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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/6004" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/6004</id>
  <updated>2026-10-09T03:18:20Z</updated>
  <dc:date>2026-10-09T03:18:20Z</dc:date>
  <entry>
    <title>A facile one-pot synthetic route to substituted fused tetrahydropyrimidines. Part 41: Synthesis of 1-(aralkyl/aryl)-3- (alkyl/aralkyl/aryl)-5-oxo-l,2,3,4,5,6,7,8-octahydroquinazolines and 1-(aralkyl/aryl)-3- (alkyl/aralkyl/aryl)-7,7-dimethyl-5-oxo- 1,2,3,4,5,6,7,8-octahydroquinazolines</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/30693" />
    <author>
      <name>Chanda, Kaushik</name>
    </author>
    <author>
      <name>Dutta, Milan C</name>
    </author>
    <author>
      <name>Vishwakanna, Jai N</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/30693</id>
    <updated>2016-07-20T05:39:16Z</updated>
    <published>2006-04-01T00:00:00Z</published>
    <summary type="text">Title: A facile one-pot synthetic route to substituted fused tetrahydropyrimidines. Part 41: Synthesis of 1-(aralkyl/aryl)-3- (alkyl/aralkyl/aryl)-5-oxo-l,2,3,4,5,6,7,8-octahydroquinazolines and 1-(aralkyl/aryl)-3- (alkyl/aralkyl/aryl)-7,7-dimethyl-5-oxo- 1,2,3,4,5,6,7,8-octahydroquinazolines
Authors: Chanda, Kaushik; Dutta, Milan C; Vishwakanna, Jai N
Abstract: &lt;span style="mso-bidi-language:HI"&gt;A facile one pot pathway has been developed for&#xD;
the synthesis of novel 1-(aralkyl/aryl)-3-(alky/aralkyl/aryl)-5-oxo-1,2,3,4,5,6,7,8-octahydroquinazolirles&#xD;
&lt;b&gt;2a-e&lt;/b&gt; and 1-(aralkyl/aryl)-3-(alkyl/aralkyl/ary1)-7,7-dimethy1-5-oxo-1,2.3,4,5,6,7.8-&#xD;
&#xD;
&lt;span style="mso-bidi-language:HI"&gt;octahydroquinazolines &lt;b&gt;2f-k&lt;/b&gt; by the&#xD;
cyclocondensation of cyclic enaminones &lt;b&gt;la-d&lt;/b&gt; with formaldehyde and&#xD;
primary amines in refluxing methanol in good yields.&#xD;
&#xD;
&lt;/span&gt;&lt;/span&gt;
Page(s): 1076-1079</summary>
    <dc:date>2006-04-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Rapid and efficient microwave-assisted synthesis of 4-amino-3-mercapto- 5-substituted-1,2,4-triazoles</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/10578" />
    <author>
      <name>Joshi, S S</name>
    </author>
    <author>
      <name>Karnik, A V</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/10578</id>
    <updated>2010-11-13T16:31:06Z</updated>
    <published>2006-04-01T00:00:00Z</published>
    <summary type="text">Title: Rapid and efficient microwave-assisted synthesis of 4-amino-3-mercapto- 5-substituted-1,2,4-triazoles
Authors: Joshi, S S; Karnik, A V
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.
Page(s): 1057-1059</summary>
    <dc:date>2006-04-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>An efficient procedure for the synthesis of 1,1-diacetates from aldehydes with acetic anhydride catalyzed by silica sulfate</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/10577" />
    <author>
      <name>Jin, Tong-Shou</name>
    </author>
    <author>
      <name>Zhao, Ying</name>
    </author>
    <author>
      <name>Gu, Shu-Qing</name>
    </author>
    <author>
      <name>Liu, Li-Bin</name>
    </author>
    <author>
      <name>Li, Tong-Shuang</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/10577</id>
    <updated>2010-11-11T06:12:02Z</updated>
    <published>2006-04-01T00:00:00Z</published>
    <summary type="text">Title: An efficient procedure for the synthesis of 1,1-diacetates from aldehydes with acetic anhydride catalyzed by silica sulfate
Authors: Jin, Tong-Shou; Zhao, Ying; Gu, Shu-Qing; Liu, Li-Bin; Li, Tong-Shuang
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.
Page(s): 1054-1056</summary>
    <dc:date>2006-04-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Microwave-assisted solvent-free Friedlander synthesis of 1,8-naphthyridines using ammonium acetate as catalyst</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/10576" />
    <author>
      <name>Mogilaiah, K</name>
    </author>
    <author>
      <name>Rani, J Uma</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/10576</id>
    <updated>2010-11-12T16:30:38Z</updated>
    <published>2006-04-01T00:00:00Z</published>
    <summary type="text">Title: Microwave-assisted solvent-free Friedlander synthesis of 1,8-naphthyridines using ammonium acetate as catalyst
Authors: Mogilaiah, K; Rani, J Uma
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.
Page(s): 1051-1053</summary>
    <dc:date>2006-04-01T00:00:00Z</dc:date>
  </entry>
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