Synthesis of specifically deoxygenated analogues of the methyl α-glycoside of the intracatenary monosaccharide repeating unit of the O-polysaccharide of Vibrio cholerae O:1

Article abstract of DOI:10.1016/0008-6215(94)00319-B

Treatment of methyl α-D-perosaminide (1) with γ-butyrolactone gave the 2'-deoxy analogue of methyl 4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-mannopyranoside (13), the methyl α-glycoside of the intracatenary monosaccharide repeating unit of the O-p