An article Nickel-Catalyzed Cross-Electrophile Coupling Reactions for the Synthesis of gem-Difluorovinyl Arenes WOS:000592978900045 published article about DIFLUOROMETHYL 2-PYRIDYL SULFONE; LIGHT-EMITTING-DIODES; C-O ACTIVATION; AROMATIC-ALDEHYDES; DIFLUOROALKENES; ALKENES; DIFLUOROOLEFINATION; CONSTRUCTION; AMIDATION; HALIDES in [Xiong, Baojian; Sun, Haotian; Li, Yue; Lian, Zhong] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Dept Dermatol, Chengdu 610041, Peoples R China; [Xiong, Baojian; Sun, Haotian; Li, Yue; Lian, Zhong] Sichuan Univ, West China Hosp, Canc Ctr, Chengdu 610041, Peoples R China; [Xiong, Baojian; Sun, Haotian; Li, Yue; Lian, Zhong] Sichuan Univ, West China Sch Pharm, Chengdu 610041, Peoples R China; [Wang, Ting; Cheng, Gui-Juan] Chinese Univ Hong Kong Shenzhen, Sch Life & Hlth Sci, Shenzhen Key Lab Steroid Drug Dev, Warshel Inst Computat Biol, Shenzhen 518172, Peoples R China; [Kramer, Soren] Tech Univ Denmark, Dept Chem, DK-2800 Lyngby, Denmark in 2020, Cited 82. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4. Recommanded Product: 92-86-4
A nickel-catalyzed cross-electrophile coupling reaction between (hetero)aryl bromides and 2,2-difluorovinyl tosylate is presented. This protocol provides facile incorporation of the gem-difluorovinyl moiety in organic molecules. The method features mild reaction conditions, good functional group tolerance, and excellent yields. Furthermore, mechanistic experiments and DFT studies indicate a Ni(0)/Ni(II) catalytic cycle, thus differing from the currently accepted catalytic cycle for nickel-catalyzed C(sp(2))-C(sp(2)) cross-electrophile coupling reactions.
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Reference:
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