Issue 21, 1980
From the journal:

Journal of the Chemical Society, Chemical Communications

Asymmetric reduction of αβ-unsaturated ketones with lithium aluminium hydride partially decomposed by (–)-N-methylephedrine and N-ethylaniline

Shiro Terashima,   Norihiko Tanno  and  Kenji Koga  

Abstract

The title asymmetric reaction is found to convert open chain enones into the corresponding optically active allylic alcohols in high optical (78–98% enantiomeric excess) and chemical (92–100%) yields.

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Article information

DOI
https://doi.org/10.1039/C39800001026
Article type
Paper

J. Chem. Soc., Chem. Commun., 1980, 1026-1027

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Asymmetric reduction of αβ-unsaturated ketones with lithium aluminium hydride partially decomposed by (–)-N-methylephedrine and N-ethylaniline

S. Terashima, N. Tanno and K. Koga, J. Chem. Soc., Chem. Commun., 1980, 1026 DOI: 10.1039/C39800001026

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