Asymmetric Catalysis of Aldol Reactions with Chiral Lewis Bases
Author:
Affiliation:
1. Roger Adams Laboratory, Department of Chemistry, University of Illinois, Urbana, Illinois 61801
Publisher
American Chemical Society (ACS)
Subject
General Medicine,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ar960027g
Reference46 articles.
1. Exceptions to this generality include reactions which are susceptible to nucleophilic catalysis such as acylation/hydrolysis4aand the Morita−Baylis−Hilman reaction.4b(a) Bender, M. L.Mechanisms of Homogeneous Catalysis from Protons to Proteins; Wiley: New York, 1971; p 165. (b) Ciganek, E. The Catalyzed α-Hydroxyalkylation and α-Aminoalkylation of Activated Olefins (The Morita−Baylis−Hillman Reaction).Org. React.1997,51, 201−350.
2. Reactivity of penta- and hexacoordinate silicon compounds and their role as reaction intermediates
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