摘要
An efficient and divergent synthesis of N -arylbenzimidazoles and N -arylindazoles from arylamino oximes based on reaction conditions selection was developed. The synthesis was approached by treating oximes with BTC and the chemoselectivity was regulated by the amount of Et 3 N. This switchable N–N and N–C bond formation process features mild reaction conditions, simple execution, high chemoselectivity and broad substrate scope.
危险品化学品经营许可证(带存储)