Electronic Directing Group Modification for Improved Ni(II)-Mediated C(sp3)–H Activation: A Hammett Investigation of 8-Aminoquinoline
Author:
Affiliation:
1. Department of Chemistry, University of British Columbia, Vancouver, British Columbia V6T1Z1, Canada
2. Department of Chemistry, University of Calgary, Calgary, Alberta T2N1N4, Canada
Funder
University of Calgary
Natural Sciences and Engineering Research Council of Canada
University of British Columbia
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.organomet.3c00199
Reference53 articles.
1. Palladium-Catalyzed Transformations of Alkyl C–H Bonds
2. CH Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals
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5. Late-stage C–H functionalization offers new opportunities in drug discovery
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1. Speciation and Reactivity of Mono- and Binuclear Ni Intermediates in Aminoquinoline-Directed C–H Arylation and Benzylation;Journal of the American Chemical Society;2024-06-20
2. Reactions of cyclonickelated complexes with hydroxylamines and TEMPO˙: isolation of new TEMPOH adducts of Ni(ii) and their reactivities with nucleophiles and oxidants;Dalton Transactions;2024
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