Asymmetric reduction of alkyl phenyl ketones with a chiral hydride reagent prepared from lithium aluminum hydride and (S)-4-anilino-3-methylamino-1-butanol-Reference-Cited by-同舟云学术

Asymmetric reduction of alkyl phenyl ketones with a chiral hydride reagent prepared from lithium aluminum hydride and (S)-4-anilino-3-methylamino-1-butanol

Published:1982-01 Issue:40 Volume:23 Page:4111-4112
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Sato Toshio,Goto Yoshihiko,Fujisawa Tamotsu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference8 articles.

1. Asymmetric Synthesis

2. Recent advances in asymmetric synthesis

3. Asymmetric synthesis. Part III. The reduction of ketones with the ethanol modified lithium aluminium hydride-3-O-benzyl-1,2-O-cyclohexylidene-α-D-glucofuranose complex

4. Virtually complete enantioface differentiation in carbonyl group reduction by a complex aluminum hydride reagent

5. ASYMMETRIC REDUCTION OF SIMPLE ACHIRAL KETONES WITH LITHIUM ALUMINUM HYDRIDE PARTIALLY DECOMPOSED BY (−)-N-METHYLEPHEDRINE ANDN-ETHYLANILINE

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