Syntheses of linear tetra-, hexa-, and octa-saccharide fragments of the i-blood group active poly-(N-acetyl-lactosamine) series. Blockwise methods for the synthesis of repetitive oligosaccharide sequences.

DOI: 10.1016/0008-6215(90)80002-K

Source and publish data:

Carbohydrate research p. 11 - 31 (1990)

Update date:2022-07-29

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Authors:

Alais Alais

Veyrieres

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Article abstract of DOI:10.1016/0008-6215(90)80002-K

N-Phthaloylation of lactosamine gave various glycosyl donors (beta-chloride, beta-trichloroacetimidate) and glycosyl acceptors (3',4'-diol). Coupling of the chloride with a methyl beta-D-glycoside led to the tetrasaccharide fragment, beta-D-Galp-(1----4)-

Full text of DOI:10.1016/0008-6215(90)80002-K

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