The Michael Reaction of O-Silylated Ketene Acetals with α,β-Unsaturated Esters Promoted by a Catalytic Amount of Aluminum Triflate
Authors:
- 5 September 1987
- journal article
- research article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 16 (9) , 1719-1722
Abstract
The Michael reaction of O-silylated ketene acetals with α,β-unsaturated ester in the presence of a catalytic amount of aluminum triflate proceeds smoothly under mild conditions to afford the corresponding glutarates in good yields.Keywords
This publication has 2 references indexed in Scilit:
- A highly stereoselective Michael reaction of simple ester enolates to α,β-unsaturated estersTetrahedron Letters, 1984
- The Michael Reaction of Silyl Enol Ethers with α,β-Unsaturated Eetones and Acetals in the Presence of Titanium Tetraalkoxide and Titanium TetrachlorideBulletin of the Chemical Society of Japan, 1976