Chiral Ketone-Catalyzed Asymmetric Epoxidation of 2,2-Disubstituted Vinylsilanes
- 4 September 1999
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 64 (20), 7675-7677
- https://doi.org/10.1021/jo990951z
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- A pH Study on the Chiral Ketone Catalyzed Asymmetric Epoxidation of HydroxyalkenesThe Journal of Organic Chemistry, 1998
- Vinyldisilanes as masked acylsilanesChemical Communications, 1996
- Pd-Catalyzed Coupling Reaction of Acetylenes, Iodotrimethylsilane, and Organozinc Reagents for the Stereoselective Synthesis of VinylsilanesThe Journal of Organic Chemistry, 1995
- Tandem Transformations Initiated by the Migration of a Silyl Group. Some New Synthetic Applications of SilyloxiranesSynlett, 1994
- A new iterative route to optically active polyols using .alpha.-alkoxy silanes as key intermediatesThe Journal of Organic Chemistry, 1992
- Silafunctional compounds in organic synthesis. 35. Silafunctional .alpha.,.beta.-epoxy silanes. Transformation into erythro- and threo-1,2-diol skeletons and its application to the synthesis of (.+-.)-exo-brevicominThe Journal of Organic Chemistry, 1987
- Some epoxide ring-opening reactions of αβ-epoxysilanesJournal of the Chemical Society, Perkin Transactions 1, 1981
- Silicon in Synthesis. 10. The (Trimethylsilyl)allyl Anion: A .beta.-Acyl Anion Equivalent for the Conversion of Aldehydes and Ketones into .gamma.-LactonesJournal of the American Chemical Society, 1980
- Silanes in organic synthesis. 9. Enesilylation as a method for 1,2-carbonyl migration within ketones and for conversion to 1,2-transposed allylic alcoholsThe Journal of Organic Chemistry, 1980
- Organosilicon compounds with functional groups proximate to silicon. Feasible route to 1,2-epoxyalkyllithium reagents via the lithiation of epoxyethylsilanesJournal of the American Chemical Society, 1976