http://192.168.1.40:8080/xmlui/handle/123456789/1433 Fri, 04 Sep 2026 07:07:20 GMT 2026-09-04T07:07:20Z http://192.168.1.40:8080/xmlui/handle/123456789/1932 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. Thu, 01 Jan 2009 00:00:00 GMT http://192.168.1.40:8080/xmlui/handle/123456789/1932 2009-01-01T00:00:00Z http://192.168.1.40:8080/xmlui/handle/123456789/1924 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. Thu, 01 Jan 2009 00:00:00 GMT http://192.168.1.40:8080/xmlui/handle/123456789/1924 2009-01-01T00:00:00Z http://192.168.1.40:8080/xmlui/handle/123456789/1922 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 Wed, 11 Mar 2009 00:00:00 GMT http://192.168.1.40:8080/xmlui/handle/123456789/1922 2009-03-11T00:00:00Z http://192.168.1.40:8080/xmlui/handle/123456789/1919 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 Thu, 15 Jan 2009 00:00:00 GMT http://192.168.1.40:8080/xmlui/handle/123456789/1919 2009-01-15T00:00:00Z