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Carbamoyl Anion Addition to Azirines.

Michael J KernerChristian A KuttruffMaxim ChevliakovFrederic G BuonoDonghong A GaoMariusz KrawiecCarl A BusaccaChris H SenanayakePeter WipfJonathan T Reeves
Published in: Organic letters (2021)
The addition of carbamoyl anions to azirines affords synthetically useful 2-aziridinyl amide building blocks. The reaction scope was explored with respect to both formamide and azirine, and the addition was found to be highly diastereoselective. A one-pot conversion of a ketoxime to an aziridinyl amide was demonstrated. The method was employed to incorporate an aziridine residue into a dipeptide segment.
Keyphrases
  • ionic liquid
  • electron transfer