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  <channel rdf:about="http://nopr.niscpr.res.in/handle/123456789/15726">
    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/15726</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/16595" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/16594" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/16593" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/16592" />
      </rdf:Seq>
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    <dc:date>2026-10-09T09:40:41Z</dc:date>
  </channel>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/16595">
    <title>A new method for dehydrogenation of symmetric hydrazo compound</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/16595</link>
    <description>Title: A new method for dehydrogenation of symmetric hydrazo compound
Authors: Wang, Cailan; Wang, Xiaoxia; Wang, Yulu
Abstract: A new synthetic route with N-bromosuccinimide (NBS) and pyridine as&#xD;
oxidation system to dehydrogenate symmetric hydrazo compounds for preparing azo&#xD;
compounds is reported for the first time. Eight azo compounds are prepared in&#xD;
good yields under mild conditions and possible mechanism has been suggested.
Page(s): 964-965</description>
    <dc:date>1999-08-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/16594">
    <title>&lt;span style="font-size:12.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-ansi-language: EN-IN;mso-fareast-language:EN-IN;mso-bidi-language:AR-SA" lang="EN-IN"&gt;New pterocarpans from &lt;i&gt;Oroxylum indicum &lt;/i&gt;stem bark&lt;/span&gt;</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/16594</link>
    <description>Title: &lt;span style="font-size:12.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-ansi-language: EN-IN;mso-fareast-language:EN-IN;mso-bidi-language:AR-SA" lang="EN-IN"&gt;New pterocarpans from &lt;i&gt;Oroxylum indicum &lt;/i&gt;stem bark&lt;/span&gt;
Authors: Ali, Mohd; Chaudhary, Anurag; Ramachandram, Ramidi
Abstract: From the stem bark of &lt;i&gt;Oroxylum &lt;/i&gt;four new pterocarpans, namely&#xD;
methyl oroxylopterocarpan &lt;b style="mso-bidi-font-weight:normal"&gt;1&lt;/b&gt;, undecanyl&#xD;
oroxylopterocarpan &lt;b style="mso-bidi-font-weight:normal"&gt;2&lt;/b&gt;, hexyl&#xD;
oroxylopterocarpan &lt;b style="mso-bidi-font-weight:normal"&gt;3&lt;/b&gt;, and heptyl&#xD;
oroxylopterocarpan &lt;b style="mso-bidi-font-weight:normal"&gt;4&lt;/b&gt;, have been&#xD;
isolated and characterized as&#xD;
&#xD;
2', 3'-dihydro-2',2'-dimethyl-2,3-furanylpterocarpan; 2',3'-dihydro-2'-methyl-2'-undecanyl-2,3-furanyl-8-hydroxypterocarpan;&#xD;
2',3'dihydro-2'-methyl-2'-undercanyl-2,3-furanyl-8-hydroxypterocarpan and&#xD;
2',3'- dihydro-2'- hexyl-2,3-furanyl-8- hydroxypterocarpan on the basis of&#xD;
spectral data and chemical analysis.
Page(s): 950-952</description>
    <dc:date>1999-08-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/16593">
    <title>Revised structures of the flavonoids from &lt;i&gt;Limnophila gratissima &lt;/i&gt;(Scrophulariaceae)</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/16593</link>
    <description>Title: Revised structures of the flavonoids from &lt;i&gt;Limnophila gratissima &lt;/i&gt;(Scrophulariaceae)
Authors: Krishnan, Sujatha; Nair, A G Ramachandran
Abstract: &lt;span style="font-size:12.0pt;font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-ansi-language:="" en-in;mso-fareast-language:en-in;mso-bidi-language:ar-sa"="" lang="EN-IN"&gt;7-Desmethylartemetin&#xD;
(5,7-dihydroxy-3,6,3',4'-tetramethoxy-flavone), a rare flavonoid reported from &lt;i&gt;Limnophila&#xD;
gratissima, &lt;/i&gt;has been found to be a mixture or two) flavones [5,7-dihydroxy-&#xD;
6,8,4'-trimethoxyflavone (nevadensin) and 5-hydroxy-6,7.4'-trimethoxy flavone &lt;span style="font-size:12.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:="" hiddenhorzocr;mso-ansi-language:en-in;mso-fareast-language:en-in;mso-bidi-language:="" ar-sa"="" lang="EN-IN"&gt;(salvigenin)]&lt;span style="font-size:12.0pt;font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-ansi-language:="" en-in;mso-fareast-language:en-in;mso-bidi-language:ar-sa"="" lang="EN-IN"&gt;. Besides the plant&#xD;
contains two phenolic acids; caffeic acid and chlorogenic acid. The present finding&#xD;
is supported by  chemotaxonomy of&#xD;
Scrophulariaceae.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 1009-1010</description>
    <dc:date>1999-08-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/16592">
    <title>&lt;span style="font-size:18.0pt;mso-bidi-font-size:14.0pt;mso-ansi-language:EN-US; mso-fareast-language:EN-US"&gt;X-Ray crystallographic study of &lt;span style="font-size:18.0pt;mso-bidi-font-size:14.0pt;mso-ansi-language:EN-US; mso-fareast-language:EN-US"&gt;1-methyl-4-( 4-&lt;i style="mso-bidi-font-style:normal"&gt;N,N&lt;/i&gt;-dimethylamino) &lt;span style="font-size:18.0pt;mso-bidi-font-size:14.0pt;font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";mso-ansi-language:EN-US;mso-fareast-language: EN-US;mso-bidi-language:AR-SA"&gt;styryl pyridinium iodide&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/16592</link>
    <description>Title: &lt;span style="font-size:18.0pt;mso-bidi-font-size:14.0pt;mso-ansi-language:EN-US; mso-fareast-language:EN-US"&gt;X-Ray crystallographic study of &lt;span style="font-size:18.0pt;mso-bidi-font-size:14.0pt;mso-ansi-language:EN-US; mso-fareast-language:EN-US"&gt;1-methyl-4-( 4-&lt;i style="mso-bidi-font-style:normal"&gt;N,N&lt;/i&gt;-dimethylamino) &lt;span style="font-size:18.0pt;mso-bidi-font-size:14.0pt;font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";mso-ansi-language:EN-US;mso-fareast-language: EN-US;mso-bidi-language:AR-SA"&gt;styryl pyridinium iodide&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Authors: Mishra, A; Behera, R K; Fronczek, F R; Vidyasagar, M; Behera, G B
Abstract: &lt;span style="font-size:13.0pt;mso-bidi-font-size:9.0pt;mso-ansi-language:EN-US;&#xD;
mso-fareast-language:EN-US"&gt;Styryl pyridinium iodide dye (C&lt;sub&gt;16&lt;/sub&gt;H&lt;sub&gt;19&lt;/sub&gt;N&lt;sub&gt;2&lt;/sub&gt;I), is monoclinic &lt;i&gt;P&lt;/i&gt;2&lt;sub&gt;1&lt;/sub&gt;/c&lt;i&gt;,&lt;/i&gt;&#xD;
&#xD;
a= 6.3313(8)Å, b= 7699(2) Å, c=32.119(7) Å, &lt;i style="mso-bidi-font-style:normal"&gt;β&lt;/i&gt;= 90.39(1)° &lt;i&gt;,V&lt;/i&gt;=&#xD;
&#xD;
1565.6(9) Å&lt;sup&gt;3&lt;/sup&gt;, Z= 4, D&lt;sub&gt;c&lt;/sub&gt;= 1.544gcm&lt;sup&gt;-3&lt;/sup&gt;,&#xD;
λ(MoK&lt;img src='/image/spc_char/alpha.gif' border=0&gt;)= 0.7 1073 Å, μ&lt;i&gt;=&lt;/i&gt;&#xD;
&#xD;
&lt;span style="font-size:13.0pt;mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman";="" mso-fareast-font-family:"times="" roman";mso-ansi-language:en-us;mso-fareast-language:="" en-us;mso-bidi-language:ar-sa"=""&gt;20.12cm&lt;sup&gt;-1&lt;/sup&gt; , &lt;i style="mso-bidi-font-style:normal"&gt;&lt;span style="font-size:9.0pt;mso-bidi-font-size:&#xD;
5.0pt;font-family:Arial;mso-fareast-font-family:" times="" new="" roman";mso-ansi-language:="" en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;F&lt;/span&gt;&lt;/i&gt;&lt;sub&gt;&lt;span style="font-size:9.0pt;mso-bidi-font-size:5.0pt;font-family:Arial;mso-fareast-font-family:&#xD;
" times="" new="" roman";mso-ansi-language:en-us;mso-fareast-language:en-us;="" mso-bidi-language:ar-sa"=""&gt;000&lt;/span&gt;&lt;/sub&gt;&lt;span style="font-size:9.0pt;&#xD;
mso-bidi-font-size:5.0pt;font-family:Arial;mso-fareast-font-family:" times="" new="" roman";="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt; &lt;span style="font-size:13.0pt;mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman";="" mso-fareast-font-family:"times="" roman";mso-ansi-language:en-us;mso-fareast-language:="" en-us;mso-bidi-language:ar-sa"=""&gt;= 728, T = 298 °K. 4707 unique reflections &lt;span style="font-size:10.5pt;mso-bidi-font-size:6.5pt;font-family:HiddenHorzOCR;&#xD;
mso-hansi-font-family:" times="" new="" roman";mso-bidi-font-family:hiddenhorzocr;="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;measured;&#xD;
&lt;span style="font-size:13.0pt;mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman";="" mso-fareast-font-family:"times="" roman";mso-ansi-language:en-us;mso-fareast-language:="" en-us;mso-bidi-language:ar-sa"=""&gt;final R=0.032 for 3959 retlections with &lt;i style="mso-bidi-font-style:normal"&gt;&lt;span style="font-size:12.5pt;mso-bidi-font-size:&#xD;
8.5pt;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" mso-ansi-language:en-us;mso-fareast-language:en-us;mso-bidi-language:ar-sa"=""&gt;I&lt;/span&gt;&lt;/i&gt;&lt;span style="font-size:12.5pt;mso-bidi-font-size:8.5pt;font-family:" times="" new="" roman";="" mso-fareast-font-family:"times="" roman";mso-ansi-language:en-us;mso-fareast-language:="" en-us;mso-bidi-language:ar-sa"=""&gt; &gt; 1&lt;span style="font-size:13.0pt;&#xD;
mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:="" "times="" roman";mso-ansi-language:en-us;mso-fareast-language:en-us;="" mso-bidi-language:ar-sa"=""&gt;.0σ(&lt;i style="mso-bidi-font-style:normal"&gt;I&lt;/i&gt;). The three&#xD;
dimensional structure of the dye is presented. The structure analysis shows&#xD;
that the dye exist in trans form and is approximately planner.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 982-985</description>
    <dc:date>1999-08-01T00:00:00Z</dc:date>
  </item>
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