ChemInform Abstract: An Efficient and Highly Stereoselective α(1 → 4) Glycosylation Between Two D-Galacturonic Acid Ester Derivatives.
✍ Scribed by D. MAGAUD; C. GRANDJEAN; A. DOUTHEAU; D. ANKER; V. SHEVCHIK; N. COTTE-PATTAT; J. ROBERT-BAUDOUY
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 34 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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Synthesis of the Two Monomethyl Esters of the Disaccharide 4-O-α-D-Galacturonosyl-D-galacturonic Acid and of Precursors for the Preparation of Higher Oligomers Methyl Uronated in Definite Sequences. -Direct coupling of two D-galacturonic acid esters is achieved using thioglycosides such as (VII) and