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Highly Enantioselective Intermolecular Stetter Reactions of β-Aryl Acceptors: α-Ketoester Moiety as Handle for Activation and Synthetic Manipulations

Authors :
Karen Thai
Michel Gravel
François Bilodeau
Eduardo Sánchez-Larios
Source :
Organic Letters. 13:4942-4945
Publication Year :
2011
Publisher :
American Chemical Society (ACS), 2011.

Abstract

The use of β,γ-unsaturated-α-ketoesters in the intermolecular Stetter reaction furnishes 1,2,5-tricarbonyl compounds in high yield and excellent enantioselectivity. The α,δ-diketoesters generated using this methodology serve as useful synthetic building blocks via chemo- and diastereoselective transformations.

Details

ISSN :
15237052 and 15237060
Volume :
13
Database :
OpenAIRE
Journal :
Organic Letters
Accession number :
edsair.doi.dedup.....fe246144924b5e6ed4c10ed80f8a032b