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

DOI: 10.1016/S0040-4039(96)02308-8

Source and publish data:

Tetrahedron Letters p. 241 - 244 (1997)

Update date:2022-08-04

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Authors:

Magaud, Didier

Grandjean, Cyrille

Doutheau, Alain

Anker, Daniel

Shevchik, Vladimir

Cotte-Pattat, Nicole

Robert-Baudouy, Janine

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Article abstract of DOI:10.1016/S0040-4039(96)02308-8

The highly stereoselective α(1 → 4) coupling between two D-galacturonic acid ester derivatives was accomplished in good yields, for the first time, using a phenylthioglycoside as donor. The method was designed to prepare D-galacturonic acid oligomers with methyl ester groups in definite positions.

Full text of DOI:10.1016/S0040-4039(96)02308-8

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