Stereo- and regio-selective conversion of 1-trimethylsilylallylic alcohols into the silyl enol ethers catalyzed by butyllithium
- 31 December 1980
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 21 (28) , 2745-2748
- https://doi.org/10.1016/s0040-4039(00)78595-9
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Silyl ketone chemistry. A new regiospecific route to silyl enol ethersJournal of the American Chemical Society, 1979
- 1-Trimethylsilylallylic alcohols as homoenolate precursors. Stereo- and regio-specific synthesis of silyl enol ethersJournal of the Chemical Society, Chemical Communications, 1979
- Chemistry of organosilicon compounds. 106. .alpha.-Siloxyallylsilanes as homoenolate anion equivalents. A novel synthesis of .gamma.-keto aldehydesThe Journal of Organic Chemistry, 1978
- Silicon in organic synthesisChemical Society Reviews, 1978
- Allyloxycarbanions. A synthesis of 3,4-dihydroxy-1-olefins from carbonyl compoundsThe Journal of Organic Chemistry, 1976
- The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formationJournal of the American Chemical Society, 1976
- Quaternary ammonium enolates as synthetic intermediates. Trimethylsilylacetate: a new class of silylating reagent for ketones and alcoholsJournal of the American Chemical Society, 1976
- Silylierung von Carbonylverbindungen mit Trifluoromethansulfonsäure-trimethylsilylesterSynthesis, 1976
- Metalated allylic ethers as homoenolate anion equivalentsJournal of the American Chemical Society, 1974
- Allyloxy carbanions. New synthesis of aldehydes via a .beta.-acyl carbanion equivalentJournal of the American Chemical Society, 1974