Issue 17, 1987

Cycloaddition reactions of oximes; powerful new carbon–carbon bond forming methodology

Abstract

Oximes react with Michael acceptors and dipolarophiles, usually regio- and stereo-specifically, via a tandem Michael addition–1,3-dipolar cycloaddition process, to give isoxazolidines in good yield; analysis of the tandem process identifies four broad synthetic variants, and examples of those involving initial intermolecular Michael addition are given.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 1325-1327

Cycloaddition reactions of oximes; powerful new carbon–carbon bond forming methodology

P. Armstrong, R. Grigg and W. J. Warnock, J. Chem. Soc., Chem. Commun., 1987, 1325 DOI: 10.1039/C39870001325

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