethyl&#xD;
2-oxo-2&lt;i&gt;H&lt;/i&gt;-chromene-3-carboxylate with hydrazine followed by condensation&#xD;
of the resulting hydrazone with different aromatic aldehydes give the&#xD;
corresponding Schiff bases &lt;b style=""&gt;5a-e&lt;/b&gt;. Reaction&#xD;
of these Schiff bases with mercaptoacetic acid furnishes the target&#xD;
thiazolidinone molecules &lt;b style=""&gt;6a-e&lt;/b&gt;. The&#xD;
newly synthesized compounds have been screened for antibacterial and analgesic&#xD;
activities.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1151-1154</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/10088">
    <title>Synthesis of isoxazolyl quinoline-3-carboxamides and 1,4-benzothiazine-2-carboxamides as potential bioactive compounds</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10088</link>
    <description>Title: Synthesis of isoxazolyl quinoline-3-carboxamides and 1,4-benzothiazine-2-carboxamides as potential bioactive compounds
&lt;br/&gt;
&lt;br/&gt;Authors: Rajanarendar, E; Murthy, K Rama; Reddy, M Nagi; Raju, S
&lt;br/&gt;
&lt;br/&gt;Abstract: Synthesis of&#xD;
isoxazolyl quinoline-3-carboxamides &lt;b style=""&gt;3&lt;/b&gt;&#xD;
and isoxazolyl-1,4-benzothiazine-2-carboxamides &lt;b style=""&gt;4&lt;/b&gt; have been accompli­shed by cyclocondensation of&#xD;
isoxazolyl-3-oxo-butanamides &lt;b style=""&gt;2&lt;/b&gt; with &lt;i style=""&gt;o&lt;/i&gt;-amino benzaldehyde or &lt;i style=""&gt;o&lt;/i&gt;-amino thiophenol involving&#xD;
Friedelander’s condensation and oxidative cyclization respectively.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1144-1150</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/10087">
    <title>Mixed ligand cobalt(II) complex as an efficient catalyst for oxidative deoximation using hydrogen peroxide</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10087</link>
    <description>Title: Mixed ligand cobalt(II) complex as an efficient catalyst for oxidative deoximation using hydrogen peroxide
&lt;br/&gt;
&lt;br/&gt;Authors: Das, Pranab J; Das, Amal; Baruah, Akashi
&lt;br/&gt;
&lt;br/&gt;Abstract: Mixed ligand&#xD;
cobalt(II) complexes having an amino acid as a ligand are reported to catalyze&#xD;
the decomposition of hydrogen peroxide. This property was utilized for carrying&#xD;
out an easy and efficient deoximation of oximes to the corresponding carbonyl&#xD;
compounds.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1140-1143</description>
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