Straightforward and fast access to electrochemical synthesis of selective brominated <i>N</i> -aryl glycine amides

Herein, we report an electrochemical selective bromination of glycine derivatives with tert -butyl bromide.This operationally convenient methodology could enable rapid library generation of brominated or dibrominated N -aryl glycine derivatives.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-11-10
DOI
https://doi.org/10.1039/d5qo01430a
Citations
1
Primary Topic
Vanadium and Halogenation Chemistry
Type
article
Field-Weighted Citation Impact
0.54
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article

Straightforward and fast access to electrochemical synthesis of selective brominated N -aryl glycine amides

Ai‐Fang Wang, Min Wang, Xinyi Huang, Donghao Wang et al.
1 citations
Organic Chemistry Frontiers
Vanadium and Halogenation Chemistry
0.54
article

Straightforward and fast access to electrochemical synthesis of selective brominated N -aryl glycine amides

Ai‐Fang Wang, Min Wang, Xinyi Huang, Donghao Wang, Jiabin Shen, Zimei Zhong, Yiwang Chen
article en
1 citations

Abstract

Herein, we report an electrochemical selective bromination of glycine derivatives with tert -butyl bromide.This operationally convenient methodology could enable rapid library generation of brominated or dibrominated N -aryl glycine derivatives.

Organic Chemistry FrontiersVol. 13(2)
Hangzhou Normal University (CN), Zhejiang Shuren University (CN)
Openalex Percentile: Top 29%
Vanadium and Halogenation Chemistry
0.54
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