<?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.45B(08) [August 2006]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/6422</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/6646" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/6643" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/6642" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/6641" />
      </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/123456789/6646">
    <title>Flavonoid glycoside from &lt;i style=""&gt;Leucas lavandulaefolia&lt;/i&gt; (Rees) aerial parts</title>
    <link>http://nopr.niscair.res.in/handle/123456789/6646</link>
    <description>Title: Flavonoid glycoside from &lt;i style=""&gt;Leucas lavandulaefolia&lt;/i&gt; (Rees) aerial parts
&lt;br/&gt;
&lt;br/&gt;Authors: Chandrashekar, K S; Arun, B J; Satyanarayana, D; Subramanyam, E V S
&lt;br/&gt;
&lt;br/&gt;Abstract: Chrysoeriol-4'-&lt;i style=""&gt;O&lt;/i&gt;-&lt;img src='/image/spc_char/alpha.gif' border=0&gt;-L-rhamnopyranosyl (1→2) &lt;img src='/image/spc_char/beta.gif' border=0&gt;-D-galacto­pyranosyl (1→6) &lt;img src='/image/spc_char/beta.gif' border=0&gt;-D-glucopyranoside has been isolated from &lt;i style=""&gt;Leucas lavandulaefolia&lt;/i&gt; Rees aerial parts and its structure has been determined by UV-Vis, IR, &lt;sup&gt;1&lt;/sup&gt;H and &lt;sup&gt;13&lt;/sup&gt;C NMR and mass spectroscopic methods.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1968-1969</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/6643">
    <title>Synthesis and microbiological evaluation of 2-acetanilido-4-arylthiazole derivatives</title>
    <link>http://nopr.niscair.res.in/handle/123456789/6643</link>
    <description>Title: Synthesis and microbiological evaluation of 2-acetanilido-4-arylthiazole derivatives
&lt;br/&gt;
&lt;br/&gt;Authors: Pattan, S R; Ali, M Shamrez; Pattan, J S; Purohit, S S; Reddy, V V K; Nataraj, B R
&lt;br/&gt;
&lt;br/&gt;Abstract: A series of compounds have been synthesized by reacting 2-amino 4-arylthiazole with different substituted acetanilides and chloroacetylation of 2-amino 4-arylthiazole or their substituted derivatives. Ten different substituted compounds synthesized out of the 2-acetanilido 4-arylthiazole derivatives and 2-pyrazine 4-arylthiazole have been evaluated for the antifungal and antibacterial activities. These compounds have showed moderate antibacterial and very good activity.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1929-1932</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/6642">
    <title>A new route to the synthesis of long-chain methyl &lt;img src='/image/spc_char/alpha.gif' border=0&gt;-chlorooxoalkanoates</title>
    <link>http://nopr.niscair.res.in/handle/123456789/6642</link>
    <description>Title: A new route to the synthesis of long-chain methyl &lt;img src='/image/spc_char/alpha.gif' border=0&gt;-chlorooxoalkanoates
&lt;br/&gt;
&lt;br/&gt;Authors: Rauf, Abdul; Ahmad, Shabana
&lt;br/&gt;
&lt;br/&gt;Abstract: A reaction of long-chain methyl epoxyalkanoates with chlorotrimethylsilane in presence of triethylamine followed by Jones&lt;b style=""&gt;′&lt;/b&gt; oxidation has resulted in the formation of respective chlorooxo derivatives. The reaction proceeds under mild conditions and in a short span of time. Thus, one pot synthesis of methyl chlorooxoalkanoates is assisted with high purity and good yield of the products. The pure products are characterized by IR, &lt;sup&gt;1&lt;/sup&gt;H NMR, &lt;sup&gt;13&lt;/sup&gt;C NMR and MS spectra.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1924-1928</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/6641">
    <title>Synthesis of model compounds for the investigation of biomarker’s thermal behaviour</title>
    <link>http://nopr.niscair.res.in/handle/123456789/6641</link>
    <description>Title: Synthesis of model compounds for the investigation of biomarker’s thermal behaviour
&lt;br/&gt;
&lt;br/&gt;Authors: Sirkecioğlu, Okan; Karlığa, Bekir; Talınlı, Naciye; Snape, Colin
&lt;br/&gt;
&lt;br/&gt;Abstract: The model compounds, which are used to investigate the organic structure and thermal behaviour of fossil fuels, have been synthesized starting from 4-hydroxybenzyl thiocholesterol, 4-hydroxybenzyl cholesterol and 4-hydroxybenzyl cholestanol.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1894-1899</description>
  </item>
</rdf:RDF>

