Investigating the mechanism of Ni-mediated trifluoromethylthiolation of aryl halides using AgSCF3
Author:
Affiliation:
1. Department of Chemistry, The University of British Columbia, Vancouver, BC, V6T 1Z1, Canada
2. Department of Chemistry, University of Calgary, Calgary, AB, T2N 1N4, Canada
Abstract
Funder
University of British Columbia
University of Calgary
Natural Sciences and Engineering Research Council of Canada
Publisher
Royal Society of Chemistry (RSC)
Subject
Inorganic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2023/DT/D2DT03758K
Reference49 articles.
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4. Decarbonylative Cross-Couplings: Nickel Catalyzed Functional Group Interconversion Strategies for the Construction of Complex Organic Molecules
5. Designing Pd and Ni Catalysts for Cross-Coupling Reactions by Minimizing Off-Cycle Species
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1. Electrochemical Trifluoromethylthiolation/Cyclization of N-Arylacrylamides with AgSCF3: Access to SCF3-Containing Oxindoles;The Journal of Organic Chemistry;2024-08-19
2. AgSCF3 Radical Addition Based on an Oxidant-Free α,β-Amide (Trifluoromethyl)sulfanylation Reaction;Synlett;2024-04-18
3. Copper-promoted indirect trifluoromethylthiolation of sulfuryl chloride with TMSCF3: facile access to trifluoromethyl thioethers;New Journal of Chemistry;2023
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