Issue 10, 1983

Enantiospecific syntheses of trifunctional (R)-3-hydroxy esters by baker's yeast reduction

Abstract

Asymmetric syntheses of the enantiomerically pure trifunctional (R)-3-hydroxy esters (7)–(10) can be achieved by baker's yeast reduction of the hydrolysed β-keto carboxylates (2)–(5) instead of by reduction of the corresponding ester.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 599-600

Enantiospecific syntheses of trifunctional (R)-3-hydroxy esters by baker's yeast reduction

M. Hirama, M. Shimizu and M. Iwashita, J. Chem. Soc., Chem. Commun., 1983, 599 DOI: 10.1039/C39830000599

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