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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/6471</link>
    <description />
    <pubDate>Wed, 07 Oct 2026 22:08:18 GMT</pubDate>
    <dc:date>2026-10-07T22:08:18Z</dc:date>
    <item>
      <title>Synthesis and biological activities of new 7-&lt;i style=""&gt;o&lt;/i&gt;-&lt;img src='/image/spc_char/beta.gif' border=0&gt;-D-glucopyranosyloxy-3-(3-oxo-3-arylprop-1-enyl)-chromones</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/6515</link>
      <description>Title: Synthesis and biological activities of new 7-&lt;i style=""&gt;o&lt;/i&gt;-&lt;img src='/image/spc_char/beta.gif' border=0&gt;-D-glucopyranosyloxy-3-(3-oxo-3-arylprop-1-enyl)-chromones
Authors: Hatzade, K M; Taile, V S; Gaidhane, P K; Umare, V D; Haldar, A G M; Ingle, V N
Abstract: A convenient route to synthesize some new medicinally important 7-hydroxy-3-(3-oxo-3-arylprop-1-enyl)-chromones&lt;b style=""&gt; 2&lt;/b&gt; is described by the  interaction of 7-hydroxy-3-formyl chromone &lt;b style=""&gt;1&lt;/b&gt; with various substituted acetophenones which on condensation with 2,3,4,6-tetra-&lt;i style=""&gt;o&lt;/i&gt;-acetyl-&lt;img src='/image/spc_char/alpha.gif' border=0&gt;-D-glucopyranosyl bromide affords 2,3,4,6-tetra-&lt;i style=""&gt;o&lt;/i&gt;-acetyl-&lt;img src='/image/spc_char/beta.gif' border=0&gt;-D-glucopyranosyloxy-3-(3-oxo-3-arylprop-1-enyl)-4&lt;i style=""&gt;H&lt;/i&gt;-chromen-4-ones &lt;b style=""&gt;3&lt;/b&gt;. Later on deacetylation with anhydrous zinc acetate in methanol gives 7-&lt;i style=""&gt;o&lt;/i&gt;-&lt;img src='/image/spc_char/beta.gif' border=0&gt;-D-glucopyranosyloxy-3-(3-oxo-3-arylprop-1-enyl)-4&lt;i style=""&gt;H&lt;/i&gt;-chromen-4-ones &lt;b style=""&gt;4&lt;/b&gt;. These compounds are evaluated for their &lt;i style=""&gt;in vitro&lt;/i&gt; antimicrobial and antioxidant activity. The structures of these newly synthesized compounds are established by IR, NMR, mass spectra, elemental analysis and chemical analysis.
Page(s): 1548-1557</description>
      <pubDate>Sun, 01 Nov 2009 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/6515</guid>
      <dc:date>2009-11-01T00:00:00Z</dc:date>
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    <item>
      <title>Novel fluorescence emissions from 3-styrylindoles</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/6514</link>
      <description>Title: Novel fluorescence emissions from 3-styrylindoles
Authors: Singh, Anil K; Asefa, Abera
Abstract: &lt;smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="metricconverter"&gt; Fluorescence spectral properties of variously substituted 3-styrylindoles &lt;i&gt;viz.&lt;/i&gt; 3-(2-phenylethenyl-&lt;i style=""&gt;E&lt;/i&gt;)-NH-indole &lt;b style=""&gt;1&lt;/b&gt;, 3-[2-(4-ni­tro­phenyl)­ethenyl-&lt;i style=""&gt;E&lt;/i&gt;]-NH-indole &lt;b style=""&gt;2&lt;/b&gt;, 5-methoxy-3-[2-(4-nitro­phe­nyl)­ethenyl-&lt;i style=""&gt;E&lt;/i&gt;]-NH-indole &lt;b style=""&gt;3&lt;/b&gt;,3-[2-(4-chlorophenyl)ethenyl-&lt;i style=""&gt;E&lt;/i&gt;]-NH-indole &lt;b style=""&gt;4&lt;/b&gt; and 5-methoxy-3-[2-(4-chlorophenyl)ethenyl-&lt;i style=""&gt;E&lt;/i&gt;]-NH-indole &lt;b style=""&gt;5&lt;/b&gt; in solution and solid-state are described. &lt;/smarttagtype&gt;
Page(s): 1543-1547</description>
      <pubDate>Sun, 01 Nov 2009 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/6514</guid>
      <dc:date>2009-11-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Synthesis of quinoxaline quinones and regioselectivity in their Diels-Alder cycloadditions</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/6513</link>
      <description>Title: Synthesis of quinoxaline quinones and regioselectivity in their Diels-Alder cycloadditions
Authors: Sharma, Gitanjali; Raisinghani, Pankaj; Abraham, Ignatious; Pardasani, R T; Mukherjee, Tulsi
Abstract: A facile synthesis of quinoxaline quinones is reported. The regioselectivity in their Diels-Alder cycloaddition reactions has been investigated at AM1 level using Gaussian 98 and MOPAC 6 programs. The products have been characterized from their spectral data.
Page(s): 1590-1596</description>
      <pubDate>Sun, 01 Nov 2009 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/6513</guid>
      <dc:date>2009-11-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Microwave assisted synthesis and antimicrobial activity of some 2-(benzo­- furan-2-yl) -7-(substituted)imidazo[2,1-&lt;i style=""&gt;b&lt;/i&gt;]benzothiazoles</title>
      <link>http://nopr.niscpr.res.in/handle/123456789/6512</link>
      <description>Title: Microwave assisted synthesis and antimicrobial activity of some 2-(benzo­- furan-2-yl) -7-(substituted)imidazo[2,1-&lt;i style=""&gt;b&lt;/i&gt;]benzothiazoles
Authors: Rani, Rekha; Makrandi, J K
Abstract: 2-(Benzofuran-2-yl)-7-(substituted)imidazo[2,1-&lt;i style=""&gt;b&lt;/i&gt;]benzothia­z­oles have been prepared by condensation of 2-(2-bromoacetyl)­benzofurans and various 2-amino-7-(substituted) benzothiazoles under normal thermal condition as well as microwave irradiations. The latter condition for the reaction has been found to be much more efficient in terms of time and yield. The structures of the compounds have been established on the basis of their elemental analysis, IR and &lt;sup&gt;1&lt;/sup&gt;H NMR spectral data. The antibacterial and antifungal properties of these compounds are described.
Page(s): 1614-1617</description>
      <pubDate>Sun, 01 Nov 2009 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://nopr.niscpr.res.in/handle/123456789/6512</guid>
      <dc:date>2009-11-01T00:00:00Z</dc:date>
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