Discover the magic of the 92-86-4

Computed Properties of C12H8Br2. About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Xiong, BJ; Wang, T; Sun, HT; Li, Y; Kramer, S; Cheng, GJ; Lian, Z or concate me.

Computed Properties of C12H8Br2. I found the field of Chemistry very interesting. Saw the article Nickel-Catalyzed Cross-Electrophile Coupling Reactions for the Synthesis of gem-Difluorovinyl Arenes published in 2020, Reprint Addresses Lian, Z (corresponding author), Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Dept Dermatol, Chengdu 610041, Peoples R China.; Lian, Z (corresponding author), Sichuan Univ, West China Hosp, Canc Ctr, Chengdu 610041, Peoples R China.; Lian, Z (corresponding author), Sichuan Univ, West China Sch Pharm, Chengdu 610041, Peoples R China.; Cheng, GJ (corresponding author), 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, S (corresponding author), Tech Univ Denmark, Dept Chem, DK-2800 Lyngby, Denmark.. The CAS is 92-86-4. Through research, I have a further understanding and discovery of 4,4′-Dibromobiphenyl.

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.

Computed Properties of C12H8Br2. About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Xiong, BJ; Wang, T; Sun, HT; Li, Y; Kramer, S; Cheng, GJ; Lian, Z or concate me.

Reference:
Benzoxazole – Wikipedia,
,Benzoxazole | C7H5NO – PubChem