Catalyst-Free Regioselective N2 Arylation of 1,2,3-Triazoles Using Diaryl Iodonium Salts
Author:
Affiliation:
1. Loker Hydrocarbon Research Institute and Department of Chemistry, University of Southern California, Los Angeles, California 90089-1661, United States
Funder
Loker Hydrocarbon Research Institute, University of Southern California
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b02140
Reference27 articles.
1. Medicinal attributes of 1,2,3-triazoles: Current developments
2. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes
3. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides
4. Ruthenium-Catalyzed Cycloaddition of Aryl Azides and Alkynes
5. Organocatalytic routes toward substituted 1,2,3-triazoles
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