Notable Coordination Effects of 2-Pyridinesulfonamides Leading to Efficient Aziridination and Selective Aziridine Ring Opening

We have developed, on the basis of a chelation-strategy, an efficient copper-catalyzed aziridination protocol with the use of 5-methyl-2-pyridinesulfonamide and PhI(OAc)2. The reaction proceeds smoothly under mild conditions to give aziridines in moderate to good yields in the
absence of external ligands or bases. The coordination-assisted approach offers the additional benefits that efficient deprotection of the
N-substituent and selective aziridine ring-opening are effectively achieved.