Synthesis of α-Aryl Secondary Amides via Nickel-Catalyzed Reductive Coupling of Redox-Active Esters
Author:
Affiliation:
1. Davenport Research Laboratories, Department of Chemistry, University of Toronto, Toronto, Ontario M5S 3H6, Canada
2. Department of Process Research and Development, Merck & Co., Inc., Rahway, New Jersey 07065, United States
Funder
University of Toronto
Merck
Canada Foundation for Innovation
Canada Research Chairs
Government of Canada
Government of Ontario
Ontario Ministry of Research, Innovation and Science
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c00918
Reference47 articles.
1. Transition Metal-Catalyzed Direct Arylation of Substrates with Activated sp3-Hybridized C−H Bonds and Some of Their Synthetic Equivalents with Aryl Halides and Pseudohalides
2. Palladium-Catalyzed α-Arylation of Carbonyl Compounds and Nitriles
3. Metal-Catalyzed α-Arylation of Carbonyl and Related Molecules: Novel Trends in CC Bond Formation by CH Bond Functionalization
4. Metal-catalysed approaches to amide bond formation
5. Rethinking amide bond synthesis
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