ASYMMETRIC REDUCTION OF PROCHIRAL CYCLIC KETONES WITH LITHIUM ALUMINUM HYDRIDE PARTIALLY DECOMPOSED BY (1R,2S)-(−)-N-METHYLEPHEDRINE AND 2-ALKYLAMINOPYRIDINE-Reference-Cited by-同舟云学术

ASYMMETRIC REDUCTION OF PROCHIRAL CYCLIC KETONES WITH LITHIUM ALUMINUM HYDRIDE PARTIALLY DECOMPOSED BY (1R,2S)-(−)-N-METHYLEPHEDRINE AND 2-ALKYLAMINOPYRIDINE

Published:1984-02-05 Issue:2 Volume:13 Page:239-242
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Kawasaki Motoji,Suzuki Yasutaka,Terashima Shiro

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference12 articles.

1. Recent advances in asymmetric synthesis

2. Asymmetric reduction of various types of ketones with lithium aluminum hydride partially decomposed with (-)-N-methylephedrine and N-ethylaniline.

3. Asymmetric reductions with chiral reagents from lithium aluminum hydride and (+)-(2S,3R)-4-dimethylamino-3-methyl-1,2-diphenyl-2-butanol

4. Reduction asymetrique de cetones par des alcoxyaluminohydrures chiraux prepares a partir de l'ephedrine et divers alcools ou phenols achiraux

5. An Asymmetric Reduction of Prochiral Ketones with a Chiral Hydride Reagent Prepared from Lithium Aluminium Hydride and (S)-2-(2,6-Xylidinomethyl)pyrrolidine

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