Efficient synthesis of the deoxysugar part of versipelostatin by direct and stereoselective glycosylation and revision of the structure of the trisaccharide unit

Chemistry - An Asian Journal

Volumn 4, Issue 7, 2009, Pages 1114-1125

  Tanaka, Hiroshi ^a   Yoshizawa, Atsushi ^a   Chijiwa, Shuhei ^b   Ueda, Jun Ya ^b   Takagi, Motoki ^b   Shin ya, Kazuo ^c   Takahashi, Takashi ^a  

^a TOKYO INSTITUTE OF TECHNOLOGY   (Japan)

^b Koto ku   (Japan)

^c NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY AIST   (Japan)

Author keywords

Glycosides; Glycosylation; Iodine; Oxidative activation; Synthetic methods

Indexed keywords

ANOMERIZATION; BASIC CONDITIONS; BIOLOGICAL ACTIVITIES; BIOLOGICAL ASSAYS; DEOXYSUGAR; EFFICIENT SYNTHESIS; GLYCOSIDES; OXIDATIVE ACTIVATION; STEREO-SELECTIVE; SYNTHETIC METHODS; VERSIPELOSTATIN;

ESTERIFICATION; INDUSTRIAL CHEMICALS; IODINE; STEREOSELECTIVITY; SUGARS;

GLYCOSYLATION;

DEOXYSUGAR; MACROLIDE; OLIGOSACCHARIDE; TRISACCHARIDE; VERSIPELOSTATIN;

ARTICLE; CHEMISTRY; CONFORMATION; GLYCOSYLATION; HELA CELL; HUMAN; STEREOISOMERISM; SYNTHESIS; TUMOR CELL LINE;

CELL LINE, TUMOR; DEOXY SUGARS; GLYCOSYLATION; HELA CELLS; HUMANS; MACROLIDES; MOLECULAR CONFORMATION; OLIGOSACCHARIDES; STEREOISOMERISM; TRISACCHARIDES;

EID: 68349104975     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.200800448     Document Type: Article

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