Photoinduced Copper‐Catalyzed Radical Ring‐Opening Azidation of Cyclic Oxime Esters

A photoinduced copper‐catalyzed radical ring‐opening azidation of cyclic oxime esters has been developed for the synthesis of valuable γ ‐azido alkylnitriles. Furthermore, a one‐pot sequential strategy integrating this ring‐opening azidation with copper‐catalyzed azide–alkyne cycloaddition is successfully implemented, enabling the direct construction of 1,2,3‐triazole derivatives in a single operation.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-09-22
DOI
https://doi.org/10.1002/adsc.70133
Primary Topic
Click Chemistry and Applications
Type
article
Field-Weighted Citation Impact
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article

Photoinduced Copper‐Catalyzed Radical Ring‐Opening Azidation of Cyclic Oxime Esters

Tao Zou, Libo Yang, Xiaoshuang Zhou, Jing Li et al.
Advanced Synthesis & Catalysis
Click Chemistry and Applications
article

Photoinduced Copper‐Catalyzed Radical Ring‐Opening Azidation of Cyclic Oxime Esters

Tao Zou, Libo Yang, Xiaoshuang Zhou, Jing Li, Ya‐Min Li, Yuan Qu, Jia Hu
article en

Abstract

A photoinduced copper‐catalyzed radical ring‐opening azidation of cyclic oxime esters has been developed for the synthesis of valuable γ ‐azido alkylnitriles. Furthermore, a one‐pot sequential strategy integrating this ring‐opening azidation with copper‐catalyzed azide–alkyne cycloaddition is successfully implemented, enabling the direct construction of 1,2,3‐triazole derivatives in a single operation.

Advanced Synthesis & CatalysisVol. 367(22)
Kunming University of Science and Technology (CN), Fuyang Normal University (CN)
Openalex Percentile: Top 81%
Click Chemistry and Applications
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