<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns="http://purl.org/rss/1.0/" xmlns:taxo="http://purl.org/rss/1.0/modules/taxonomy/" xmlns:sy="http://purl.org/rss/1.0/modules/syndication/" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <channel>
    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.44B(09) [September 2005]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/8777</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/9192" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/9191" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/9190" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/9189" />
      </rdf:Seq>
    </items>
  </channel>
  <textInput>
    <title>The Collection's search engine</title>
    <description>Search the Channel</description>
    <name>search</name>
    <link>http://nopr.niscair.res.in/simple-search</link>
  </textInput>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/9192">
    <title>Phase transfer catalyzed synthesis under ultrasonic irradiation and bioactivity of &lt;i&gt;N&lt;sup&gt; &lt;/sup&gt;&lt;/i&gt;'-(4, 6-disubstituted-pyrimidin-2-yl)- &lt;i&gt;N&lt;/i&gt;-(5-aryl-2-furoyl)thiourea derivatives</title>
    <link>http://nopr.niscair.res.in/handle/123456789/9192</link>
    <description>Title: Phase transfer catalyzed synthesis under ultrasonic irradiation and bioactivity of &lt;i&gt;N&lt;sup&gt; &lt;/sup&gt;&lt;/i&gt;'-(4, 6-disubstituted-pyrimidin-2-yl)- &lt;i&gt;N&lt;/i&gt;-(5-aryl-2-furoyl)thiourea derivatives
&lt;br/&gt;
&lt;br/&gt;Authors: Ke, Shao-Yong; Wei, Tai-Bao; Xue, Si-Jia; Duan, Li-Ping; Li, Jing-Zhi
&lt;br/&gt;
&lt;br/&gt;Abstract: Ten new &lt;i&gt;N&lt;/i&gt;'-(4, 6-disubstituted-pyrimidin-2-yl)-&lt;i&gt;N&lt;/i&gt;-(5-aryl-2-furoyl)thioureas&#xD;
have been synthesized using PEG-400 as solid-liquid phase transfer catalyst&#xD;
under ultrasonic irradiation. Their structures were exactly confirmed by IR, &lt;sup&gt;1&lt;/sup&gt;H&#xD;
NMR and elemental analysis. The preliminary biological tests show that compound&#xD;
&lt;b&gt;7b&lt;/b&gt; has better inhibitory activities against root and stalk of&#xD;
dicotyledon plant (such as &lt;i&gt;Amaranthus retroflexus&lt;/i&gt; &lt;i&gt;L.&lt;/i&gt;) in higher concentration.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1957-1960</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/9191">
    <title>Microwave induced solvent – free synthesis of 1-aryl-2-(1&lt;i&gt;E&lt;/i&gt;)-arylvinyl- 4-arylmethylene-2-imidazolin-5-ones</title>
    <link>http://nopr.niscair.res.in/handle/123456789/9191</link>
    <description>Title: Microwave induced solvent – free synthesis of 1-aryl-2-(1&lt;i&gt;E&lt;/i&gt;)-arylvinyl- 4-arylmethylene-2-imidazolin-5-ones
&lt;br/&gt;
&lt;br/&gt;Authors: Maruthikumar, T Venkata; Reddy, V Prabhakar; Rao, P Hanumantha
&lt;br/&gt;
&lt;br/&gt;Abstract: A microwave – assisted&#xD;
synthesis of the title compounds under solvent-free conditions is described.&#xD;
The yields and reaction time period are noticeably improved in comparison with&#xD;
conventional methods.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1931-1932</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/9190">
    <title>Direct esterification of carboxylic acids with &lt;i style=""&gt;p&lt;/i&gt;-cresol catalysed by acid activated Indian bentonite</title>
    <link>http://nopr.niscair.res.in/handle/123456789/9190</link>
    <description>Title: Direct esterification of carboxylic acids with &lt;i style=""&gt;p&lt;/i&gt;-cresol catalysed by acid activated Indian bentonite
&lt;br/&gt;
&lt;br/&gt;Authors: Vijayakumar, B; Iyengar, Pushpa; Nagendrappa, Gopalpur; Prakash, B S Jai
&lt;br/&gt;
&lt;br/&gt;Abstract: Acid activated Indian&#xD;
bentonite (AAIB) catalyst is used for the first time to esterify various&#xD;
carboxylic acids with &lt;i style=""&gt;p&lt;/i&gt;-cresol in&#xD;
average to excellent yields. Optimisation studies have been carried out for &lt;i style=""&gt;p&lt;/i&gt;-cresyl stearate synthesis. The&#xD;
catalyst is recoverable and recyclable.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1950-1953</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/9189">
    <title>Anthraquinone glycoside from stem bark, fatty acids and sterols from seeds of &lt;i&gt;Cassia reingera&lt;/i&gt;</title>
    <link>http://nopr.niscair.res.in/handle/123456789/9189</link>
    <description>Title: Anthraquinone glycoside from stem bark, fatty acids and sterols from seeds of &lt;i&gt;Cassia reingera&lt;/i&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Ledwani, Lalita; Singh, Mukhtar
&lt;br/&gt;
&lt;br/&gt;Abstract: From the bark of &lt;i&gt;Cassia&#xD;
reingera&lt;/i&gt; 1,5,6-trihydroxy-3-methyl-anthraquinone-8-O-&lt;img src='/image/spc_char/alpha.gif' border=0&gt;-L-glucoside has been isolated and its&#xD;
structure elucidated with the help of chemical studies and spectral data. The&#xD;
dyeing property of crude anthraquinone has been studied to develop variety of&#xD;
shades on wool by using different mordants. Sterols and fatty acids have been&#xD;
isolated from the seeds of &lt;i&gt;Cassia reingera&lt;/i&gt; and are identified by using&#xD;
GLC techniques by comparison with authentic sample.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1970-1971</description>
  </item>
</rdf:RDF>

