Reverse Brook rearrangement of 2-alkynyl trialkylsilyl ether. Synthesis of optically active (1-hydroxy-2-alkynyl)trialkylsilane
- 19 August 2000
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 41 (34) , 6589-6592
- https://doi.org/10.1016/s0040-4039(00)01086-8
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Syntheses of optically active 2-substituted cyclopropanecar☐ylic acids from chiral α-hydroxysilane derivativesTetrahedron Letters, 1998
- Asymmetric syntheses with chiral oxazaborolidinesTetrahedron: Asymmetry, 1992
- Practical and Useful Methods for the Enantioselective Reduction of Unsymmetrical KetonesSynthesis, 1992
- Synthesis of (.alpha.-hydroxyalkyl)silanes from formyltrimethylsilane. A new route to acetylenic acylsilanesThe Journal of Organic Chemistry, 1988
- Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implicationsJournal of the American Chemical Society, 1987
- Silyl ketone chemistry. Preparation and reactions of silyl allenol ethers. Diels-Alder reaction of siloxy vinylallenes leading to sesquiterpenesJournal of the American Chemical Society, 1986
- A practical and efficient synthesis of .alpha.,.beta.-unsaturated acylsilanesThe Journal of Organic Chemistry, 1985
- Base-induced rearrangement of 1-trimethylsilylpropargyl alcohol. Generation of lithiated trimethylsiloxyallenes and their reactionsTetrahedron Letters, 1980
- Silyl ketone chemistry. Preparation of siloxyallenyl- and -allyllithium reagentsJournal of the American Chemical Society, 1980
- Molecular rearrangements of organosilicon compoundsAccounts of Chemical Research, 1974