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.

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