Tetrahedron Letters p. 241 - 244 (1997)
Update date:2022-08-04
Topics:
Magaud, Didier
Grandjean, Cyrille
Doutheau, Alain
Anker, Daniel
Shevchik, Vladimir
Cotte-Pattat, Nicole
Robert-Baudouy, Janine
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.
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Doi:10.1016/0277-5387(96)00277-X
(1997)Doi:10.1016/S0020-1693(96)05339-X
(1997)Doi:10.1007/BF00568526
()Doi:10.1007/BF00910810
()Doi:10.1021/ja963114c
(1997)Doi:10.1021/jo01264a014
(1969)
