Direct aminosulfonylation of electron-rich (hetero)arenes utilizing <i>tert</i>-butyl chlorosulfonylcarbamate and diisopropylethylamine

Using in situ generated tert -butyl sulfonylcarbamate from tert -butyl chlorosulfonylcarbamate and diisopropylethylamine, a catalyst-free, mild aminosulfonylation of electron-rich (hetero)arenes was reported.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2024-11-19
DOI
https://doi.org/10.1039/d4qo01731e
Citations
1
Primary Topic
Chemical Synthesis and Reactions
Type
article
Field-Weighted Citation Impact
0.25
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article

Direct aminosulfonylation of electron-rich (hetero)arenes utilizing tert-butyl chlorosulfonylcarbamate and diisopropylethylamine

Xiaofei Zhang, Yuanchen Zhong, Min Jiang, Chunhao Yang et al.
1 citations
Organic Chemistry Frontiers
Chemical Synthesis and Reactions
0.25
article

Direct aminosulfonylation of electron-rich (hetero)arenes utilizing tert-butyl chlorosulfonylcarbamate and diisopropylethylamine

Xiaofei Zhang, Yuanchen Zhong, Min Jiang, Chunhao Yang, Jiangtao Tan, Qian He, Zhen Zhuang
article en
1 citations

Abstract

Using in situ generated tert -butyl sulfonylcarbamate from tert -butyl chlorosulfonylcarbamate and diisopropylethylamine, a catalyst-free, mild aminosulfonylation of electron-rich (hetero)arenes was reported.

Organic Chemistry FrontiersVol. 12(2)
Chinese Academy of Sciences (CN), Ruijin Hospital (CN), Shanghai Institute of Materia Medica (CN), University of Chinese Academy of Sciences (CN)
Openalex Percentile: Top 46%
Chemical Synthesis and Reactions
0.25
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