Synthesis of methyl α-glycosides of some higher oligosaccharide fragments of the O-antigen of Vibrio cholerae O1, serotype Inaba and Ogawa

DOI: 10.1016/S0008-6215(97)00070-0

Source and publish data:

Carbohydrate Research p. 329 - 339 (1997)

Update date:2022-07-31

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Authors:

Zhang, Jian

Kovac, Pavol

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Article abstract of DOI:10.1016/S0008-6215(97)00070-0

The title oligosaccharides, the tri- through the hexasaccharide in the Inaba series and the penta- and the hexasaccharide in the Ogawa series, have been synthesized using 1-thioglycosides of precursors to 3-O-benzyl-perosamine (4-amino-4,6-dideoxy-D-manno

Full text of DOI:10.1016/S0008-6215(97)00070-0

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Product name:methyl 3-O-benzyl-4-(2,4-O-benzylidene-3-deoxy-L-glycero-tetronamido)-4,6-dideoxy-α-D-mannopyranosyl)-(1->2)-3-O-benzyl-4-(2,4-O-benzylidene-3-deoxy-L-glycero-tetronamido)-4,6-dideoxy-α-D-mannopyranosyl-(1->2)-3-O-benzyl-...

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