Issue 19, 1987

Asymmetric oxidation by new cyclic flavins with planar chirality (chiral flavinophanes)

Abstract

Cyclic flavins with planar chirality (chiral flavinophanes) can oxidise thiols (ca. 43% enantiomeric excess) and NADH model compounds (ca. 60% enantiomeric excess) in an asymmetric manner.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 1506-1508

Asymmetric oxidation by new cyclic flavins with planar chirality (chiral flavinophanes)

S. Shinkai, T. Yamaguchi, A. Kawase, A. Kitamura and O. Manabe, J. Chem. Soc., Chem. Commun., 1987, 1506 DOI: 10.1039/C39870001506

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