Copper(I)‐Catalyzed Interrupted Click/Amidation: Regioselective Synthesis of 5‐Amide‐1,2,3‐triazoles

Comprehensive Summary A copper‐catalyzed tandem click/amidation reaction involving various alkynes, azides, and dioxazolones has been developed for the synthesis of fully substituted 5‐amide‐1,2,3‐triazoles. The key step in this reaction is the interception of the in situ ‐formed cuprate‐triazole intermediate with N ‐acyl nitrenes, which are generated from dioxazolones. The choice of precursor for the N ‐acyl nitrenes plays a crucial role in the success of the reaction. This method is characterized by a broad substrate scope, mild reaction conditions, and complete regioselectivity.

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Publication Details

Journal
Chinese Journal of Chemistry
Published
2025-08-19
DOI
https://doi.org/10.1002/cjoc.70232
Citations
7
Primary Topic
Click Chemistry and Applications
Type
article
Field-Weighted Citation Impact
6.55

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article

Copper(I)‐Catalyzed Interrupted Click/Amidation: Regioselective Synthesis of 5‐Amide‐1,2,3‐triazoles

Zhenghu Xu, Yanqin Wang, Jingyu Wang, Weiguo Wang
7 citations
Chinese Journal of Chemistry
Click Chemistry and Applications
6.55
article

Copper(I)‐Catalyzed Interrupted Click/Amidation: Regioselective Synthesis of 5‐Amide‐1,2,3‐triazoles

Zhenghu Xu, Yanqin Wang, Jingyu Wang, Weiguo Wang
article en
7 citations

Abstract

Comprehensive Summary A copper‐catalyzed tandem click/amidation reaction involving various alkynes, azides, and dioxazolones has been developed for the synthesis of fully substituted 5‐amide‐1,2,3‐triazoles. The key step in this reaction is the interception of the in situ ‐formed cuprate‐triazole intermediate with N ‐acyl nitrenes, which are generated from dioxazolones. The choice of precursor for the N ‐acyl nitrenes plays a crucial role in the success of the reaction. This method is characterized by a broad substrate scope, mild reaction conditions, and complete regioselectivity.

Chinese Journal of ChemistryVol. 43(23)
Shandong University (CN), Qufu Normal University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 3%
Click Chemistry and Applications
6.55
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