Characterization and Reactivity of Copper(II) and Copper(III) σ-Aryl Intermediates in Aminoquinoline-Directed C–H Functionalization
Author:
Affiliation:
1. Department of Chemistry, University of Michigan, 930 N. University Avenue, Ann Arbor, Michigan 48109, United States
2. Department of Chemistry, Reed College, 3203 Woodstock Boulevard, Portland, Oregon 97202, United States
Funder
Division of Chemistry
Reed College
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.3c00914
Reference67 articles.
1. Highly Regioselective Arylation of sp3 C−H Bonds Catalyzed by Palladium Acetate
2. 3d Transition Metals for C–H Activation
3. Copper-Catalyzed or -Mediated CH Bond Functionalizations Assisted by Bidentate Directing Groups
4. Recent advances in copper-mediated chelation-assisted functionalization of unactivated C–H bonds
5. Copper-Mediated Decarboxylative Coupling of Benzamides with ortho -Nitrobenzoic Acids by Directed C−H Cleavage
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