Efficient, mild synthesis of N-unsubstituted 1,2,3-triazoles from methanolysis of 1-sulfonyl-1,2,3-triazoles
Author:
Affiliation:
1. Centro Conjunto de Investigación en Química Sustentable UAEM-UNAM, Toluca, Estado de México, Mexico
Funder
CONACYT
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397911.2018.1484485
Reference39 articles.
1. The copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC) “click” reaction and its applications. An overview
2. Cu-Catalyzed Azide−Alkyne Cycloaddition
3. The growing applications of click chemistry
4. Cu I ‐Catalyzed Alkyne–Azide “Click” Cycloadditions from a Mechanistic and Synthetic Perspective
5. The Preparation of 1,2,3-Triazole1
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2. Azide-free cyclization reaction access to 4-aryl-NH-1,2,3-triazoles: P-toluenesulfonyl hydrazide and sulfamic acid as nitrogen sources;Organic & Biomolecular Chemistry;2024
3. Synthesis, crystal structure and theoretical studies of 1-sulfonyl-1,2,3-triazole derivatives;Journal of Molecular Structure;2023-03
4. Cycloaddition of N-sulfonyl and N-sulfamoyl azides with alkynes in aqueous media for the selective synthesis of 1,2,3-triazoles;Green Chemistry;2022
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