The Stereoselective Michael Reaction of α,β-Unsaturated Thioesters with Silyl Enol Ethers Promoted by Combined Use of Antimony(V) Chloride and Tin(II) Triflate
- 5 January 1988
- journal article
- research article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 17 (1) , 91-94
- https://doi.org/10.1246/cl.1988.91
Abstract
α, β-Unsaturated thioesters react with silyl enol ethers to afford the corresponding Michael adducts stereoselectively in high yields by the use of a new catalyst, combined use of antimony(V) chloride and tin(II) triflate.Keywords
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