Synthesis of (2-Oxoindolin-3-ylidene)methyl Acetates Involving a C−H Functionalization Process Shi Tang Peng Peng Zhi-Qiang Wang Bo-Xiao Tang Chen-Liang Deng Jin-Heng Li Ping Zhong Nai-Xing Wang 10.1021/ol8006315.s001 https://acs.figshare.com/articles/journal_contribution/Synthesis_of_2_Oxoindolin_3_ylidene_methyl_Acetates_Involving_a_C_H_Functionalization_Process/2942164 A novel palladium-catalyzed oxidative C−H functionalization protocol for the synthesis of (2-oxoindolin-3-ylidene)methyl acetates has been developed. In the presence of Pd(OAc)<sub>2</sub> and PhI(OAc)<sub>2</sub>, a variety of <i>N</i>-arylpropiolamides underwent the C−H functionalization reaction with acids to afford the corresponding (<i>E</i>)-(2-oxoindolin-3-ylidene)methyl acetates selectively in moderate to excellent yields. 2008-05-01 00:00:00 PhI presence acetate Oxoindolin Pd Functionalization acid variety oxoindolin functionalization synthesis yield oxidative Acetate Synthesi