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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.51B(07) [July 2012]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/14323</link>
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      <title>&lt;span style="font-size:12.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-ansi-language: EN-GB;mso-fareast-language:EN-US;mso-bidi-language:AR-SA" lang="EN-GB"&gt;Potassium phosphate &lt;span style="mso-bidi-font-weight:bold"&gt;catalyzed efficient synthesis of 3-carboxycoumarins&lt;/span&gt;&lt;/span&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/14362</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-GB;mso-fareast-language:EN-US;mso-bidi-language:AR-SA" lang="EN-GB"&gt;Potassium phosphate &lt;span style="mso-bidi-font-weight:bold"&gt;catalyzed efficient synthesis of 3-carboxycoumarins&lt;/span&gt;&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Undale, Kedar A; Gaikwad, Dipak S; Shaikh, Tarannum S; Desai, Uday V; Pore, Dattaprasad M
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;span style="font-size:12.0pt;font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-ansi-language:="" en-gb;mso-fareast-language:en-us;mso-bidi-language:ar-sa"="" lang="EN-GB"&gt;An efficient and&#xD;
rapid synthesis of 3-carboxycoumarins&lt;b style="mso-bidi-font-weight:normal"&gt; &lt;/b&gt;has&#xD;
been expediently accomplished by a reaction of salicylaldehyde with Meldrum’s acid&#xD;
using potassium phosphate as an inexpensive catalyst at ambient temperature. &lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 1039-1042</description>
      <pubDate>Thu, 28 Jun 2012 22:58:59 GMT</pubDate>
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    <item>
      <title>&lt;span style="font-size:12.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-ansi-language: EN-GB;mso-fareast-language:EN-US;mso-bidi-language:AR-SA" lang="EN-GB"&gt;Fuller’s earth catalyzed rapid synthesis of bis(indolyl)methanes under solvent free condition&lt;/span&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/14361</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-GB;mso-fareast-language:EN-US;mso-bidi-language:AR-SA" lang="EN-GB"&gt;Fuller’s earth catalyzed rapid synthesis of bis(indolyl)methanes under solvent free condition&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Kapuriya, Naval; Kakadiya, Rajesh; Savant, Mahesh M; Pansuriya, Akshay M; Bhuva, Chirag V; Patel, Anil S; Pipaliya, Piyush V; Audichya, Vipul B; Gangadharaiah, Sarala; Anandalwar, Sridhar M; Prasad, Javaregowda S; Shah, Anamik; Naliapara, Yogesh T
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;span style="font-size:12.0pt;font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-ansi-language:="" en-gb;mso-fareast-language:en-us;mso-bidi-language:ar-sa"="" lang="EN-GB"&gt;A rapid and highly&#xD;
efficient synthesis of various bis(indolyl)methanes with high yield by the reaction&#xD;
of indoles &lt;b style="mso-bidi-font-weight:normal"&gt;1a-c&lt;/b&gt; and arylaldehydes &lt;b style="mso-bidi-font-weight:normal"&gt;2a'-m'&lt;/b&gt; in presence of fuller’s earth is&#xD;
demonstrated. &lt;span style="font-size:12.0pt;font-family:" times="" new="" roman";="" mso-fareast-font-family:"times="" roman";mso-ansi-language:pl;mso-fareast-language:="" en-us;mso-bidi-language:ar-sa"="" lang="PL"&gt;This simple and versatile protocol is found to&#xD;
be an efficient catalyst for the electrophilic addition reaction of indole and&#xD;
works well under solvent free condition as well as in aqueous medium. The&#xD;
structure of newly synthesized compound &lt;b style="mso-bidi-font-weight:normal"&gt;3m&lt;/b&gt;&#xD;
has been confirmed by single crystal X-ray crystallography.&lt;/span&gt;&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 1032-1038</description>
      <pubDate>Thu, 28 Jun 2012 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>&lt;span style="font-size:12.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-ansi-language: EN-GB;mso-fareast-language:EN-US;mso-bidi-language:AR-SA" lang="EN-GB"&gt;Studies on the reaction of N-bromo­succinimide in dimethylsulphoxide: Part X — Action on cholest-4-en-3,6-dione&lt;/span&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/14360</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-GB;mso-fareast-language:EN-US;mso-bidi-language:AR-SA" lang="EN-GB"&gt;Studies on the reaction of N-bromo­succinimide in dimethylsulphoxide: Part X — Action on cholest-4-en-3,6-dione&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Pradhan, B P; Debnath, Utpal; Pradhan, Nagendra Narayan; Ghosh, Pranab
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;span style="font-size:12.0pt;font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-ansi-language:="" en-gb;mso-fareast-language:en-us;mso-bidi-language:ar-sa"="" lang="EN-GB"&gt;The reaction of&#xD;
cholest-4-en-3,6-dione, &lt;b&gt;1&lt;/b&gt; with N-bromo­succinimide in dimethyl&#xD;
sulphoxide furnishes three compounds which have been identified as 2,7&lt;span style="font-size:12.0pt;font-family:Symbol;mso-ascii-font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-hansi-font-family:="" "times="" roman";mso-bidi-font-family:"times="" roman";mso-ansi-language:="" en-gb;mso-fareast-language:en-us;mso-bidi-language:ar-sa;mso-char-type:symbol;="" mso-symbol-font-family:symbol"="" lang="EN-GB"&gt;a&lt;span style="font-size:12.0pt;font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-ansi-language:="" en-gb;mso-fareast-language:en-us;mso-bidi-language:ar-sa"="" lang="EN-GB"&gt;-dibromocholest-1,4-dien-3,6-dione&#xD;
&lt;b&gt;2&lt;/b&gt;, 2,2,7&lt;span style="font-size:12.0pt;font-family:&#xD;
Symbol;mso-ascii-font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" mso-hansi-font-family:"times="" roman";mso-bidi-font-family:"times="" mso-ansi-language:en-gb;mso-fareast-language:en-us;mso-bidi-language:ar-sa;="" mso-char-type:symbol;mso-symbol-font-family:symbol"="" lang="EN-GB"&gt;a&lt;span style="font-size:12.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:="" "times="" roman";mso-ansi-language:en-gb;mso-fareast-language:en-us;="" mso-bidi-language:ar-sa"="" lang="EN-GB"&gt;-tribromocholest-4-en-3,6-dione, &lt;b&gt;3&lt;/b&gt; and 2&lt;span style="font-size:12.0pt;font-family:Symbol;mso-ascii-font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-hansi-font-family:="" "times="" roman";mso-bidi-font-family:"times="" roman";mso-ansi-language:="" en-gb;mso-fareast-language:en-us;mso-bidi-language:ar-sa;mso-char-type:symbol;="" mso-symbol-font-family:symbol"="" lang="EN-GB"&gt;a&lt;span style="font-size:12.0pt;font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-ansi-language:="" en-gb;mso-fareast-language:en-us;mso-bidi-language:ar-sa"="" lang="EN-GB"&gt;,7&lt;span style="font-size:12.0pt;font-family:Symbol;mso-ascii-font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-hansi-font-family:="" "times="" roman";mso-bidi-font-family:"times="" roman";mso-ansi-language:="" en-gb;mso-fareast-language:en-us;mso-bidi-language:ar-sa;mso-char-type:symbol;="" mso-symbol-font-family:symbol"="" lang="EN-GB"&gt;a&lt;span style="font-size:12.0pt;font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-ansi-language:="" en-gb;mso-fareast-language:en-us;mso-bidi-language:ar-sa"="" lang="EN-GB"&gt;-dibromocholest-4-en-3,6-dione&#xD;
&lt;b&gt;4&lt;/b&gt; by various spectroscopic methods.&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;br/&gt;
&lt;br/&gt;Page(s): 1027-1031</description>
      <pubDate>Thu, 28 Jun 2012 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>&lt;span style="font-size:12.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-ansi-language: EN-GB;mso-fareast-language:EN-US;mso-bidi-language:AR-SA" lang="EN-GB"&gt;Synthesis, antimicrobial, insecticidal and anthelmintic activity studies of some new alkyl/aryl 6-(4-(4-(4-methyl-1&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;-1,2,3-triazol-1-yl)phenyl amino)phenyl)-N&lt;sup&gt;2&lt;/sup&gt;,N&lt;sup&gt;4&lt;/sup&gt;-bis(4-methoxyphenyl)-1,3,5-triazin-2,4-diamine carbamic acid ester derivatives&lt;/span&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/14359</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-GB;mso-fareast-language:EN-US;mso-bidi-language:AR-SA" lang="EN-GB"&gt;Synthesis, antimicrobial, insecticidal and anthelmintic activity studies of some new alkyl/aryl 6-(4-(4-(4-methyl-1&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;-1,2,3-triazol-1-yl)phenyl amino)phenyl)-N&lt;sup&gt;2&lt;/sup&gt;,N&lt;sup&gt;4&lt;/sup&gt;-bis(4-methoxyphenyl)-1,3,5-triazin-2,4-diamine carbamic acid ester derivatives&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Gautam, Nidhi; Chourasia, O P
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;span style="font-size:12.0pt;font-family:&#xD;
" times="" new="" roman";mso-fareast-font-family:"times="" roman";mso-ansi-language:="" en-gb;mso-fareast-language:en-us;mso-bidi-language:ar-sa"="" lang="EN-GB"&gt;New carbamic acid&#xD;
ester derivatives containing 1,2,3-triazole nucleus have been synthesized and&#xD;
their antimicrobial, insecticidal and anthelmintic activity investigated.&#xD;
6-(4-(4-Methyl-1&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;-5-carbonyl&#xD;
azide-1,2,3-triazol-1-yl)phenyl amino)phenyl-N&lt;sup&gt;2&lt;/sup&gt;-N&lt;sup&gt;4&lt;/sup&gt;-bis(-methoxy&#xD;
phenyl)-1,3,5-triazin-2, 4-diamine has been used as a precursor to synthesize&#xD;
some new alkyl/aryl 6-(4-(4-methyl-1&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;-1,2,3-triazol-1-yl)phenylamino)phenyl-N&lt;sup&gt;2&lt;/sup&gt;,N&lt;sup&gt;4&lt;/sup&gt;–bis(4-methoxyphenyl)-&#xD;
1,3,5-triazin-2,4-diamine carbamic acid ester derivatives. The compounds have&#xD;
been screened for their antibacterial efficacy against &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;B. subtilis, E. coli, K. pneumonie&lt;/i&gt; and &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;S. aureus&lt;/i&gt; and for their antifungal efficacy against &lt;i style="mso-bidi-font-style:normal"&gt;A. flavus, A. niger, F. oxysporum &lt;/i&gt;and &lt;i style="mso-bidi-font-style:normal"&gt;Trichoderma viridae&lt;/i&gt;. Insecticidal&#xD;
activity against &lt;i style="mso-bidi-font-style:normal"&gt;Periplaneta americana&lt;/i&gt; and&#xD;
anthelmintic activity against &lt;i style="mso-bidi-font-style:normal"&gt;Pheretima&#xD;
posthuma&lt;/i&gt; (Indian adult earthworm) have been studied.&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 1020-1026</description>
      <pubDate>Thu, 28 Jun 2012 22:58:59 GMT</pubDate>
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