摘要

Computational studies suggested that the B(C6F5)(3)-catalyzed synthesis of N-arylpyrrolidines from arylamines and cyclic ethers was achieved via two consecutive C-O bond activation steps by the generation of a frustrated Lewis pair. The formation of the Lewis acid-base adduct between B(C6F5)(3) and THF was crucial in the ring opening of THF while the existence of FLP was also indispensable in the cyclization process.