Issue 15, 1978

Microbial stereo-differentiating reduction of the carbonyl groups located on the C2 axes of gyrochiral molecules

Abstract

Stereochemistry of microbial reduction (Curvularia lunata and Rhodotorula rubra) of the gyrochiral ketones whose C2 axes coincide with the carbonyl axes was examined to reveal a remarkable enantiomer selectivity.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 667-668

Microbial stereo-differentiating reduction of the carbonyl groups located on the C2 axes of gyrochiral molecules

M. Nakazaki, H. Chikamatsu, K. Naemura, M. Nishino, H. Murakami and M. Asao, J. Chem. Soc., Chem. Commun., 1978, 667 DOI: 10.1039/C39780000667

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