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Updated: Feb 12, 2026

Preparation of Enantiopure Non-Activated Aziridines and Synthesis of Biemamide B, D, and epiallo-Isomuscarine
Published on: June 13, 2022
Electrochemical Aziridination by Alkene Activation Using a Sulfamate as the Nitrogen Source
Jin Li1, Wenhao Huang1, Jingzhi Chen1
1Institute of Chemistry and Biomedical Sciences, Jiangsu Key Laboratory of Advanced Organic Materials, School of Chemistry and Chemical Engineering, National Demonstration Center for Experimental Chemistry Education, Nanjing University, Nanjing, 210023, China.
Abstract:
The first direct aziridination of triaryl-substituted alkenes was achieved by means of an electrochemical process that could extend to multisubstituted styrenes. Specifically, hexafluoroisopropanol sulfamate was used as a nucleophilic nitrogen source. Mechanistic experiments suggest that this electrochemical process proceeds by stepwise formation of two C-N bonds through reactions between cationic carbon species and the sulfamate.
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