Issue 2, 1996

Nucleophilic displacements on a cyclic sulfamidate derived from allosamine: application to the synthesis of thiooligosaccharides

Abstract

The cyclic sulfamidate of the allosamine derivative 11 is efficiently prepared by reaction with 1,1′-sulfuryl diimidazole; the regioselective opening of this compound by sulfur nucleophiles furnishes 3-thioglucosamine derivatives, useful intermediates in synthesis of thiooligosaccharides.

Article information

Article type
Paper

Chem. Commun., 1996, 127-128

Nucleophilic displacements on a cyclic sulfamidate derived from allosamine: application to the synthesis of thiooligosaccharides

B. Aguilera and A. Fernández-Mayoralas, Chem. Commun., 1996, 127 DOI: 10.1039/CC9960000127

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