Ni-Catalyzed Reductive Cross-Coupling of Cyclopropylamines and Other Strained Ring NHP Esters with (Hetero)Aryl Halides
Author:
Affiliation:
1. Davenport Research Laboratories, Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario M5S 3H6, Canada
2. Discovery Chemistry, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, United States
Funder
University of Toronto
Canada Foundation for Innovation
Genentech
Alfred P. Sloan Foundation
Canada Research Chairs
Natural Sciences and Engineering Research Council of Canada
Ontario Research Fund
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c03570
Reference36 articles.
1. Ni-Catalyzed Reductive Cross-Coupling of Cyclopropylamines and Other Strained Ring NHP Esters with (Hetero)Aryl Halides
2. Improving Drug Design: An Update on Recent Applications of Efficiency Metrics, Strategies for Replacing Problematic Elements, and Compounds in Nontraditional Drug Space
3. A Medicinal Chemist’s Guide to Molecular Interactions
4. The role of drug metabolizing enzymes in clearance
5. Natural-Products-Inspired Use of the gem-Dimethyl Group in Medicinal Chemistry
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