Issue 8, 1988

Straightforward route to 2- and 3-formyl hex-1- and -2-enopyranosides and their highly stereoselective hetero Diels–Alder reaction with ethyl vinyl ether

Abstract

A straightforward route from D-glucose to conjugated enal and diene pyranoses through a dithiane-based methodology is disclosed; hetero Diels–Alder reaction of the enals with ethyl vinyl ether occurs with high stereoselectivity.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 514-515

Straightforward route to 2- and 3-formyl hex-1- and -2-enopyranosides and their highly stereoselective hetero Diels–Alder reaction with ethyl vinyl ether

J. C. Lopez, E. Lameignere and G. Lukacs, J. Chem. Soc., Chem. Commun., 1988, 514 DOI: 10.1039/C39880000514

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