Issue 18, 1991

Enantiocontrolled reduction of prochiral aromatic ketones with borane using diastereoisomeric secondary aminoalcohols as chiral catalysts

Abstract

Exo- and endo-2-hydroxy-3-(1-methyl-2-pyrrolyl)methylaminobornanes were found to be efficient catalysts for enantioselective borane reduction of prochiral aromatic ketones with predictable absolute stereochemistry.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 1311-1312

Enantiocontrolled reduction of prochiral aromatic ketones with borane using diastereoisomeric secondary aminoalcohols as chiral catalysts

K. Tanaka, J. Matsui and H. Suzuki, J. Chem. Soc., Chem. Commun., 1991, 1311 DOI: 10.1039/C39910001311

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