A Mild and Efficient Method for the Syntheses and Regioselective Ring-Opening of Aziridines

Abstract

We have developed a new synthetic method for the synthesis of aziridines using Chloramine-T as an effective reagent in the presence of NH2OH center dot HCl and NaIO4. We found that the same combination of NH2OH center dot HCl and NaIO4 is also very effective for nucleophilic ring opening of aziridines.This research was funded by the Russian Science Foundation, grant number 18-19-00090