Abstract
Some O- D-glucopyranosyl-, O- D-galactopyranosyl-, and O- D-galactofuranosyl- L-serine derivatives have been synthesised by the Königs-Knorr and orthoester methods of glycosylation. The stability of the glycosidic bond in acid and alkali has been determined in order to demonstrate the influence of substituents on the amino and carboxyl groups of the serine moiety.
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