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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/319" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/319</id>
  <updated>2026-10-10T12:32:40Z</updated>
  <dc:date>2026-10-10T12:32:40Z</dc:date>
  <entry>
    <title>Al₂O₃ catalyzed Friedlander synthesis of 1, 8-naphthyridines in the solid state</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/756" />
    <author>
      <name>Mogilaiah, K</name>
    </author>
    <author>
      <name>Vidya, K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/756</id>
    <updated>2008-04-07T04:30:25Z</updated>
    <published>2007-10-01T00:00:00Z</published>
    <summary type="text">Title: Al₂O₃ catalyzed Friedlander synthesis of 1, 8-naphthyridines in the solid state
Authors: Mogilaiah, K; Vidya, K
Abstract: Al₂O₃ catalyzes efficiently the Freidlander condensation of &#xD;
2-aminonicotinaldehyde 1 with various carbonyl compounds containing ⍺-methylene group 2 in the solid state to afford the corresponding 1,8-naphthyridines 3. The reaction proceeds efficiently at room temperature in good yields and in a state of high purity.
Page(s): 1721-1723</summary>
    <dc:date>2007-10-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Clay-catalyzed high-speed synthesis of thiadiazepine in one-pot</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/754" />
    <author>
      <name>Siddiqui, Ibadur R</name>
    </author>
    <author>
      <name>Singh, Pravin K</name>
    </author>
    <author>
      <name>Srivastava, Vishal</name>
    </author>
    <author>
      <name>Singh, J</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/754</id>
    <updated>2008-04-08T04:30:17Z</updated>
    <published>2007-10-01T00:00:00Z</published>
    <summary type="text">Title: Clay-catalyzed high-speed synthesis of thiadiazepine in one-pot
Authors: Siddiqui, Ibadur R; Singh, Pravin K; Srivastava, Vishal; Singh, J
Abstract: Microwave assisted clay-catalyzed solid state integrated chemical process which enables the consumption of toxic inter-mediates and their isolation from environment, reduce reaction time, cost and complex isolation procedures enhances yields are effective for realizing a green chemical process in library synthe-ses of bio-active compounds. This is described here in the synthe-sis of thiadiazepine. Antifungal screening results on Fusarium oxysporum and Penicillium citrinum show that most of the syn-thesized compounds display promising antifungal activity, compa-rable with griseofulvin and dithane M-45 as standards.
Page(s): 1716-1720</summary>
    <dc:date>2007-10-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Dehydroacetic acid and its derivatives in organic synthesis: Synthesis of some new 2-substituted-4- (5-bromo-4-hydroxy-6-methyl- 2H-pyran-2-one-3-yl)thiazoles</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/752" />
    <author>
      <name>Prakash, Richa Prakash</name>
    </author>
    <author>
      <name>Kumar, Ajay</name>
    </author>
    <author>
      <name>Singh, Shiv P</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/752</id>
    <updated>2008-06-06T05:44:12Z</updated>
    <published>2007-10-01T00:00:00Z</published>
    <summary type="text">Title: Dehydroacetic acid and its derivatives in organic synthesis: Synthesis of some new 2-substituted-4- (5-bromo-4-hydroxy-6-methyl- 2H-pyran-2-one-3-yl)thiazoles
Authors: Prakash, Richa Prakash; Kumar, Ajay; Singh, Shiv P
Abstract: Synthesis of 3 β,3β,5-tribromoacetyl-4-hydroxy-6- methyl-2H-pyran-2-one 2 from the bromination of DHA 1 in chloroform has been reported. The reaction of 2 with various thioureas/thioamides leads to an efficient synthesis of new 2-substituted-4-(5-bromo-4-hydroxy-6-methyl- 2H-pyran-2-one-3-yl)thiazoles.
Page(s): 1713-1715</summary>
    <dc:date>2007-10-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis and studies of some novel s-triazine based aminopyrimidines, isoxazoles and 1,5-benzothiazepines</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/751" />
    <author>
      <name>Solankee, Anjani</name>
    </author>
    <author>
      <name>Kapadia, Kishor</name>
    </author>
    <author>
      <name>Solankee, Pankit</name>
    </author>
    <author>
      <name>Prajapati, Yogesh</name>
    </author>
    <author>
      <name>Patel, Hiral</name>
    </author>
    <author>
      <name>Solankee, Sejal</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/751</id>
    <updated>2008-04-08T04:30:14Z</updated>
    <published>2007-10-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis and studies of some novel s-triazine based aminopyrimidines, isoxazoles and 1,5-benzothiazepines
Authors: Solankee, Anjani; Kapadia, Kishor; Solankee, Pankit; Prajapati, Yogesh; Patel, Hiral; Solankee, Sejal
Abstract: An elegant synthesis of the titled compounds 7a-e, 8a-e and 9a-e have been presented starting from chalcones 6a-e based on &#xD;
s-triazine nucleus. These chalcones 6a-e on cyclisation with guanidine nitrate and hydroxylamine hydrochloride in the presence of alkali give aminopyrimidines 7a-e and isoxazoles 8a-e respectively. Further these chalcones 6a-e on cyclisation with &#xD;
2-aminothiophenol in the presence of few drops of glacial acetic acid give 1,5-benzothiazepines 9a-e. All the products obtained from these reactions are characterized by elemental analysis, IR, ¹H NMR and mass spectral data.
Page(s): 1707-1712</summary>
    <dc:date>2007-10-01T00:00:00Z</dc:date>
  </entry>
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