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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.45B(04) [April 2006]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/6004</link>
    <description />
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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/10578" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/10577" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/10576" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/10575" />
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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/123456789/10578">
    <title>Rapid and efficient microwave-assisted synthesis of 4-amino-3-mercapto- 5-substituted-1,2,4-triazoles</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10578</link>
    <description>Title: Rapid and efficient microwave-assisted synthesis of 4-amino-3-mercapto- 5-substituted-1,2,4-triazoles
&lt;br/&gt;
&lt;br/&gt;Authors: Joshi, S S; Karnik, A V
&lt;br/&gt;
&lt;br/&gt;Abstract: Synthesis of 4-amino-3-mercapto-5-substituted-1,2,4-triazoles 3a-g, building blocks for the synthesis of fused heterocycles, under microwave irradiation is demonstrated.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1057-1059</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/10577">
    <title>An efficient procedure for the synthesis of 1,1-diacetates from aldehydes with acetic anhydride catalyzed by silica sulfate</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10577</link>
    <description>Title: An efficient procedure for the synthesis of 1,1-diacetates from aldehydes with acetic anhydride catalyzed by silica sulfate
&lt;br/&gt;
&lt;br/&gt;Authors: Jin, Tong-Shou; Zhao, Ying; Gu, Shu-Qing; Liu, Li-Bin; Li, Tong-Shuang
&lt;br/&gt;
&lt;br/&gt;Abstract: The reac tion of aldehyde with acetic anhydride catalyzed by silica sulfate results in 1,1-diac etates in high yield at room&#xD;
temperature.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1054-1056</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/10576">
    <title>Microwave-assisted solvent-free Friedlander synthesis of 1,8-naphthyridines using ammonium acetate as catalyst</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10576</link>
    <description>Title: Microwave-assisted solvent-free Friedlander synthesis of 1,8-naphthyridines using ammonium acetate as catalyst
&lt;br/&gt;
&lt;br/&gt;Authors: Mogilaiah, K; Rani, J Uma
&lt;br/&gt;
&lt;br/&gt;Abstract: The microwave enhanced synthes is of 1,8-naphthyridines 3 is achieved rapidly and in good yield via the Friedlander condensation of 2-aminonicotinaldehyde 1 with carbonyl compounds containing &lt;img src='/image/spc_char/alpha.gif' border=0&gt; -methylene group 2 in the presence of ammonium acetate.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1051-1053</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/10575">
    <title>Solvent free &lt;i&gt;N&lt;/i&gt;-alkylation of phenyl sulfanilides under microwave irradiation</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10575</link>
    <description>Title: Solvent free &lt;i&gt;N&lt;/i&gt;-alkylation of phenyl sulfanilides under microwave irradiation
&lt;br/&gt;
&lt;br/&gt;Authors: Jaisankar, P; Srinivasan, P C
&lt;br/&gt;
&lt;br/&gt;Abstract: A facile &lt;i&gt;N&lt;/i&gt;-alkylation&#xD;
of phenylsulfanilides by reaction with &#xD;
primary alkyl halides (benzyl bromide, ethyl bromoacetate and n-butyl bromide)in the presence of anhydrous potassium carbonate under microwave condition to give &lt;i&gt;N&lt;/i&gt;-alkylated products in good yields is reported
&lt;br/&gt;
&lt;br/&gt;Page(s): 1048-1050</description>
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