Progression of Hydroamination Catalyzed by Late Transition-Metal Complexes from Activated to Unactivated Alkenes
Author:
Affiliation:
1. Department of Chemistry, University of California, Berkeley, California 94720, United States
2. Division of Chemical Sciences, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States
Funder
U.S. Department of Energy
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
General Medicine,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.accounts.3c00141
Reference80 articles.
1. Iridium-Catalyzed Intermolecular Hydroamination of Unactivated Aliphatic Alkenes with Amides and Sulfonamides
2. Enantioselective hydroamination of unactivated terminal alkenes
3. Catalytic asymmetric addition of an amine N–H bond across internal alkenes
4. Ruthenium-Catalyzed Hydroamination of Unactivated Terminal Alkenes with Stoichiometric Amounts of Alkene and an Ammonia Surrogate by Sequential Oxidation and Reduction
5. Group‐IV Metal Complexes as Hydroamination Catalysts
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