Non-Innocent Role of Sacrificial Anodes in Electrochemical Nickel-Catalyzed C(sp2)-C(sp3) Cross-Electrophile Coupling

被引:4
|
作者
Cardinale, Luana [1 ]
Beutner, Gregory L. [2 ]
Bemis, Christopher Y. [2 ]
Weix, Daniel J. [1 ]
Stahl, Shannon S. [1 ]
机构
[1] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[2] Bristol Myers Squibb, Chem Proc Dev, New Brunswick, NJ 08903 USA
基金
美国国家科学基金会;
关键词
ARYL HALIDES; HETEROARYL HALIDES; ELECTROREDUCTION; POLYMERIZATION; BROMIDES; COMPLEX;
D O I
10.1021/jacs.4c10979
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Sacrificial anodes composed of inexpensive metals such as Zn, Fe, and Mg are widely used to support electrochemical nickel-catalyzed cross-electrophile coupling (XEC) reactions, in addition to other reductive electrochemical transformations. Such anodes are appealing because they provide a stable counter-electrode potential and typically avoid interference with the reductive chemistry. The present study outlines the development of an electrochemical Ni-catalyzed XEC reaction that streamlines access to a key pharmaceutical intermediate. Metal ions derived from sacrificial anode oxidation, however, directly contribute to homocoupling and proto-dehalogenation side products that are commonly formed in chemical and electrochemical Ni-catalyzed XEC reactions. Use of a divided cell limits interference by the anode-derived metal ions and supports a high product yield with negligible side product formation, introducing a strategy to overcome one of the main limitations of Ni-catalyzed XEC.
引用
收藏
页码:32249 / 32254
页数:6
相关论文
共 50 条
  • [1] Nickel-Catalyzed Electrochemical Cross-Electrophile C(sp2)-C(sp3) Coupling via a NiII Aryl Amido Intermediate
    Luo, Jian
    Davenport, Michael T.
    Ess, Daniel H.
    Liu, T. Leo
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2024, 63 (38)
  • [2] Photoinduced Nickel-Catalyzed Deaminative Cross-Electrophile Coupling for C(sp2)-C(sp3) and C(sp3)-C(sp3) Bond Formation
    Yang, Tao
    Wei, Yi
    Koh, Ming Joo
    ACS CATALYSIS, 2021, 11 (11): : 6519 - 6525
  • [3] Nickel-Catalyzed C-I-Selective C(sp2)-C(sp3) Cross-Electrophile Coupling of Bromo(iodo)arenes with Alkyl Bromides
    Ying, Xiaoyuan
    Li, Yuxi
    Li, Luyang
    Li, Chao
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2023, 62 (26)
  • [4] Nickel-Catalyzed C(sp3)-C(sp3) Cross-Electrophile Coupling of InSitu Generated NHP Esters with Unactivated Alkyl Bromides
    Kang, Kai
    Weix, Daniel J.
    ORGANIC LETTERS, 2022, 24 (15) : 2853 - 2857
  • [5] Nickel-Catalyzed Enantioselective C(sp3)-C(sp3) Cross-Electrophile Coupling of N-Sulfonyl Styrenyl Aziridines with Alkyl Bromides
    Lan, Yun
    Han, Qiaoying
    Liao, Pingyong
    Chen, Ruijia
    Fan, Fei
    Zhao, Xuejun
    Liu, Wenbin
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2024, 146 (37) : 25426 - 25432
  • [6] Nickel-Catalyzed Cross-Electrophile C(sp3)-Si Coupling of Unactivated Alkyl Bromides with Vinyl Chlorosilanes
    Duan, Jicheng
    Wang, Yuquan
    Qi, Liangliang
    Guo, Peng
    Pang, Xiaobo
    Shu, Xing-Zhong
    ORGANIC LETTERS, 2021, 23 (20) : 7855 - 7859
  • [7] Di(2-picolyl)amines as Modular and Robust Ligands for Nickel- Catalyzed C(sp2)-C(sp3) Cross-Electrophile Coupling
    Rago, Alexander J.
    Vasilopoulos, Aristidis
    Dombrowski, Amanda W.
    Wang, Ying
    ORGANIC LETTERS, 2022, 24 (46) : 8487 - 8492
  • [8] Micelle enabled C(sp2)-C(sp3) cross-electrophile coupling in water via synergistic nickel and copper catalysis
    Ye, Ning
    Wu, Bin
    Zhao, Kangming
    Ge, Xiaobin
    Zheng, Yu
    Shen, Xiaodong
    Shi, Lei
    Cortes-Clerget, Margery
    Regnier, Morgan Louis
    Parmentier, Michael
    Gallou, Fabrice
    CHEMICAL COMMUNICATIONS, 2021, 57 (62) : 7629 - 7632
  • [9] Nickel-Catalyzed Electrochemical C(sp3)-C(sp2) Cross-Coupling Reactions of Benzyl Trifluoroborate and Organic Halides**
    Luo, Jian
    Hu, Bo
    Wu, Wenda
    Hu, Maowei
    Liu, T. Leo
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2021, 60 (11) : 6107 - 6116
  • [10] Electrochemical Ni-Catalyzed Decarboxylative C(sp3)-N Cross-Electrophile Coupling
    Cai, Yue-Ming
    Liu, Xiao-Ting
    Xu, Lin-Lin
    Shang, Ming
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2024, 63 (12)