Issue 23, 1983

An examination of the extent of diasterofacial selection in the reactions of a chiral nitrile oxide with achiral alkenes: a route to β-hydroxy carboxylic acids

Abstract

A new synthesis of optically active β-hydroxy carboxylic acids has been developed which is based on the (modest) diastereoselective addition of the chiral nitrile oxide (4) to 1,2-disubstituted alkenes.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 1460-1462

An examination of the extent of diasterofacial selection in the reactions of a chiral nitrile oxide with achiral alkenes: a route to β-hydroxy carboxylic acids

A. P. Kozikowski, Y. Kitagawa and J. P. Springer, J. Chem. Soc., Chem. Commun., 1983, 1460 DOI: 10.1039/C39830001460

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