Highly 1,4-Syn Diastereoselective, Phosphoramide-Catalyzed Aldol Additions of Chiral Methyl Ketone Enolates
Author:
Affiliation:
1. Roger Adams Laboratory, Department of Chemistry, University of Illinois, Urbana, Illinois 61801
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo981739i
Reference21 articles.
1. Chemistry of Trichlorosilyl Enolates. 1. New Reagents for Catalytic, Asymmetric Aldol Additions
2. The Chemistry of Trichlorosilyl Enolates. 2. Highly-Selective Asymmetric Aldol Additions of Ketone Enolates
3. The Chemistry of Chlorosilyl Enolates 3.: Variation of the Silyl Group and the Effect on Rate and Enantiomeric Excess of Acetate Aldol Additions
4. Lewis Base-Catalyzed, Asymmetric Aldol Additions of Methyl Ketone Enolates
5. Asymmetric aldol additions catalyzed by chiral phosphoramides: Electronic effects of the aldehyde component
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