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    <title>NOPR Collection:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/21477</link>
    <description />
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        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/21668" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/21667" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/21666" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/21665" />
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    <dc:date>2026-10-09T12:04:01Z</dc:date>
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  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/21668">
    <title>Components from whole plant of &lt;i&gt;Phyllanthus amarus &lt;/i&gt;Linn</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/21668</link>
    <description>Title: Components from whole plant of &lt;i&gt;Phyllanthus amarus &lt;/i&gt;Linn
Authors: Ahmad, Bahar; Alam, Tanveer
Abstract: The whole plant of &lt;i&gt;Phyllanthus amarus &lt;/i&gt;Linn.&#xD;
has afforded new &lt;i&gt;seco&lt;/i&gt;sterols&lt;i&gt; &lt;/i&gt;named as amarosterol-A characterized&#xD;
as 13,14-&lt;i&gt;seco&lt;/i&gt;-stigma 5(6), 14(15)-diene-3-α-ol &lt;b&gt;1&lt;/b&gt;, and amarosterol-B&#xD;
characterized as 13 ,14-&lt;i&gt;seco-stigma &lt;/i&gt;9(11), 14(15)-diene-3-α-ol &lt;b&gt;2&lt;/b&gt;.&#xD;
&#xD;
Their structures have been elucidated on the&#xD;
basis of spectral and chemical studies.
Page(s): 1786-1790</description>
    <dc:date>2003-07-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/21667">
    <title>Terpenoid and lipid constituents from &lt;i&gt;Artemisia annua&lt;/i&gt;&lt;sup&gt;†&lt;/sup&gt;</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/21667</link>
    <description>Title: Terpenoid and lipid constituents from &lt;i&gt;Artemisia annua&lt;/i&gt;&lt;sup&gt;†&lt;/sup&gt;
Authors: Tewari, Amit; Bhakuni, Rajendra Singh
Abstract: Two new compounds, a bisnor cadinane 3α, 5β-dihydroxy-4α,11-epoxybisnor cadinane &lt;b&gt;1&lt;/b&gt; and the other lipid constituent methyl-11,&#xD;
12,15-trihydroxy-13(14)-octadecanoate &lt;b&gt;3&lt;/b&gt; have been&#xD;
&#xD;
isolated from the leaves of &lt;i&gt;Artemisia&#xD;
annua. &lt;/i&gt;Their structures have been established on the basis of their spectral&#xD;
and chemical studies.
Page(s): 1782-1785</description>
    <dc:date>2003-07-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/21666">
    <title>Synthesis and antibacterial activity of amoenylin, a metabolite of &lt;i&gt;Dendrobium&lt;/i&gt; &lt;i&gt;amoenum&lt;/i&gt;&lt;sup&gt;†&lt;/sup&gt;</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/21666</link>
    <description>Title: Synthesis and antibacterial activity of amoenylin, a metabolite of &lt;i&gt;Dendrobium&lt;/i&gt; &lt;i&gt;amoenum&lt;/i&gt;&lt;sup&gt;†&lt;/sup&gt;
Authors: Venkateswarlu, Somepalli; Ramachandra, Marellapudi S.; Subbaraju, Gottumukkala V
Abstract: Amoenylin &lt;b&gt;6&lt;/b&gt;, a dihydrostilbene from&#xD;
&lt;i&gt;Dendrobium amoenum &lt;/i&gt;has been synthesised from sy ringaldehyde &lt;b&gt;1&lt;/b&gt;, in&#xD;
three steps with an&lt;i&gt; &lt;/i&gt;overall yield of 40%. The spectral data of synthetic&#xD;
&lt;b&gt;6&lt;/b&gt; are in good&lt;i&gt; &lt;/i&gt;agreement with those of natural product. Amoenylin &lt;b&gt;6&lt;/b&gt;&#xD;
shows&lt;i&gt; &lt;/i&gt;weak antibacterial activity.
Page(s): 1779-1781</description>
    <dc:date>2003-07-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/21665">
    <title>A rapid and efficient method for acetylation of phenols with acetic anhydride catalysed by TiO&lt;sub&gt;2&lt;/sub&gt;/SO&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;2-&lt;/sup&gt; solid superacid</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/21665</link>
    <description>Title: A rapid and efficient method for acetylation of phenols with acetic anhydride catalysed by TiO&lt;sub&gt;2&lt;/sub&gt;/SO&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;2-&lt;/sup&gt; solid superacid
Authors: Ma, Yan-Ran; Jin, Tong-Shou; Wang, Zhen-Hua; Li, Tong-Shuang
Abstract: A rapid and efficient method for acetylation&#xD;
of phenols with acetic anhydride in the presence of TiO&lt;sub&gt;2&lt;/sub&gt;/SO&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;2-&lt;/sup&gt;&#xD;
solid superacid at room or at reflux temperature in excellent yield is described.
Page(s): 1777-1778</description>
    <dc:date>2003-07-01T00:00:00Z</dc:date>
  </item>
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