Cu-Catalyzed Site-Selective Benzylic Chlorination Enabling Net C–H Coupling with Oxidatively Sensitive Nucleophiles
Author:
Affiliation:
1. Department of Chemistry, University of Wisconsin−Madison, 1101 University Avenue, Madison, Wisconsin 53706, United States
Funder
National Institute of General Medical Sciences
National Science Foundation
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c04038
Reference39 articles.
1. Chlorine, Bromine, and Iodine;Schaumann E.,2014
2. Nickel-Catalyzed Enantioconvergent Borylation of Racemic Secondary Benzylic Electrophiles
3. Copper(I)‐Catalyzed Enantioconvergent Borylation of Racemic Benzyl Chlorides Enabled by Quadrant‐by‐Quadrant Structure Modification of Chiral Bisphosphine Ligands
4. Photocatalytic strategies for the activation of organic chlorides
5. Nickel-Catalyzed Enantioselective Reductive Cross-Coupling Reactions
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