REACTION OF ENOLATES OF ACYLTRIMETHYLSILANES WITH ALDEHYDES. CANNIZZARO TYPE OXIDATION-REDUCTION REACTION WITH A TRIMETHYLSILYLCARBONYL GROUP
- 5 May 1980
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 9 (5) , 525-528
- https://doi.org/10.1246/cl.1980.525
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Silicon in organic synthesisChemical Society Reviews, 1978
- Titanium Tetrachloride in Organic Synthesis [New synthetic methods (21)]Angewandte Chemie International Edition in English, 1977
- An effective preparative method of .alpha.,.beta.-unsaturated aldehydes via .beta.-alkoxyacylsilanesJournal of the American Chemical Society, 1977
- Reactions of lithium alkoxide of 1,1-bis(trimethylsilyl)alkan-1-ol with benzophenone. A novel way to silyl enol ether of acylsilaneJournal of the American Chemical Society, 1977
- Stereoselection in the aldol condensationJournal of the American Chemical Society, 1977
- New anionic rearrangements. XVII. 1,2-Anionic rearrangements from oxygen to carbon in benzyloxyorganosilanes and benzyloxyorganogermanesJournal of the American Chemical Society, 1974
- Molecular rearrangements of organosilicon compoundsAccounts of Chemical Research, 1974
- The Spectral and Chemical Properties of α-Silyl KetonesJournal of the American Chemical Society, 1960