Regioselective enolization of optically active 3-keto steroids using chiral lithium amides
- 1 January 1990
- journal article
- research article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 1 (5) , 295-298
- https://doi.org/10.1016/s0957-4166(00)86317-x
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Asymmetric deprotonation of prochiral ketones using chiral lithium amide basesTetrahedron, 1990
- Enantioselective Deprotonation of the Meso-Forms of 2,6- and 3,5-DimethylcyclohexanonesHETEROCYCLES, 1990
- Chiral products via asymmetric deprotonation of 4-tert-butylcyclohexanone using chiral lithium amide basesTetrahedron Letters, 1989
- Enolization of 2-decalonesThe Journal of Organic Chemistry, 1988
- Enantioselective deprotonation by chiral lithium amide bases: asymmetric synthesis of trimethylsilyl enol ethers from 4-alkylcyclohexanonesJournal of the American Chemical Society, 1986
- Highly selective, kinetically controlled enolate formation using lithium dialkylamides in the presence of trimethylchlorosilaneTetrahedron Letters, 1984
- Silyl Enol Ethers in Synthesis - Part IISynthesis, 1983
- 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