Electrochemical C–H Azidation and Diazidation of Anilines for the Synthesis of Aryl Azides and Diazides

The increasing importance and need in many aspects have driven the rapid development of synthetic studies toward aryl azides. In this paper, electrochemical C-H azidation and diazidation of anilines have been developed using TMSN<sub>3</sub> as an azide source. A range of functional groups can be tolerated under the optimized reaction conditions.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-08-23
DOI
https://doi.org/10.1021/acs.joc.4c01265
Citations
1
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.25

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article

Electrochemical C–H Azidation and Diazidation of Anilines for the Synthesis of Aryl Azides and Diazides

Renhua Fan, Qiuqin He, Juan Chen, Xinliang Feng
1 citations
The Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
0.25
article

Electrochemical C–H Azidation and Diazidation of Anilines for the Synthesis of Aryl Azides and Diazides

Renhua Fan, Qiuqin He, Juan Chen, Xinliang Feng
article en
1 citations

Abstract

The increasing importance and need in many aspects have driven the rapid development of synthetic studies toward aryl azides. In this paper, electrochemical C-H azidation and diazidation of anilines have been developed using TMSN<sub>3</sub> as an azide source. A range of functional groups can be tolerated under the optimized reaction conditions.

The Journal of Organic ChemistryVol. 89(17)
Fudan University (CN), Xinjiang University of Science and Technology, Xinjiang University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 49%
Sulfur-Based Synthesis Techniques
0.25
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