32380-61-3Relevant academic research and scientific papers
Nickel-Catalyzed Domino Heck Cyclization/Suzuki Coupling for the Synthesis of 3,3-Disubstituted Oxindoles
Li, Yuxiu,Wang, Kuai,Ping, Yuanyuan,Wang, Yifan,Kong, Wangqing
, p. 921 - 924 (2018/02/22)
The first nickel-catalyzed domino Heck cyclization/Suzuki coupling reaction for the synthesis of 3,3-disubstituted oxindoles bearing quaternary all-carbon centers is reported. A wide range of electrophiles, such as aryl iodides, bromides, triflates, and c
Copper-catalyzed oxidative electrophilic carbofunctionalization of acrylamides for the synthesis of oxindoles
Li, Xueqin,Xu, Jian,Zhang, Pengbo,Gao, Yuzhen,Wu, Ju,Tang, Guo,Zhao, Yufen
, p. 2009 - 2012 (2014/11/08)
A novel and efficient copper-catalyzed tandem oxidative cyclization of arylacrylamides with diaryliodonium salts is reported. This reaction provides a novel approach for the synthesis of oxindoles and various functional groups were well tolerated.
Copper-catalyzed bis-arylations of alkenes leading to oxindole derivatives
Shi, Liangliang,Wang, Yuyuan,Yang, Haijun,Fu, Hua
supporting information, p. 4070 - 4073 (2014/06/10)
A simple and practical copper-catalyzed approach to oxindole derivatives by copper-catalyzed bis-arylation of N-alkyl-N-phenylacrylamides with diaryliodonium triflates has been developed under mild conditions, and the method is of tolerance towards some functional groups in the substrates. This journal is the Partner Organisations 2014.
