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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.48B(09) [September 2009]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/6040</link>
    <description />
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      <title>An efficient synthesis of &lt;img src='/image/spc_char/alpha.gif'&gt;-(alkylidene)-5, 5-dimethyl-&lt;img src='/image/spc_char/delta1.gif'&gt;-lactones</title>
      <link>http://nopr.niscair.res.in/handle/123456789/6068</link>
      <description>Title: An efficient synthesis of &lt;img src='/image/spc_char/alpha.gif'&gt;-(alkylidene)-5, 5-dimethyl-&lt;img src='/image/spc_char/delta1.gif'&gt;-lactones
&lt;br/&gt;
&lt;br/&gt;Authors: Parsekar, Sonia B; Amonkar, Chandan P; Nadkarni, Vishnu S; Tilve, Santosh G
&lt;br/&gt;
&lt;br/&gt;Abstract: 2-(-Alkylidene&#xD;
substituted)-5,5-dimethyl-&lt;img src='/image/spc_char/delta1.gif'&gt;-lactones have been synthesized in two steps. The&#xD;
stable phosphorane carboethoxy­methyledene (&lt;img src='/image/spc_char/alpha.gif'&gt;-prenyl)-triphenylphosphorane is&#xD;
condensed with different carbonyl compounds to afford &lt;img src='/image/spc_char/alpha.gif'&gt;,&lt;img src='/image/spc_char/beta.gif'&gt;-unsaturated esters&#xD;
which are cyclised using PPA to give title compounds
&lt;br/&gt;
&lt;br/&gt;Page(s): 1333-1336</description>
      <pubDate>Sat, 29 Aug 2009 22:58:59 GMT</pubDate>
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    <item>
      <title>A facile microwave assisted synthesis of flavones</title>
      <link>http://nopr.niscair.res.in/handle/123456789/6067</link>
      <description>Title: A facile microwave assisted synthesis of flavones
&lt;br/&gt;
&lt;br/&gt;Authors: Menezes, M J; Manjrekar, S; Pai, V; Patre, R E; Tilve, S G
&lt;br/&gt;
&lt;br/&gt;Abstract: Chalcones &lt;b style=""&gt;3a-f&lt;/b&gt; on irradiation under microwave in&#xD;
DMSO in presence of catalytic amount of I&lt;sub&gt;2&lt;/sub&gt; provides flavones &lt;b style=""&gt;4a-f&lt;/b&gt; in high yield. The corresponding&#xD;
chalcones &lt;b style=""&gt;3a-f&lt;/b&gt; are obtained by&#xD;
Claisen-Schimdt condensation of aromatic aldehydes with &lt;i style=""&gt;o&lt;/i&gt;-hydroxy acetophenone
&lt;br/&gt;
&lt;br/&gt;Page(s): 1311-1314</description>
      <pubDate>Sat, 29 Aug 2009 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Enzyme catalyzed acylation of 7-hydroxy-4-methyl-2H-chromene-2-one using microwave</title>
      <link>http://nopr.niscair.res.in/handle/123456789/6066</link>
      <description>Title: Enzyme catalyzed acylation of 7-hydroxy-4-methyl-2H-chromene-2-one using microwave
&lt;br/&gt;
&lt;br/&gt;Authors: Kidwai, Mazaahir; Mothsra, Poonam; Poddar, Roona
&lt;br/&gt;
&lt;br/&gt;Abstract: Acylation of&#xD;
pharmacologically important 7-hydroxy-4-methyl-2&lt;i style=""&gt;H&lt;/i&gt;-chromene-2-one has been investigated in the presence of&#xD;
immobilized lipase under the influence of microwave. Commercially available&#xD;
lipase (Novozyme 435) under microwave leads to enhancement in rate of reaction&#xD;
in comparison with conventional heating in immobilized lipase catalyzed&#xD;
acylation with various acids. Different microwave assisted technologies were&#xD;
studied and compared. This paper investigates the synergism between enzyme&#xD;
catalysis and microwaves on acylation of 7-hydroxy-4-methyl-2&lt;i style=""&gt;H&lt;/i&gt;-chromene-2-one, with different acids&#xD;
using lipase Novozyme 435
&lt;br/&gt;
&lt;br/&gt;Page(s): 1307-1310</description>
      <pubDate>Sat, 29 Aug 2009 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Simple and convenient methods for synthesis, resolution and application of aminonaphthols</title>
      <link>http://nopr.niscair.res.in/handle/123456789/6065</link>
      <description>Title: Simple and convenient methods for synthesis, resolution and application of aminonaphthols
&lt;br/&gt;
&lt;br/&gt;Authors: Periasamy, Mariappan; Anwar, Shaik; Reddy, Meda Narsi
&lt;br/&gt;
&lt;br/&gt;Abstract: Racemic&#xD;
aminonaphthols are obtained in 70-95% yield by simple and straightforward&#xD;
condensation of benzaldehyde, 2-naphthol and 1° or 2° amines in ethanol solvent&#xD;
under refluxing conditions. The racemic aminonaphthols&#xD;
1-(α-aminobenzyl)-2-naphthol and 1-(α-pyrrolidinylbenzyl)-2-naphthol have been&#xD;
resolved using l&lt;i&gt;-(+)&lt;/i&gt;-tartaric&#xD;
acid. The racemic 1-(α-&lt;i&gt;N&lt;/i&gt;-butylaminobenzyl)-2-naphthol and&#xD;
1-(α-piperidylbenzyl)-2-naphthol have been resolved using &lt;i&gt;R&lt;/i&gt;-(+)-BINOL&#xD;
and boric acid. The racemic (2-methoxynaphth-1-yl)benzylamine is resolved using&#xD;
dibenzoyl-l-(-)-tartaric&#xD;
acid. The readiliy accessible chiral aminonaphthols are useful for resolution&#xD;
of important moieties like racemic BINOL, ibuprofen and mandelic acid
&lt;br/&gt;
&lt;br/&gt;Page(s): 1261-1273</description>
      <pubDate>Sat, 29 Aug 2009 22:58:59 GMT</pubDate>
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