Issue 9, 1998

Facial selectivity in the cycloaddition of heterodienes to carbohydrate cyclic ketene acetals. A novel synthesis of disaccharide derivatives

Abstract

Carbohydrate ketene acetals derived from mannopyranose and glucopyranose are shown to serve as electron-rich dienophiles in facially selective, Lewis acid-catalyzed inverse electron demand hetero-Diels–Alder reactions.

Article information

Article type
Paper

Chem. Commun., 1998, 1019-1020

Facial selectivity in the cycloaddition of heterodienes to carbohydrate cyclic ketene acetals. A novel synthesis of disaccharide derivatives

S. C. Johnson, Chem. Commun., 1998, 1019 DOI: 10.1039/A800103K

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