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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.49B(12) December 2010]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10730</link>
    <description />
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/10740">
    <title>High atom efficient and environment-friendly preparation of herbicides bromoxynil and ioxynil</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10740</link>
    <description>Title: High atom efficient and environment-friendly preparation of herbicides bromoxynil and ioxynil
&lt;br/&gt;
&lt;br/&gt;Authors: Subbarayappa, dimurthy; Joshi, Girdhar; Patil, Rajendra D
&lt;br/&gt;
&lt;br/&gt;Abstract: High atom efficient and&#xD;
environment-friendly preparation of herbicides bromoxynil and ioxynil using&#xD;
bromide/bromate and iodide/iodate couple as halogenating reagent in water at room&#xD;
temperature is described.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1678-1680</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/10739">
    <title>Studies of antimicrobial activity of picryl amino pyridine N-oxides</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10739</link>
    <description>Title: Studies of antimicrobial activity of picryl amino pyridine N-oxides
&lt;br/&gt;
&lt;br/&gt;Authors: Badgujar, D M; Talawar, M B; Asthana, S N; Mahulikar, P P
&lt;br/&gt;
&lt;br/&gt;Abstract: Biologically active picryl&#xD;
amino pyridines and their N-oxide have been successfully synthesized and&#xD;
screened for their antimicrobial potency to set-up the structure activity&#xD;
relationships and found to possess better antibacterial activity than&#xD;
antifungal activity.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1675-1677</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/10738">
    <title>Synthesis and bioactivity evaluation of pyrazolone derivatives</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10738</link>
    <description>Title: Synthesis and bioactivity evaluation of pyrazolone derivatives
&lt;br/&gt;
&lt;br/&gt;Authors: Mariappan, G; Saha, B P; Sutharson, L; Haldar, A
&lt;br/&gt;
&lt;br/&gt;Abstract: 3-Methyl-4-substituted&#xD;
benzylidene-pyrazol-5-ones &lt;b style=""&gt;1-10&lt;/b&gt; are&lt;b style=""&gt; &lt;/b&gt;synthesized by the condensation of&#xD;
3-methyl-pyrazol-5-one with substituted aliphatic and aromatic aldehydes. Their&#xD;
structures have been elucidated from UV-Vis, IR, &lt;sup&gt;1&lt;/sup&gt;H NMR and mass&#xD;
spectral data. Among the synthesized derivatives &lt;b style=""&gt;5, 6, 7&lt;/b&gt; and &lt;b style=""&gt;10&lt;/b&gt; are found&#xD;
to have a potent anti-inflammatory response whereas compounds &lt;b style=""&gt;1, 4, 5, 8&lt;/b&gt; and &lt;b style=""&gt;10&lt;/b&gt; have an effective analgesic response. There is no remarkable difference in bioactivity of pyrazolones derived&#xD;
from aliphatic and aromatic aldehydes. All the experimental data are&#xD;
statistically significant at p&lt;0.05.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1671-1674</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/10737">
    <title>Synthesis of &lt;i style=""&gt;N-&lt;/i&gt;1-(3,5-dimethyl-4-isoxozolyl)-3-(4-aryl-5-thioxo-4,5-dihydro-1-&lt;i style=""&gt;H&lt;/i&gt;–1, 2, 4-triazol–3-yl)propanamides as possible antitumor agents</title>
    <link>http://nopr.niscair.res.in/handle/123456789/10737</link>
    <description>Title: Synthesis of &lt;i style=""&gt;N-&lt;/i&gt;1-(3,5-dimethyl-4-isoxozolyl)-3-(4-aryl-5-thioxo-4,5-dihydro-1-&lt;i style=""&gt;H&lt;/i&gt;–1, 2, 4-triazol–3-yl)propanamides as possible antitumor agents
&lt;br/&gt;
&lt;br/&gt;Authors: Reddy, Ch V Narsimha; Raju, S; Reddy, M Nagi; Rajanarendar, E
&lt;br/&gt;
&lt;br/&gt;Abstract: Synthesis of &lt;i style=""&gt;N&lt;/i&gt;-1 (3,&#xD;
5-dimethyl-4-isoxazolyl)-3-(4-aryl-5-thioxo-4,5-dihydro-1&lt;i style=""&gt;H&lt;/i&gt;-1,2,4-triazol-3-yl)-propanamides &lt;b style=""&gt;7 &lt;/b&gt;have been accomplished from 4-amino-3,5-dimethylisoxazole &lt;b style=""&gt;1&lt;/b&gt; in&#xD;
five steps. The structural elucidation of the synthesized compounds has been&#xD;
performed by IR, &lt;sup&gt;1&lt;/sup&gt;H NMR and mass spectroscopic data besides&#xD;
elemental analyses.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1667-1670</description>
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