67031-68-9Relevant articles and documents
Highly regioselective ring opening of a common N,N-dialkylaziridinium ion by carboxylic acids
Hernández, Ulises,Velasco, Manuel,Vázquez, Jaime,Terán, Joel L.,Gnecco, Dino,Orea, María L.,Aparicio, David M.,Juárez, Jorge R.
, p. 219 - 232 (2018)
A variety of optically active amino esters were synthesized via ring-opening reaction of (R)-1-phenyl-3-Azaspiro[2.5]octan-3-ium ion derived from (R)-2-phenyl-2-(piperidin-1-yl)ethan-1-ol in a highly regioselective manner. Ring-opening reaction with carboxylates series generated in situ proceeded smoothly and with excellent yields (85-98%).