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An efficient and highly stereoselective α(1→4) glycosylation between two d-galacturonic acid ester derivatives

✍ Scribed by Didier Magaud; Cyrille Grandjean; Alain Doutheau; Daniel Anker; Vladimir Shevchik; Nicole Cotte-Pattat; Janine Robert-Baudouy

Book ID: 104256056
Publisher: Elsevier Science
Year: 1997
Tongue: French
Weight: 267 KB
Volume: 38
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(96)02308-8

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✦ Synopsis

The highly stercoselective a(1-->4) coupling between two D-galacturonic acid ester derivetives was accomplished in good yields, for the first time. using a phenylthioglycoside as donor. The method was designed to prepsre D-galacturonic acid oHgomers with methyl ester groups in definite positions.

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