Guobin Ma
Shanghai University
34 Papers
269 Citations
Guobin Ma is an academic researcher from Shanghai University. The author has contributed to research in topics: Chemistry & Catalysis. The author has an hindex of 11, co-authored 31 publications.
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Papers
Ni-Catalyzed Reductive Coupling of Electron-Rich Aryl Iodides with Tertiary Alkyl Halides
Xuan Wang,Guobin Ma,Yu Peng,Chloe E. Pitsch,Brenda J. Moll,Thu D. Ly,Xiaotai Wang,Hegui Gong +7 more
TL;DR: This work illustrates the reductive coupling of electron-rich aryl halide with tertiary alkyl halides under Ni-catalyzed cross-electrophile coupling conditions, which offers an efficient protocol for the construction of all carbon quaternary stereogenic centers.
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Room-temperature Cu(II)-catalyzed aromatic C–H azidation for the synthesis of ortho-azido anilines with excellent regioselectivity
TL;DR: Cu(ii)-catalyzed aromatic C-H azidation with azido-benziodoxolone under mild conditions has been described, providing ortho-azidated anilines as the sole products.
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Silver-catalyzed oxidative decarboxylation of difluoroacetates: efficient access to C–CF2 bond formation
Wen Wan,Guobin Ma,Jialiang Li,Yunrong Chen,Qingyang Hu,Minjie Li,Haizhen Jiang,Hongmei Deng,Jian Hao,Jian Hao +9 more
TL;DR: A mild, versatile and efficient method for the silver(I)-catalyzed oxidative decarboxylative gem-difluoromethylenation has been developed that provides a novel and efficient access to the C-CF2 bond formation.
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An efficient regioselective hydrodifluoromethylation of unactivated alkenes with TMSCF2CO2Et at ambient temperature
Guobin Ma,Wen Wan,Jialiang Li,Qingyang Hu,Haizhen Jiang,Shizheng Zhu,Jing Wang,Jian Hao,Jian Hao +8 more
TL;DR: A mild, versatile and efficient method for the regioselective hydrodifluoromethylation of unactivated alkenes has been developed.
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Highly effective copper-mediated gem-difluoromethylenation of arylboronic acids.
TL;DR: A copper-mediated gem-difluoromethylenation of aryl, heteroaryl and vinyl boronic acids with bromodifluorsized oxazole or thiazole derivatives showed an excellent functional group tolerance and wide substrate scope, providing facile access to practical application in drug discovery and development.
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