Ligand-Enabled Sequential C(sp3)–H and C(sp2)–H Diolefination Reaction via Palladium Catalyst
Author:
Affiliation:
1. Engineering Research Centre of Pharmaceutical Process Chemistry, Ministry of Education, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, People’s Republic of 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.2c02502
Reference54 articles.
1. Advances in the Chemistry of Tetrahydroquinolines
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3. Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals
4. The Essential Role of Bond Energetics in C–H Activation/Functionalization
5. N-Heterocyclic Carbene Complexes in C–H Activation Reactions
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2. Palladium(II)‐Catalyzed Nondirected Late‐Stage C(sp2)−H Deuteration of Heteroarenes Enabled Through a Multi‐Substrate Screening Approach;Angewandte Chemie International Edition;2024-06-03
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4. Palladium-Catalyzed (3 + 2) Annulation of Aromatic Acids by C(sp3)–H Olefination and Decarboxylative Cross-Coupling Reaction;Organic Letters;2024-02-09
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