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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.49B(07) [July 2010]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/9925</link>
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      <title>Microwave assisted transformation of benzimidazolyl chalcones into N&lt;sup&gt;1&lt;/sup&gt;-substituted pyrazolines and evaluation of their antimicrobial activities</title>
      <link>http://nopr.niscair.res.in/handle/123456789/9938</link>
      <description>Title: Microwave assisted transformation of benzimidazolyl chalcones into N&lt;sup&gt;1&lt;/sup&gt;-substituted pyrazolines and evaluation of their antimicrobial activities
&lt;br/&gt;
&lt;br/&gt;Authors: Rajora, Jayanti; Yadav, Janardan; Kumar, Ravindra; Srivastava, Yogendra K
&lt;br/&gt;
&lt;br/&gt;Abstract: 1-Benzimidazolyl-3-aryl-prop-2-ene-1-ones &lt;b style=""&gt;2&lt;/b&gt; have been transformed into N&lt;sup&gt;1&lt;/sup&gt;-substituted pyrazoline&#xD;
derivatives by the interaction with phenyl hydrazine, thiosemicarbazide and&#xD;
hydrazine hydrate in the presence of formic acid under solvent free microwave&#xD;
induced protocol. The structure of newly synthesized compounds have been&#xD;
confirmed on the basis of their elemental analysis and spectral data. Newly&#xD;
synthesized compounds have been evaluated for their antimicrobial activity &lt;i style=""&gt;in vitro&lt;/i&gt; against &lt;i style=""&gt;E. coli, K. pneumonae, P. aeruginosa &lt;/i&gt;and&lt;i style=""&gt; B. subtilis &lt;/i&gt;using paper&lt;i style=""&gt; &lt;/i&gt;disc&#xD;
method. Some of the compounds have shown significant activity against the&#xD;
pathogens.
&lt;br/&gt;
&lt;br/&gt;Page(s): 989-993</description>
      <pubDate>Mon, 28 Jun 2010 22:58:59 GMT</pubDate>
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    <item>
      <title>Designing hydroxy-functionalized chiral salen ligand and its use in the synthesis of dioxadiazasilamacroheterocycles</title>
      <link>http://nopr.niscair.res.in/handle/123456789/9937</link>
      <description>Title: Designing hydroxy-functionalized chiral salen ligand and its use in the synthesis of dioxadiazasilamacroheterocycles
&lt;br/&gt;
&lt;br/&gt;Authors: Singh, M S; Singh, Pratibha; Gupta, Ashutosh
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="metricconverter"&gt;&#xD;
&#xD;
&#xD;
&#xD;
Synthesis of&#xD;
dioxadiazasilamacroheterocycles is described. The key step involves the initial&#xD;
synthesis of symmetrical hydroxyl-functionalized chiral salen ligand, &lt;i style=""&gt;N&lt;/i&gt;,&lt;i style=""&gt;N&lt;/i&gt;′-bis(2-hydroxyacetophenonylidene)-1,2-diaminocyclohexane followed by sequential deprotonation with NaH to form dianion&#xD;
intermediate &lt;i style=""&gt;in situ&lt;/i&gt;, which reacts&#xD;
with diorganodichlorosilanes to furnish desired heterocycles. The products have&#xD;
been characterized by satisfactory elemental analyses and spectral (IR, &lt;sup&gt;1&lt;/sup&gt;H,&#xD;
&lt;sup&gt;13&lt;/sup&gt;C,&#xD;
&lt;sup&gt;29&lt;/sup&gt;Si NMR and mass) studies.&#xD;
&#xD;
&lt;/smarttagtype&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 985-988</description>
      <pubDate>Mon, 28 Jun 2010 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>A facile Ph&lt;sub&gt;3&lt;/sub&gt;P/CO&lt;sub&gt;2&lt;/sub&gt; mediated, one-pot synthesis of 2-oxazolidinones from 1,2-azido alcohols &lt;i style=""&gt;via&lt;/i&gt; phosphazene and isocyanate intermediates</title>
      <link>http://nopr.niscair.res.in/handle/123456789/9936</link>
      <description>Title: A facile Ph&lt;sub&gt;3&lt;/sub&gt;P/CO&lt;sub&gt;2&lt;/sub&gt; mediated, one-pot synthesis of 2-oxazolidinones from 1,2-azido alcohols &lt;i style=""&gt;via&lt;/i&gt; phosphazene and isocyanate intermediates
&lt;br/&gt;
&lt;br/&gt;Authors: Madhusudhan, G; Reddy, M Srinivasa; Reddy, Y Narayana; Vijayalakshmi, V; Suribabu, M; Balraju, V
&lt;br/&gt;
&lt;br/&gt;Abstract: A facile, efficient and&#xD;
convenient method has been developed for the one-pot synthesis of 2-oxazolidinones&#xD;
from the corresponding 1,2-azido alcohols &lt;i style=""&gt;via&lt;/i&gt;&#xD;
phosphazene and isocyanate intermediates in presence of Ph&lt;sub&gt;3&lt;/sub&gt;P/CO&lt;sub&gt;2&lt;/sub&gt;&#xD;
in toluene.
&lt;br/&gt;
&lt;br/&gt;Page(s): 978-984</description>
      <pubDate>Mon, 28 Jun 2010 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Synthesis and antimicrobial screening of some 3-[4-(3-aryl-1-phenyl-1&lt;i style=""&gt;H&lt;/i&gt;-pyrazol- 4-yl)-6-aryl-pyridin-2-yl] and 4-methyl- 3-phenyl-6-[4-(3-aryl-1-phenyl-1&lt;i style=""&gt;H&lt;/i&gt;-pyrazol-4-yl)-6-aryl-pyridin-2-yl] coumarins</title>
      <link>http://nopr.niscair.res.in/handle/123456789/9935</link>
      <description>Title: Synthesis and antimicrobial screening of some 3-[4-(3-aryl-1-phenyl-1&lt;i style=""&gt;H&lt;/i&gt;-pyrazol- 4-yl)-6-aryl-pyridin-2-yl] and 4-methyl- 3-phenyl-6-[4-(3-aryl-1-phenyl-1&lt;i style=""&gt;H&lt;/i&gt;-pyrazol-4-yl)-6-aryl-pyridin-2-yl] coumarins
&lt;br/&gt;
&lt;br/&gt;Authors: Brahmbhatt, D I; Kaneria, Ankit R; Patel, Anil K; Patel, Niraj H
&lt;br/&gt;
&lt;br/&gt;Abstract: Various 3-[4-(3-aryl-1-phenyl-1&lt;i style=""&gt;H&lt;/i&gt;-pyrazol-4-yl)-6-aryl-pyri­din-2-yl] coumarins &lt;b style=""&gt;4a-l&lt;/b&gt; and&#xD;
4-methyl-3-phenyl-6-[4-(3-aryl-1-phenyl-1&lt;i style=""&gt;H&lt;/i&gt;-pyrazol-4-yl)-6-aryl-pyridin-2-yl] coumarins &lt;b style=""&gt;5a-f&lt;/b&gt;&amp;nbsp; have been synthesized by reacting&#xD;
3-coumarinoylmethyl pyridi­nium bromides &lt;b style=""&gt;1a,b&lt;/b&gt;&#xD;
and 4-methyl-3-phenyl-6-coumarinoylmethyl pyridinium bromide &lt;b style=""&gt;2&lt;/b&gt; with pyrazolyl chalcones &lt;b style=""&gt;3a-f&lt;/b&gt; respectively under Krohnke’s&#xD;
reaction conditions. All the synthesized compounds &lt;b style=""&gt;4a-l&lt;/b&gt; and &lt;b style=""&gt;5a-f&lt;/b&gt; have been&#xD;
screened for their antibacterial activity against &lt;i style=""&gt;Escherichia coli&lt;/i&gt; (Gram -ve bacteria), &lt;i style=""&gt;Bacillus subtillis&lt;/i&gt; (Gram +ve bacteria) and antifungal activity&#xD;
against &lt;i style=""&gt;Candida albican&lt;/i&gt; (Fungi).
&lt;br/&gt;
&lt;br/&gt;Page(s): 971-977</description>
      <pubDate>Mon, 28 Jun 2010 22:58:59 GMT</pubDate>
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