<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns="http://purl.org/rss/1.0/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#">
<channel rdf:about="http://192.168.1.40:8080/xmlui/handle/123456789/1433">
<title>Anup Kumar Misra</title>
<link>http://192.168.1.40:8080/xmlui/handle/123456789/1433</link>
<description/>
<items>
<rdf:Seq>
<rdf:li rdf:resource="http://192.168.1.40:8080/xmlui/handle/123456789/1932"/>
<rdf:li rdf:resource="http://192.168.1.40:8080/xmlui/handle/123456789/1924"/>
<rdf:li rdf:resource="http://192.168.1.40:8080/xmlui/handle/123456789/1922"/>
<rdf:li rdf:resource="http://192.168.1.40:8080/xmlui/handle/123456789/1919"/>
</rdf:Seq>
</items>
<dc:date>2026-05-31T12:08:13Z</dc:date>
</channel>
<item rdf:about="http://192.168.1.40:8080/xmlui/handle/123456789/1932">
<title>Odorless regioselctive ring opening of epoxides with S-alkylisothiouronium salts as masked thiols in water</title>
<link>http://192.168.1.40:8080/xmlui/handle/123456789/1932</link>
<description>Odorless regioselctive ring opening of epoxides with S-alkylisothiouronium salts as masked thiols in water
Panchadhayee, Rajib; Misra, Anup Kumar
Opening of epoxides with various S-alkylisothiouronium salts as thiol equivalent in water has been carried out in excellent yield following an environmentally benign odorless reaction condition. Yields were excellent in every case.
</description>
<dc:date>2009-01-01T00:00:00Z</dc:date>
</item>
<item rdf:about="http://192.168.1.40:8080/xmlui/handle/123456789/1924">
<title>Facile synthesis of a tetrasaccharide corresponding to the capsular polysaccharide of Streptococcus pneumoniae type 15B</title>
<link>http://192.168.1.40:8080/xmlui/handle/123456789/1924</link>
<description>Facile synthesis of a tetrasaccharide corresponding to the capsular polysaccharide of Streptococcus pneumoniae type 15B
Mandal, Pintu Kumar; Maiti, Gour Hari; Misra, Anup Kumar
A convergent synthetic approach is presented for the straightforward synthesis of the tetrasaccharide fragment of the capsular polysaccharide of Streptococcus pneumoniae type 15B. Coupling of a disaccharide thioglycoside donor with a disaccharide acceptor furnished the required tetrasaccharide in excellent yield.
</description>
<dc:date>2009-01-01T00:00:00Z</dc:date>
</item>
<item rdf:about="http://192.168.1.40:8080/xmlui/handle/123456789/1922">
<title>Total synthesis of a unique tetrasaccharide present in the human clotting factor IX and mammalian Notch 1 receptor</title>
<link>http://192.168.1.40:8080/xmlui/handle/123456789/1922</link>
<description>Total synthesis of a unique tetrasaccharide present in the human clotting factor IX and mammalian Notch 1 receptor
Mukherjee, Chinmoy; Misra, Anup Kumar
The Synthesis Of a unique tetrasaccharide linked to the serine 61 of human clotting factor IX through an alpha-L-fucose residue has been achieved for the first time in excellent yield. All glycosylation and protecting group manipulation steps are high yielding and reproducible for a scale-Lip preparation. A sequential glycosylation strategy has been used to assemble suitably protected monosaccharide synthons for the preparation of the target tetrasaccharide.
DOI: 10.1016/j.tetasy.2009.02.003
</description>
<dc:date>2009-03-11T00:00:00Z</dc:date>
</item>
<item rdf:about="http://192.168.1.40:8080/xmlui/handle/123456789/1919">
<title>Syntheses and evaluation of glucosyl aryl thiosemicarbazide and glucosyl thiosemicarbazone derivatives as antioxidant and anti-dyslipidemic agents</title>
<link>http://192.168.1.40:8080/xmlui/handle/123456789/1919</link>
<description>Syntheses and evaluation of glucosyl aryl thiosemicarbazide and glucosyl thiosemicarbazone derivatives as antioxidant and anti-dyslipidemic agents
Ghosh, Samir; Misra, Anup Kumar; Bhatia, Gitika; Khan, M. M; Khanna, A. K
A series of N-per-O-acetyl-glucosyl arylthiosemicarbazide and thiosemicarbazone derivatives have been synthesized and evaluated for their in vivo anti-dyslipidemic and in vitro antioxidant activities. Among 16 compounds tested, 3 compounds showed potent anti-dyslipidemic activity and 6 compounds showed potent antioxidant and scavenger of oxygen free radicals activity.
DOI: 10.1016/j.bmcl.2008.11.070
</description>
<dc:date>2009-01-15T00:00:00Z</dc:date>
</item>
</rdf:RDF>
