Selective Cross-Dehydrogenative Coupling of Various Acyclic Enamides with Heteroarenes via Rh(III)-Catalyzed C–H Activation
Author:
Affiliation:
1. College of Chemistry, Nanchang University, Nanchang, Jiangxi 330031, China
2. Department of Chemistry & Chemical Engineering, Gannan Normal University, Ganzhou 341000, China
Funder
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c01786
Reference56 articles.
1. Advancing the Logic of Chemical Synthesis: C−H Activation as Strategic and Tactical Disconnections for C−C Bond Construction
2. Metal-free, atom and redox-economical construction of C–C bonds enabled by oligofluorene-containing hypercrosslinked polymers
3. Carbon–Carbon Bond Forming Reactions via Photogenerated Intermediates
4. Recent advances in the transition metal-catalyzed twofold oxidative C–H bond activation strategy for C–C and C–N bond formation
5. Catalytic Dehydrogenative Cross-Coupling: Forming Carbon−Carbon Bonds by Oxidizing Two Carbon−Hydrogen Bonds
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1. Rhodium(III)-Catalyzed Switchable β-C(sp2)–H Alkenylation and Alkylation of Acyclic Enamides with Allyl Alcohols;Organic Letters;2024-04-19
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