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Chromatographic separation of Lewis a and Lewis x oligosaccharides as glycosynthons

✍ Scribed by Natacha Frison; Laurent Meunier; Philippe Marceau; Christophe Quétard; Gérard Strecker; Annie-Claude Roche; Roger Mayer; Michel Monsigny

Book ID: 117456881
Publisher: Elsevier Science
Year: 2003
Tongue: English
Weight: 195 KB
Volume: 85
Category: Article
ISSN: 0300-9084
DOI: 10.1016/s0300-9084(03)00073-7

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Chemoenzymatic synthesis of GM3, Lewis x

Chemoenzymatic synthesis of GM3, Lewis x and sialyl Lewis x oligosaccharides in 13C-enriched form

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In connection with studies on the solution and protein-bound conformation of oligosaecharides, we had reason to consider the application of 13C-enriched sugars. Herein we describe the synthesis of ganglioside GM3 trisaccharide (1), Lewis x trisaccharide (2) and the sialyl Lewis x tetrasaccharide (3)

Syntheses of Lewis X and Dimeric Lewis X

Syntheses of Lewis X and Dimeric Lewis X : Construction of Branched Oligosaccharides by a Combination of Preactivation and Reactivity Based Chemoselective One-Pot Glycosylations

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Conformational studies of Lewis X and Le

Conformational studies of Lewis X and Lewis A trisaccharides using NMR residual dipolar couplings

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ChemInform Abstract: Synthesis of N-Acet

ChemInform Abstract: Synthesis of N-Acetylglucosamine Containing Lewis A and Lewis X Building Blocks Based on N-Tetrachlorophthaloyl Protection — Synthesis of Lewis X Pentasaccharide.

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