Direct Asymmetric Michael Addition to Nitroalkenes: Vinylogous Nucleophilicity under Dinuclear Zinc Catalysis
Author:
Affiliation:
1. Department of Chemistry, Stanford University, Stanford, California 94305-5080
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja809723u
Reference31 articles.
1. Recent Advances in Asymmetric Organocatalytic 1,4‐Conjugate Additions
2. Recent Advances in Catalytic Enantioselective Michael Additions
3. Recent Advances in Metal-Catalyzed Asymmetric Conjugate Additions
4. Development of a Catalytic Enantioselective Conjugate Addition of 1,3-Dicarbonyl Compounds to Nitroalkenes for the Synthesis of Endothelin-A Antagonist ABT-546. Scope, Mechanism, and Further Application to the Synthesis of the Antidepressant Rolipram
5. Catalytic Enantioselective Michael Addition of 1,3-Dicarbonyl Compounds to Nitroalkenes Catalyzed by Well-Defined Chiral Ru Amido Complexes
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