A chiral oxazaborolidinone-promoted aldol reaction with a silyl ketene acetal from ethyl 1,3-dithiolane-2-carboxylate. Synthesis of acetate aldols in high enantiomeric purity-Reference-Cited by-同舟云学术

A chiral oxazaborolidinone-promoted aldol reaction with a silyl ketene acetal from ethyl 1,3-dithiolane-2-carboxylate. Synthesis of acetate aldols in high enantiomeric purity

Published:1996-08 Issue:8 Volume:7 Page:2181-2184
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Kiyooka Syun-ichi,Hena Mostofa Abu

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference19 articles.

1. Catalytic, Enantioselective Aldol Additions with Methyl and Ethyl Acetate O-Silyl Enolates: A Chiral Tridentate Chelate as a Ligand for Titanium(IV)

2. Asymmetric Catalytic Aldol-type Reaction with Ketene Silyl Acetals: Possible Intervention of the Silatropic Ene Pathway

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

4. Chiral Lewis Acid-Controlled Synthesis of Both Diastereomers. Enantioselective Synthesis of Both syn- and anti-2,3-Dihydroxy Ester Derivatives from the Same Starting Materials via Asymmetric Aldol Reactions by Choice of Chiral Ligands

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

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