<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/15724" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/15724</id>
  <updated>2026-10-09T18:46:32Z</updated>
  <dc:date>2026-10-09T18:46:32Z</dc:date>
  <entry>
    <title>&lt;i&gt;Ab initio &lt;/i&gt;and MNDO study of structural parameters and pyramidal phosphorus &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;atom inversion in 1-substituted phosphorinanes&lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/16478" />
    <author>
      <name>Azizian, Javad</name>
    </author>
    <author>
      <name>Jadidi, Khosrow</name>
    </author>
    <author>
      <name>Mehrdad, Morteza</name>
    </author>
    <author>
      <name>Sarrafi, Yaghob</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/16478</id>
    <updated>2016-07-20T05:23:44Z</updated>
    <published>1999-06-01T00:00:00Z</published>
    <summary type="text">Title: &lt;i&gt;Ab initio &lt;/i&gt;and MNDO study of structural parameters and pyramidal phosphorus &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;atom inversion in 1-substituted phosphorinanes&lt;/span&gt;
Authors: Azizian, Javad; Jadidi, Khosrow; Mehrdad, Morteza; Sarrafi, Yaghob
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;A detailed &lt;i&gt;ab&#xD;
initio &lt;/i&gt;and MNDO study of structural parameters and pyramidal phosphorus&#xD;
atom inversion and also enthalpy differences &lt;span style="mso-bidi-font-style:&#xD;
italic"&gt;(∆&lt;i&gt;H&lt;/i&gt;&lt;sup&gt;o&lt;/sup&gt;)&lt;i&gt; &lt;/i&gt;between the participants in the&#xD;
conformational equilibrium...&lt;/span&gt;&lt;/span&gt;
Page(s): 660-663</summary>
    <dc:date>1999-06-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <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;Glucopyranosyl derivatives of 4-aminoquinoline and 2-methylimidazo[1,2-&lt;i style="mso-bidi-font-style: normal"&gt;α&lt;/i&gt;]-pyridine as potent reversible proton pump inhibitors&lt;sup&gt;†&lt;/sup&gt;&lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/16477" />
    <author>
      <name>Lohray, B B</name>
    </author>
    <author>
      <name>Bhushan, Vidya</name>
    </author>
    <author>
      <name>Reddy, A Sekar</name>
    </author>
    <author>
      <name>Lakshminarayana, N</name>
    </author>
    <author>
      <name>Rao, V Venugopal</name>
    </author>
    <author>
      <name>Saibaba, V</name>
    </author>
    <author>
      <name>Reddy, N Jaipal</name>
    </author>
    <author>
      <name>Kumar, Prem</name>
    </author>
    <author>
      <name>Reddy, K Narayan</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/16477</id>
    <updated>2016-07-20T05:28:13Z</updated>
    <published>1999-06-01T00:00:00Z</published>
    <summary type="text">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;Glucopyranosyl derivatives of 4-aminoquinoline and 2-methylimidazo[1,2-&lt;i style="mso-bidi-font-style: normal"&gt;α&lt;/i&gt;]-pyridine as potent reversible proton pump inhibitors&lt;sup&gt;†&lt;/sup&gt;&lt;/span&gt;
Authors: Lohray, B B; Bhushan, Vidya; Reddy, A Sekar; Lakshminarayana, N; Rao, V Venugopal; Saibaba, V; Reddy, N Jaipal; Kumar, Prem; Reddy, K Narayan
Abstract: Amongst a number of 4-aminoquinoline and 2-methylimidazo[1&lt;i&gt;,2,-a&lt;/i&gt;&lt;span style="mso-bidi-font-style:italic"&gt;]-pyridine&#xD;
&#xD;
&lt;span style="font-size:12.0pt;font-family:" 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;derivatives examined&#xD;
2-[3-butyryl-4-(2-methylphenylamino)quinoline-8-yloxy]ethyl  2,3,4,6-tetra-&lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;O&lt;/i&gt;-acetyl&lt;span style="font-size:12.0pt;font-family:&#xD;
" 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;-β-D-gluco&lt;span style="font-size:12.0pt;font-family:" 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;pyranoside and 3-ethoxycarbonyl-2-methylimidazo[1,2-&lt;i style="mso-bidi-font-style:normal"&gt;α&lt;/i&gt;]pyridine-8-yl &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;2,3,4,6-tetra-&lt;i style="mso-bidi-font-style:normal"&gt;O&lt;/i&gt;-acetyl-β-D-glucopyranoside&#xD;
&lt;span style="font-size:12.0pt;font-family:" 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;have been found to be good reversible proton&#xD;
pump inhibitors.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 635-638</summary>
    <dc:date>1999-06-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>&lt;span style="font-size:19.5pt;mso-bidi-font-size:14.5pt; 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;Studies on the Himalayan yew &lt;i&gt;Taxus wallichiana: &lt;/i&gt;Part VII - The taxoids and phenolic constituents of the roots of &lt;i&gt;Taxus wallichiana&lt;/i&gt;&lt;sup&gt;&lt;span style="mso-bidi-font-style:italic"&gt;†&lt;/span&gt;&lt;/sup&gt;&lt;i&gt; &lt;/i&gt;&lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/16476" />
    <author>
      <name>Chattopadhyay, S K</name>
    </author>
    <author>
      <name>Kulshrestha, M</name>
    </author>
    <author>
      <name>Tripathi, V</name>
    </author>
    <author>
      <name>Saha, G C</name>
    </author>
    <author>
      <name>Sharma, R P</name>
    </author>
    <author>
      <name>Mehta, V K</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/16476</id>
    <updated>2016-07-20T05:36:52Z</updated>
    <published>1999-06-01T00:00:00Z</published>
    <summary type="text">Title: &lt;span style="font-size:19.5pt;mso-bidi-font-size:14.5pt; 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;Studies on the Himalayan yew &lt;i&gt;Taxus wallichiana: &lt;/i&gt;Part VII - The taxoids and phenolic constituents of the roots of &lt;i&gt;Taxus wallichiana&lt;/i&gt;&lt;sup&gt;&lt;span style="mso-bidi-font-style:italic"&gt;†&lt;/span&gt;&lt;/sup&gt;&lt;i&gt; &lt;/i&gt;&lt;/span&gt;
Authors: Chattopadhyay, S K; Kulshrestha, M; Tripathi, V; Saha, G C; Sharma, R P; Mehta, V K
Abstract: &lt;span style="font-size:13.5pt;mso-bidi-font-size:8.5pt"&gt;The systematic investigation&#xD;
on the roots of &lt;i&gt;Taxus wallichiana &lt;/i&gt;has resulted in the isolation of nine&#xD;
taxoids-taxol &lt;b style="mso-bidi-font-weight:normal"&gt;1 &lt;/b&gt;baccatin III &lt;b style="mso-bidi-font-weight:normal"&gt;2&lt;/b&gt;, baccatin IV &lt;b style="mso-bidi-font-weight:&#xD;
normal"&gt;3&lt;/b&gt;, taxusin &lt;b style="mso-bidi-font-weight:normal"&gt;4&lt;/b&gt;, a C-14&#xD;
oxygenated taxoid &lt;b style="mso-bidi-font-weight:normal"&gt;5&lt;/b&gt;, 1β&lt;span style="font-size:11.5pt;mso-bidi-font-size:6.5pt;font-family:HiddenHorzOCR;&#xD;
mso-bidi-font-family:HiddenHorzOCR"&gt;-hydroxybaccatin &lt;b style="mso-bidi-font-weight:&#xD;
normal"&gt;I &lt;/b&gt;&lt;b style="mso-bidi-font-weight:normal"&gt;&lt;span style="font-size:13.5pt;mso-bidi-font-size:8.5pt"&gt;6&lt;/span&gt;&lt;/b&gt;&lt;span style="font-size:13.5pt;mso-bidi-font-size:8.5pt"&gt;, pentaacetoxy taxadiene &lt;b style="mso-bidi-font-weight:normal"&gt;7&lt;/b&gt;, a&#xD;
&#xD;
&lt;span style="font-size:13.5pt;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;dibenzoylated rearranged taxoid &lt;b style="mso-bidi-font-weight:normal"&gt;8&lt;/b&gt;, 7-xylosyl-10-deacetyl-taxol C &lt;b style="mso-bidi-font-weight:normal"&gt;9&lt;/b&gt; and three phenolic compounds (-)&#xD;
seco-isolariciresinol &lt;b style="mso-bidi-font-weight:normal"&gt;11&lt;/b&gt;,&#xD;
taxiresinol &lt;b style="mso-bidi-font-weight:normal"&gt;12&lt;/b&gt; and isotaxiresinol &lt;b style="mso-bidi-font-weight:normal"&gt;13&lt;/b&gt;. The compounds have been&#xD;
characterized on the basis of their spectral characteristics. The occurrence of&#xD;
taxoid &lt;b style="mso-bidi-font-weight:normal"&gt;9&lt;/b&gt; in the roots of the plant&#xD;
is quite significant. The distribution of the above compounds in other parts of&#xD;
the plant are also summarized.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 701-704</summary>
    <dc:date>1999-06-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <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;Synthesis and reactions of some new 5-aryl-3-oxo-7 -(4'-aryl-2' ,5 '-dioxo-1', 2' ,3 ', 4'-tetrahydrofluoren-3'-yl)-5&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;, 8&lt;i&gt;H-&lt;/i&gt;&lt;span style="mso-bidi-font-style: italic"&gt;2,3&lt;i&gt;- &lt;/i&gt;dihydrothiazolo[5&lt;i&gt;,&lt;/i&gt;&lt;span style="mso-bidi-font-style: italic"&gt;4-&lt;i&gt;b&lt;/i&gt;]pyrimidines of expected biological activity&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/16475" />
    <author>
      <name>Salama, M A</name>
    </author>
    <author>
      <name>EI-Essa, S A</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/16475</id>
    <updated>2016-07-20T05:46:14Z</updated>
    <published>1999-06-01T00:00:00Z</published>
    <summary type="text">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;Synthesis and reactions of some new 5-aryl-3-oxo-7 -(4'-aryl-2' ,5 '-dioxo-1', 2' ,3 ', 4'-tetrahydrofluoren-3'-yl)-5&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;, 8&lt;i&gt;H-&lt;/i&gt;&lt;span style="mso-bidi-font-style: italic"&gt;2,3&lt;i&gt;- &lt;/i&gt;dihydrothiazolo[5&lt;i&gt;,&lt;/i&gt;&lt;span style="mso-bidi-font-style: italic"&gt;4-&lt;i&gt;b&lt;/i&gt;]pyrimidines of expected biological activity&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Authors: Salama, M A; EI-Essa, S A
Abstract: 2-Arylidene-indane-1,3-dione &lt;b style="mso-bidi-font-weight:normal"&gt;1&lt;/b&gt;&#xD;
on treatment with acetyl acetone in gl. acetic acid gives 3-acetyl-4-aryl-2,5-dioxo-1,2,3,4-&#xD;
tetrahydrofluorenes &lt;b style="mso-bidi-font-weight:normal"&gt;2a-d&lt;/b&gt; which on&#xD;
reaction with benzaldehyde yield 4-aryl-3-cinnamoyl-2, 5-dioxo-1, 2, 3,&#xD;
4-tetrahydrofluorenes&#xD;
&#xD;
&lt;b style="mso-bidi-font-weight:normal"&gt;3a-d&lt;/b&gt;. Compounds &lt;b style="mso-bidi-font-weight:normal"&gt;3a-d&lt;/b&gt; when&#xD;
reacted with thiourea in gl. CH&lt;sub&gt;3&lt;/sub&gt;COOH/Ac&lt;sub&gt;2&lt;/sub&gt;O in the presence&#xD;
of anhyd. sodium acetate afford 4,5-diaryl-6-(4'-aryl-2', &lt;span style="mso-bidi-font-style:italic"&gt;5&lt;i&gt;' &lt;/i&gt;-dioxo-1', 2', 3', 4'-tetrahydrofluoren-&#xD;
3'-yl)-1, 2, 3, 4-tetrahydropyrimidine-2-thiones &lt;b style="mso-bidi-font-weight:&#xD;
normal"&gt;4a-d&lt;/b&gt; which on&#xD;
&#xD;
&lt;span style="font-size:12.0pt;font-family:" 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;treatment with chloroacetic acid furnish 5-aryl-3-oxo-7-(4'-aryl-&#xD;
&lt;span style="mso-bidi-font-style:italic"&gt;2'&lt;i&gt;, &lt;/i&gt;5' -dioxo-1',2',3',4'&#xD;
-tetrahydrofluoren-3'-yl)-5&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;, &lt;span style="mso-bidi-font-style:italic"&gt;8&lt;i&gt;H-&lt;/i&gt;2,3-dihydrothi azolo[5,4-b]pyrimidines&#xD;
&lt;b style="mso-bidi-font-weight:normal"&gt;5a-d&lt;/b&gt;. Compounds &lt;b style="mso-bidi-font-weight:&#xD;
normal"&gt;5a-d&lt;/b&gt; on condensation with benzaldehyde yield&#xD;
2-arylmethylene-3-oxo-Sphenyl-7-(4' -aryl-2', 5' -dioxo-1',  2', 3', 4'-tetrahydrotluoren-3'&lt;i&gt;yl)-&lt;/i&gt;&lt;span style="mso-bidi-font-style:italic"&gt;5&lt;i&gt;H, &lt;/i&gt;8&lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;H&lt;/i&gt;-2,3-dihydrothiazolo[5,4- &lt;i&gt;b &lt;/i&gt;]pyrimidines &lt;b style="mso-bidi-font-weight:normal"&gt;6a-d&lt;/b&gt;.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 739-742</summary>
    <dc:date>1999-06-01T00:00:00Z</dc:date>
  </entry>
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