Highly regioselective generation of “thermodynamic” enolates and their direct characterization by NMR
- 31 December 1983
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 24 (13) , 1341-1344
- https://doi.org/10.1016/s0040-4039(00)81651-2
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Selective carbon-carbon bond formation via transition metal catalysis. 29. A highly regio- and stereospecific palladium-catalyzed allylation of enolates derived from ketonesThe Journal of Organic Chemistry, 1982
- A highly selective method for α-alkylation of ketones potassium enoxytrialkylboratesTetrahedron Letters, 1979
- Reactions of ketones with sodium hydride or potassium hydride in the presence of trimethylsilyl chloride. Preparation of trimethylsilyl enol ethersThe Journal of Organic Chemistry, 1978
- Structure and reactivity of alkali metal enolatesTetrahedron, 1977
- Tetrahedron report number 25Tetrahedron, 1976
- Saline hydrides and superbases in organic reactions. VII. Potassium hydride, highly active new hydride reagent. Reactivity, applications, and techniques in organic and organometallic reactionsThe Journal of Organic Chemistry, 1974
- Chemistry of carbanions. XVIII. Preparation of trimethylsilyl enol ethersThe Journal of Organic Chemistry, 1969
- Isolation of ketone enolates as trialkylsilyl ethersJournal of the American Chemical Society, 1968
- The Chemistry of Carbanions. V. The Enolates Derived from Unsymmetrical Ketones1aThe Journal of Organic Chemistry, 1963