Regioselectively Electrochemical Synthesis of N2-Selective C–H Amination of Ethers with N-Tosyl 1,2,3-Triazole via Triazole Radical Cation
Author:
Affiliation:
1. Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, China
Funder
East China Normal University
Fundamental Research Funds for the Central Universities
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.3c01896
Reference42 articles.
1. Click Chemistry: 1,2,3-Triazoles as Pharmacophores
2. 1,2,3-Triazole-containing hybrids as leads in medicinal chemistry: A recent overview
3. 1,2,3-Triazoles: Lead Molecules For Promising Drugs: A Review
4. Evaluation of Amide Bioisosteres Leading to 1,2,3-Triazole Containing Compounds as GPR88 Agonists: Design, Synthesis, and Structure–Activity Relationship Studies
5. Design of Radiolabeled Analogs of Minigastrin by Multiple Amide-to-Triazole Substitutions
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1. Synergistic Organoboron/Palladium Cocatalyzed Dehydrative Couplings of Azoles with Allylic Alcohols: A Combined Experimental and Computational Mechanistic Investigation;ACS Catalysis;2024-04-16
2. Iodide ion-enabled highly regioselective α-C(sp3)–H triazolization of ethers with N-sulfonyl-1,2,3-triazoles;New Journal of Chemistry;2024
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