Highly 1,4-Syn Diastereoselective, Phosphoramide-Catalyzed Aldol Additions of Chiral Methyl Ketone Enolates
- 24 November 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 63 (25) , 9524-9527
- https://doi.org/10.1021/jo981739i
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Asymmetric aldol additions catalyzed by chiral phosphoramides: Electronic effects of the aldehyde componentTetrahedron, 1998
- Lewis Base-Catalyzed, Asymmetric Aldol Additions of Methyl Ketone EnolatesThe Journal of Organic Chemistry, 1998
- The Chemistry of Chlorosilyl Enolates 3.: Variation of the Silyl Group and the Effect on Rate and Enantiomeric Excess of Acetate Aldol AdditionsSynlett, 1997
- The Chemistry of Trichlorosilyl Enolates. 2. Highly-Selective Asymmetric Aldol Additions of Ketone EnolatesJournal of the American Chemical Society, 1997
- Chemistry of Trichlorosilyl Enolates. 1. New Reagents for Catalytic, Asymmetric Aldol AdditionsJournal of the American Chemical Society, 1996
- Recent developments in asymmetric aldol methodologyContemporary Organic Synthesis, 1994
- 1,4-Diastereoselectivity in the aldol condensation of methyl ketonesThe Journal of Organic Chemistry, 1990
- Aldol reactions in polypropionate synthesis: High π-face selectivity of enol borinates from α-chiral methyl and ethyl ketones under substrate controlTetrahedron Letters, 1989
- Stereoselective aldol condensations via boron enolatesJournal of the American Chemical Society, 1981
- Acyclic stereoselection. 12. Double stereodifferentiation with mutual kinetic resolution. A superior class of reagents for control of Cram's rule stereoselection in synthesis of erythro-.alpha.-alkyl-.beta.-hydroxy carboxylic acids from chiral aldehydesThe Journal of Organic Chemistry, 1981