Tetrahedron Letters p. 1241 - 1244 (1984)
Update date:2022-08-04
Topics: Regioselectivity Chiral Stereochemistry Reduction Enantioselectivity Enantiomeric excess (ee) Ketone Biocatalysis Substrate Chiral Auxiliary Fermentation Prochiral Diol Racemic mixture Optical activity Cyclohexanediones
Brooks, Dee W.
Mazdiyasni, Hormoz
Chakrabarti, Sharmistha
Microbial reduction of various 2,2-disubstituted-1,3-cyclohexanediones with bakers' yeast provides efficient access to chiral cyclohexanoid synthetic precursors.
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