Tridentate Directing Groups Stabilize 6-Membered Palladacycles in Catalytic Alkene Hydrofunctionalization
Author:
Affiliation:
1. Department of Chemistry, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, California 92037, United States
2. Department of Chemistry, University of Pittsburgh, 219 Parkman Avenue, Pittsburgh, Pennsylvania 15260, United States
Funder
Division of Chemistry
Deutscher Akademischer Austauschdienst
Division of Graduate Education
Pfizer
National Institute of General Medical Sciences
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.7b08383
Reference29 articles.
1. Substrate-directable chemical reactions
2. Directed, Regiocontrolled Hydroamination of Unactivated Alkenes via Protodepalladation
3. Catalytic, Regioselective Hydrocarbofunctionalization of Unactivated Alkenes with Diverse C–H Nucleophiles
4. Palladium-Catalyzed Intramolecular Addition of 1,3-Diones to Unactivated Olefins
5. Recent progress in transition metal catalysed hydrofunctionalisation of less activated olefins
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