Login / Signup

Electrochemical Aziridination by Alkene Activation Using a Sulfamate as the Nitrogen Source.

Jin LiWenhao HuangJingzhi ChenLingfeng HeXu ChengGuigen Li
Published in: Angewandte Chemie (International ed. in English) (2018)
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.
Keyphrases
  • gold nanoparticles
  • molecularly imprinted
  • ionic liquid
  • label free
  • molecular docking
  • electron transfer
  • solid phase extraction