β,γ-Vicinal Dicarbofunctionalization of Alkenyl Carbonyl Compounds via Directed Nucleopalladation
Author:
Affiliation:
1. Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States
Funder
Pfizer
Scripps Research Institute
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.6b09170
Reference29 articles.
1. Organocopper Conjugate Addition-Enolate Trapping Reactions
2. Tandem Vicinal Difunctionalization: β-Addition to α,β-Unsaturated Carbonyl Substrates Followed by α-Functionalization
3. Syntheses of Polycyclic Natural Products Employing the Intramolecular Double Michael Reaction
4. Directed, Regiocontrolled Hydroamination of Unactivated Alkenes via Protodepalladation
5. Catalytic, Regioselective Hydrocarbofunctionalization of Unactivated Alkenes with Diverse C–H Nucleophiles
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