摘要
The first HFIP-promoted catalyst-free cascade reactions for the synthesis of biologically relevant 3,3-di(indolyl)indolin-2-ones(27 examples,up to 98% yield) from readily available indoles and isatin derivatives are described.This protocol shows well tolerance of different functional groups and features mild reaction conditions such as short reaction time(~1 h),no usage of catalyst,easy operation and product isolation.Of particular intere st is the formation of two C-C bonds and one all-carbon quaternary center.This protocol could serve as an alternative strategy to synthesize biologically important 3,3-di(indolyl)indolin-2-ones for biological testing.
基金
supported by the National Natural Science Foundation of China(Nos.81773562,81703326 and 81973177)
The Open Project of State Key Laboratory of Natural Medicines(No.SKLNMKF202005)
China Postdoctoral Science Foundation(Nos.2018M630840 and 2019T120641)。