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Studies on the alkylation of enolates derived from a range of W-acyl-5,5-dimethyloxazolidin-2-ones and N-acyl-5,5diphenyloxazolidin-2-ones reveal that high yields and high diastereoselectivities are best obtained when homochiral 4-isopropyl-5,5-dimethyIoxazolidin-2-one is employed as a chiral auxiliary.

Original publication

DOI

10.1039/a809715a

Type

Journal article

Journal

Journal of the Chemical Society - Perkin Transactions 1

Publication Date

01/01/1999

Pages

387 - 398