The Chemistry of Trichlorosilyl Enolates. 6. Mechanistic Duality in the Lewis Base-Catalyzed Aldol Addition Reaction
- 1 December 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 120 (49) , 12990-12991
- https://doi.org/10.1021/ja982993v
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Asymmetric aldol additions catalyzed by chiral phosphoramides: Electronic effects of the aldehyde componentTetrahedron, 1998
- Enantioselective Ring Opening of Epoxides with Silicon Tetrachloride in the Presence of a Chiral Lewis BaseThe Journal of Organic Chemistry, 1998
- Catalyzed enantioselective aldol additions of latent enolate equivalentsTetrahedron: Asymmetry, 1998
- Lewis Base-Catalyzed, Asymmetric Aldol Additions of Methyl Ketone EnolatesThe Journal of Organic Chemistry, 1998
- Additive effects on ligand activated allylation of aldehydes by allyltrichlorosilaneTetrahedron Letters, 1997
- The Chemistry of Trichlorosilyl Enolates. 2. Highly-Selective Asymmetric Aldol Additions of Ketone EnolatesJournal of the American Chemical Society, 1997
- Nonlinear Effects in Asymmetric CatalysisJournal of the American Chemical Society, 1994
- Nonlinear effects in asymmetric synthesis. Examples in asymmetric oxidations and aldolization reactionsJournal of the American Chemical Society, 1986
- 190. Mechanism of substitution at a saturated carbon atom. Part XXV. Unimolecular halogen exchange between an alkyl halide and halide ions in sulphur dioxide solution; and a concluding noteJournal of the Chemical Society, 1940