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    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.51B(08) [August 2012]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/14492</link>
    <description />
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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;Green synthesis of novel isoxazoline derivatives using &lt;i style="mso-bidi-font-style:normal"&gt;N&lt;/i&gt;-methyl-α-chloro nitrone and their antibacterial activities &lt;/span&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/14517</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;Green synthesis of novel isoxazoline derivatives using &lt;i style="mso-bidi-font-style:normal"&gt;N&lt;/i&gt;-methyl-α-chloro nitrone and their antibacterial activities &lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Chakraborty, Bhaskar; Sharma, Prawin Kumar; Samanta, Amalesh
&lt;br/&gt;
&lt;br/&gt;Abstract: Microwave assisted 1,3-dipolar&#xD;
cycloaddition reaction of &lt;i style="mso-bidi-font-style:normal"&gt;N&lt;/i&gt;-methyl-α-chloro&#xD;
nitrone with various alkynes as dipolarophile have been studied and found to&#xD;
afford diastereomeric novel isoxazoline derivatives with high selectivity.&lt;i style="mso-bidi-font-style:normal"&gt; &lt;/i&gt;All the synthesized compounds have been&#xD;
screened for their antibacterial activity and are found to exihibit significant&#xD;
activity.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1180-1185</description>
      <pubDate>Sun, 29 Jul 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;Ultrasound and microwave assisted rapid and sustainable route to synthesis of benzothiazine derivatives&lt;/span&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/14516</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;Ultrasound and microwave assisted rapid and sustainable route to synthesis of benzothiazine derivatives&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Dabholkar, Vijay V; avande, Rahul P G
&lt;br/&gt;
&lt;br/&gt;Abstract: Ultrasound and microwave assisted synthesis&#xD;
of 2-Meldrum-2&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;,4&lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;H&lt;/i&gt;-2-carbonyl methyl-3-oxo-1,4-benzothiazine 10, 2-dimi-done-2&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;,4&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;-2-carbonyl&#xD;
methyl-3-oxo-1,4-benzothiazine 11, 2&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;,4&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;-2-amino-[3-methyl&#xD;
pyrazol-5-one-1-yl]-carbonyl methyl-3-oxo-1,4-benzothiazine 12,2&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;,4&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;-2-amino-[3,5-dmethyl&#xD;
pyra­zol-1-yl]-carbonyl methyl-3-oxo-1,4-benzothiazine 13 and 2&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;, 4&lt;i style="mso-bidi-font-style:normal"&gt;H&lt;/i&gt;-2-amino-[3-phenyl,&#xD;
5-methyl pyrazol-1-yl]-carbonyl methyl-3-oxo-1,4-benzothiazine 14 from 2-amino­benzene­thiol&#xD;
and 1,3 diketo compounds containing active methylene group have been carried&#xD;
out. All the synthesized compounds have been investigated for their&#xD;
antibacterial activities. The result indicate that the compounds show convincing&#xD;
activities against Gram-positive bacteria (&lt;i style="mso-bidi-font-style:normal"&gt;Bacillus&#xD;
subtilis &lt;/i&gt;and&lt;i style="mso-bidi-font-style:normal"&gt; Streptococcus lactis&lt;/i&gt;)&#xD;
when compared with standard drug (ampicillin trihydrate). These compounds have&#xD;
been also synthesized by conventional method and their structures have been&#xD;
elucidated on the basis of spectral analyses and chemical reactions.
&lt;br/&gt;
&lt;br/&gt;Page(s): 1173-1179</description>
      <pubDate>Sun, 29 Jul 2012 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Zinc chloride promoted efficient and facile BOC protection of amines</title>
      <link>http://nopr.niscair.res.in/handle/123456789/14515</link>
      <description>Title: Zinc chloride promoted efficient and facile BOC protection of amines
&lt;br/&gt;
&lt;br/&gt;Authors: Arifuddin, M; Lakshmikant, N; Rajasekar, N; Shinde, D B
&lt;br/&gt;
&lt;br/&gt;Abstract: Amines are efficiently protected as their BOC&#xD;
derivatives under mild reaction conditions when reacted with BOC anhydride in&#xD;
presence of ZnCl&lt;sub&gt;2&lt;/sub&gt;. The present method is applicable to a variety of&#xD;
amines including aliphatic, aromatic as well as heteroaromatic amines. T&lt;span style="mso-ansi-language:EN-US" lang="EN-US"&gt;his protocol appears to be&#xD;
competitive and in some cases superior to previously reported procedures that&#xD;
work under basic conditions.&#xD;
&#xD;
&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 1168-1172</description>
      <pubDate>Sun, 29 Jul 2012 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Iodine catalysed aza-Michael addition of carbamates to chalcones</title>
      <link>http://nopr.niscair.res.in/handle/123456789/14514</link>
      <description>Title: Iodine catalysed aza-Michael addition of carbamates to chalcones
&lt;br/&gt;
&lt;br/&gt;Authors: Deuri, Sanjib; Kataki, Dolly; Phukan, Prodeep
&lt;br/&gt;
&lt;br/&gt;Abstract: Iodine has been found to&#xD;
catalyze the aza-Michael reaction of chalcones with weaker nucleophile&#xD;
carbamates. Although iodine alone can promote the reaction, addition of TMSCl&#xD;
enhances the yield of the product. A variety of chalcones have been reacted with&#xD;
benzyl carbamate to produce &lt;span style="font-family:Symbol;&#xD;
mso-ascii-font-family:" times="" new="" roman";mso-hansi-font-family:"times="" roman";="" mso-char-type:symbol;mso-symbol-font-family:symbol"="" lang="EN-GB"&gt;b-amino-carbonyl&#xD;
compounds in high yield.&#xD;
&#xD;
&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 1163-1167</description>
      <pubDate>Sun, 29 Jul 2012 22:58:59 GMT</pubDate>
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