摘要
A new route to synthesize β-iodo amines from sulfonyl aziridines and iodine was developed in the presence of PPh3. This ring-opening reaction was an efficient and simple process to give fl-iodo amines in excellent yields with high chemoselectivity.
A new route to synthesize β-iodo amines from sulfonyl aziridines and iodine was developed in the presence of PPh3. This ring-opening reaction was an efficient and simple process to give fl-iodo amines in excellent yields with high chemoselectivity.
基金
We express our appreciation to the Anhui Provincial Natural Science Foundation