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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.48B(03) [March 2009]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/3361</link>
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    <title>The Collection's search engine</title>
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/3474">
    <title>Synthesis of (± )- (E)-2,6-dimethyl-6-hydroxy-2,7-octadienoic acid, its methyl ester and (± )- (E)-2,6-dimethyl-octa-2,7-diene-1,6-diol over solid support using microwave</title>
    <link>http://nopr.niscair.res.in/handle/123456789/3474</link>
    <description>Title: Synthesis of (± )- (E)-2,6-dimethyl-6-hydroxy-2,7-octadienoic acid, its methyl ester and (± )- (E)-2,6-dimethyl-octa-2,7-diene-1,6-diol over solid support using microwave
&lt;br/&gt;
&lt;br/&gt;Authors: Singh, Ashima; Sharma, M L; Singh, Jasvinder
&lt;br/&gt;
&lt;br/&gt;Abstract: A simple, exceedingly mild, ecofriendly and efficient methodology for the synthesis of (±)-(E)-2,6-dimethyl-6-hydroxy-2,7-octadienoic acid, its methyl ester and (±)-(E)-2,6-dimethyl-octa-2,7-diene-1,6-diol by utilization of microwave energy has been achieved.
&lt;br/&gt;
&lt;br/&gt;Page(s): 452-454</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/3473">
    <title>Synthesis of some new pyrazolines and isoxazoles carrying 4-methylthiophenyl moiety as potential analgesic and anti-inflammatory agents</title>
    <link>http://nopr.niscair.res.in/handle/123456789/3473</link>
    <description>Title: Synthesis of some new pyrazolines and isoxazoles carrying 4-methylthiophenyl moiety as potential analgesic and anti-inflammatory agents
&lt;br/&gt;
&lt;br/&gt;Authors: T, Karabasanagouda; Adhikari, Airody Vasudeva; M, Girisha
&lt;br/&gt;
&lt;br/&gt;Abstract: A series of new pyrazolines 3a-m and isoxazoles 4a-k have been synthesized from 4-acetylthioanisole, 1 with aryl aldehydes through α, β-unsaturated ketones. The structures of the newly synthesized compounds have been confirmed on the basis of elemental analysis and spectral studies. The newly synthesized title compounds have been tested for their analgesic and anti-inflammatory activity. Some of the compounds exhibited encouraging results
&lt;br/&gt;
&lt;br/&gt;Page(s): 430-437</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/3472">
    <title>Synthesis of dimethyl ether of marsupsin</title>
    <link>http://nopr.niscair.res.in/handle/123456789/3472</link>
    <description>Title: Synthesis of dimethyl ether of marsupsin
&lt;br/&gt;
&lt;br/&gt;Authors: Srikrishna, A; Mathews, M
&lt;br/&gt;
&lt;br/&gt;Abstract: Total synthesis of the dimethyl ether of marsupsin, in seven steps starting from phloroglucinol, is described.
&lt;br/&gt;
&lt;br/&gt;Page(s): 383-385</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/3471">
    <title>One pot stereoselective synthesis of isoxazolines from N-phenyl-α- chloro nitrone</title>
    <link>http://nopr.niscair.res.in/handle/123456789/3471</link>
    <description>Title: One pot stereoselective synthesis of isoxazolines from N-phenyl-α- chloro nitrone
&lt;br/&gt;
&lt;br/&gt;Authors: Chakraborty, Bhaskar; Kafley, Saurav; Chhetri, Manjit Singh
&lt;br/&gt;
&lt;br/&gt;Abstract: Isoxazolines have been synthesized from N-phenyl-α-chloro nitrone using 1,3 dipolar cycloaddition reaction with alkynes and the reactions are found to be highly stereoselective in nature. The products have been characterized by analytical and spectral (IR, ¹H NMR, ¹³C NMR and mass) data.
&lt;br/&gt;
&lt;br/&gt;Page(s): 447-451</description>
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