ASYMMETRIC REDUCTION OF PROCHIRAL KETO ESTERS WITH A CHIRAL REDUCING AGENT PREPARED FROM TIN(II) CHLORIDE, CHIRAL DIAMINE, AND DIISOBUTYLALUMINUM HYDRIDE-Reference-Cited by-同舟云学术

ASYMMETRIC REDUCTION OF PROCHIRAL KETO ESTERS WITH A CHIRAL REDUCING AGENT PREPARED FROM TIN(II) CHLORIDE, CHIRAL DIAMINE, AND DIISOBUTYLALUMINUM HYDRIDE

Published:1985-06-05 Issue:6 Volume:14 Page:813-816
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Mukaiyama Teruaki,Tomimori Koji,Oriyama Takeshi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference19 articles.

1. Synthese von vier chiralen, elektrophilen C3- und C4-Synthesebausteinen aus Hydroxycarbonsäuren

2. Studies directed toward the total synthesis of streptogramin antibiotics. Enantiospecific approach to the nine-membered macrocycle of griseoviridin

3. Synthesis of optically active forms of ipsdienol and ipsenol

4. Synthesis of 6S, 7S-anhydro-serricornine.

5. Asymmetric reductinon of carbonyl compounds by yeast. II. Preparation of optically active α- and β-hydroxy carboxylic acid derivatives

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