123273-05-2Relevant articles and documents
Synthesis of 3,3-disubstituted oxindoles by visible-light-mediated radical reactions of aryl diazonium salts with N-arylacrylamides
Fu, Weijun,Xu, Fengjuan,Fu, Yuqin,Zhu, Mei,Yu, Jiaqi,Xu, Chen,Zou, Dapeng
, p. 12202 - 12206 (2013)
A mild and efficient visible-light-mediated diarylation of N-arylacrylamides with aryl diazonium salts under mild conditions has been developed. This method provides convenient access to a variety of useful 3,3-disubstituted oxindoles by constructing two C-C bonds in one step.
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.
