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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/21473" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/21473</id>
  <updated>2026-10-09T21:54:30Z</updated>
  <dc:date>2026-10-09T21:54:30Z</dc:date>
  <entry>
    <title>Synthesis of biologically important new 1, 4-benzothiazines bearing thiazole substituted aroyl moiety</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/21567" />
    <author>
      <name>Ingle, R D</name>
    </author>
    <author>
      <name>Bhingolikar, V E</name>
    </author>
    <author>
      <name>Bondge, S P</name>
    </author>
    <author>
      <name>Mane, R A</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/21567</id>
    <updated>2013-10-16T16:35:40Z</updated>
    <published>2003-03-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis of biologically important new 1, 4-benzothiazines bearing thiazole substituted aroyl moiety
Authors: Ingle, R D; Bhingolikar, V E; Bondge, S P; Mane, R A
Abstract: 2-Acyl-4-(2'-methyl/phenyl/nicotinyl-thiazol-4'-yl)&#xD;
phenols &lt;b&gt;1&lt;/b&gt; have been obtained from the condensation of 2, 4-diacylphenol and&#xD;
thioamides in one pot using phenyl trimethyl ammonium tribromide(PTr). The&#xD;
compounds &lt;b&gt;1&lt;/b&gt; are then converted to their respective esters 2 by&#xD;
condensing with aroyl chlorides. The esters 2 are then subjected to B.V.&#xD;
transformation to yield l-phenyl-3-[2'-hydroxy-5'-(2"-substitutedthiazol-4'-yl)]phenylpropane-1,&#xD;
3-diones&#xD;
&#xD;
&lt;i&gt;3&lt;/i&gt;. These diones &lt;b&gt;3&lt;/b&gt; and&#xD;
2-aminobenzenethiol when allowed to react in DMSO afford the cyclocondensed&#xD;
products 2-[2'hydroxy-5'-(2" -substitutedthiazol-4" -yl)benzoyl]-3-(4'-substi&#xD;
tutedphenyl)-1, 4-benzothiazines &lt;b&gt;4&lt;/b&gt;. The structures of the new products &lt;b&gt;4&lt;/b&gt;&#xD;
have been confirmed by elemental and spectral methods. The results of the&#xD;
microbial screening of the compounds are also recorded.
Page(s): 695-698</summary>
    <dc:date>2003-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis of new 4-aryl/alkyl-1-(5',5'-diphenyl-4'-oxo-1&lt;i&gt;'&lt;/i&gt;-H-4&lt;i&gt;'&lt;/i&gt;,5&lt;i&gt;'&lt;/i&gt;-dihydroimidazolidin- 2&lt;i&gt;'&lt;/i&gt;-yl)-3-hydroxy-1,2,4-triazolidine-5-thione derivatives as potential anti-cancer agents</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/21566" />
    <author>
      <name>Datar, Prasanna A</name>
    </author>
    <author>
      <name>Shirodkar, P Y</name>
    </author>
    <author>
      <name>Panikkar, K R</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/21566</id>
    <updated>2013-10-10T16:37:48Z</updated>
    <published>2003-03-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis of new 4-aryl/alkyl-1-(5',5'-diphenyl-4'-oxo-1&lt;i&gt;'&lt;/i&gt;-H-4&lt;i&gt;'&lt;/i&gt;,5&lt;i&gt;'&lt;/i&gt;-dihydroimidazolidin- 2&lt;i&gt;'&lt;/i&gt;-yl)-3-hydroxy-1,2,4-triazolidine-5-thione derivatives as potential anti-cancer agents
Authors: Datar, Prasanna A; Shirodkar, P Y; Panikkar, K R
Abstract: New 4-aryl/alkyl-1-(5',5'-diphenyl-4'-oxo-1&lt;i&gt;'&lt;/i&gt;-H-4&lt;i&gt;'&lt;/i&gt;,5&lt;i&gt;'&lt;/i&gt;-dihydroimidazolidin-&#xD;
&#xD;
2&lt;i&gt;'&lt;/i&gt;-yl)-3-hydroxy-1,2,4-triazolidine-5-thiones&#xD;
&lt;b&gt;3&lt;/b&gt; have been prepared by the reaction of 2-carbethoxy-(5',5'-diphenyl-4&lt;i&gt;'&lt;/i&gt;oxo-1&lt;i&gt;'&lt;/i&gt;&#xD;
-H-4&lt;i&gt;'&lt;/i&gt;,5&lt;i&gt;'&lt;/i&gt;-dihydroimidazolidin-2&lt;i&gt;'&lt;/i&gt;-yl)-hydrazine &lt;b&gt;2&lt;/b&gt; with&#xD;
various aryl/alkylisothiocyanates. Their anti-bacterial, anti-fungal, anthelmintic&#xD;
and anti-cancer activities are reported.
Page(s): 690-694</summary>
    <dc:date>2003-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis and antibacterial activity of pyrimido[4,5&lt;i&gt;-b&lt;/i&gt;]quinolines</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/21565" />
    <author>
      <name>Kumar, R Nandha</name>
    </author>
    <author>
      <name>Suresh, T</name>
    </author>
    <author>
      <name>Mohan, P S</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/21565</id>
    <updated>2013-10-05T16:36:50Z</updated>
    <published>2003-03-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis and antibacterial activity of pyrimido[4,5&lt;i&gt;-b&lt;/i&gt;]quinolines
Authors: Kumar, R Nandha; Suresh, T; Mohan, P S
Abstract: A concise one-pot synthesis of pyrimido[4,5-&lt;i&gt;b&lt;/i&gt;]quinolines&#xD;
&lt;b&gt;3a-e&lt;/b&gt; has been achieved from the potential substrates 2-chloro-3-formylquinolines&#xD;
&lt;b&gt;1&lt;/b&gt; and guanidine nitrate &lt;b&gt;2&lt;/b&gt;. All the synthesized compounds have been&#xD;
biologically screened for their antibacterial activity.
Page(s): 688-689</summary>
    <dc:date>2003-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis of some benzothiazepins and their antimicrobial activities</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/21564" />
    <author>
      <name>Shetgiri, N P</name>
    </author>
    <author>
      <name>Nayak, B K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/21564</id>
    <updated>2013-10-06T16:34:45Z</updated>
    <published>2003-03-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis of some benzothiazepins and their antimicrobial activities
Authors: Shetgiri, N P; Nayak, B K
Abstract: A series of&#xD;
2-[(substitutedphenyl)-4-(substitutedphenyl)]-3,3-dihydro substituted-1 ,5-benzothiazepin&#xD;
&lt;b&gt;3&lt;/b&gt; has been synthesized starting from acetophenones. The compounds are&#xD;
characterized and screened for their antimicrobial activities.
Page(s): 683-687</summary>
    <dc:date>2003-03-01T00:00:00Z</dc:date>
  </entry>
</feed>

