The Reaction of Acetals with Silyl Enol Ethers Promoted by the Combination of Tin(II) Chloride and Organic Halide. Novel and Convenient Synthesis of α,β-Unsaturated Ketones
- 1 December 1990
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 63 (12) , 3716-3718
- https://doi.org/10.1246/bcsj.63.3716
Abstract
No abstract availableThis publication has 2 references indexed in Scilit:
- Trialkylsilyl triflates. 5. A stereoselective aldol-type condensation of enol silyl ethers and acetals catalyzed by trimethylsilyl trifluoromethanesulfonateJournal of the American Chemical Society, 1980
- An effective preparative method of .alpha.,.beta.-unsaturated aldehydes via .beta.-alkoxyacylsilanesJournal of the American Chemical Society, 1977