摘要
A metal-free and efficient approach to N -arylpyrrolidines from arylamines and cyclic ethers catalyzed by hydrogen iodine is described. In this protocol, no additive is added and a wide range of N -arylpyrrolidines are synthesized with up to 99% yield. Reaction mechanism involving iodine radical is proposed.
危险品化学品经营许可证（带存储）