Issue 13, 1985

Asymmetric Diels–Alder reactions of sulphinyl-activated dienophiles obtained via a self-induced chiral oxidation

Abstract

The Diels–Alder cycloaddition of activated vinyl sulphoxides (1), that are readily obtained by a self-induced chiral oxidation, proceeds highly diastereoselectively to form the corresponding cycloadducts (4) that can be converted into 2-substituted norbornadienes(5) of high enantiomeric purity.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 878-880

Asymmetric Diels–Alder reactions of sulphinyl-activated dienophiles obtained via a self-induced chiral oxidation

O. De Lucchi, C. Marchioro, G. Valle and G. Modena, J. Chem. Soc., Chem. Commun., 1985, 878 DOI: 10.1039/C39850000878

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