Issue 17, 1990

Asymmetric reduction of prochiral aromatic ketones by Borane–Amine complexes in the presence of a chiral amine–BF3 catalyst

Abstract

The (–)-N-α-Methylbenzyl-3,5-dihydrodinaphthazepine–BH3 complex reduces aromatic ketones to alcohols with 11–57% enantiomeric excess (e.e.) in the presence of BF3·OEt2, the (–)-N-α-methylbenzyl-3,5 dihydrodinaphthazepine–BF3 complex catalyses asymmetric reduction of acetophenone by N,N′-diethylaniline–BH3 to give α-phenylethyl alcohol in 51% e.e.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 1145-1147

Asymmetric reduction of prochiral aromatic ketones by Borane–Amine complexes in the presence of a chiral amine–BF3 catalyst

J. V. B. Kanth and M. Periasamy, J. Chem. Soc., Chem. Commun., 1990, 1145 DOI: 10.1039/C39900001145

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements