Enantioselective and Diastereodivergent Allylation of Propargylic C–H Bonds
Author:
Affiliation:
1. Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania15260, United States
2. School of Chemistry & Chemical Engineering, Yangzhou University, Yangzhou, Jiangsu225002, China
Funder
University of Pittsburgh
American Chemical Society Petroleum Research Fund
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.2c07297
Reference123 articles.
1. Enantioselective C(sp 3 )‒H bond activation by chiral transition metal catalysts
2. Transition-Metal-Catalyzed, Coordination-Assisted Functionalization of Nonactivated C(sp3)–H Bonds
3. Radical Enantioselective C(sp3 )−H Functionalization
4. Catalytic enantioselective C(sp3)–H functionalization involving radical intermediates
5. Catalytic Enantioselective Functionalizations of C–H Bonds by Chiral Iridium Complexes
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