The catalytic asymmetric aldol reaction of silyl ketene acetals with aldehydes in the presence of a chiral borane complex. Nitroethane as a highly effective solvent for catalytic conditions-Reference-Cited by-同舟云学术

The catalytic asymmetric aldol reaction of silyl ketene acetals with aldehydes in the presence of a chiral borane complex. Nitroethane as a highly effective solvent for catalytic conditions

Published:1992-08 Issue:34 Volume:33 Page:4927-4930
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kiyooka Syun-ichi,Kaneko Yuichi,Kume Ken-ichi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference14 articles.

1. Chiral Lewis Acids in Catalytic Asymmetric Reactions

2. Catalytic asymmetric aldol reactions. Use of a chiral (acyloxy)borane complex as a versatile Lewis-acid catalyst

3. Chiral (Acyloxy)borane Catalyzed Asymmetric Aldol Type Reaction of Ketene Silyl Acetals with Aldehydes

4. Asymmetric aldol reaction between achiral silyl enol ethers and achiral aldehydes by use of a chiral promoter system

5. Enantioselective chiral borane-mediated aldol reactions of silyl ketene acetals with aldehydes. The novel effect of the trialkysilyl group of the silyl ketene acetal on the reaction course

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