A Highly Efficient Monophosphine Ligand for Parts per Million Levels Pd-Catalyzed Suzuki-Miyaura Coupling of (Hetero)Aryl Chlorides

被引:19
|
作者
Choy, Pui Ying [1 ,2 ,3 ]
Yuen, On Ying [1 ,2 ,3 ]
Leung, Man Pan [1 ,2 ,3 ]
Chow, Wing Kin [4 ]
Kwong, Fuk Yee [1 ,2 ,3 ,4 ]
机构
[1] Chinese Univ Hong Kong, Shenzhen Res Inst, Shenzhen Municipal Key Lab Chem Synth Med Organ M, 10 Second Yuexing Rd, Shenzhen 518507, Peoples R China
[2] Chinese Univ Hong Kong, Dept Chem, Shatin, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, State Key Lab Synthet Chem, Shatin, Hong Kong, Peoples R China
[4] Hong Kong Polytech Univ, Shenzhen Res Inst SZRI, Shenzhen 518057, Peoples R China
基金
中国国家自然科学基金;
关键词
Suzuki-Miyaura reaction; Cross-coupling; Homogeneous catalysis; Palladium; Phosphine ligands; ARYL CHLORIDES; C-C; PALLADIUM; HETEROARYL; ARYLATION; MESYLATES; HALIDES; AMINATION; BIARYLS; DESIGN;
D O I
10.1002/ejoc.202000068
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A new indolylphosphine WK-phos has been synthesized for Pd-catalyzed Suzuki-Miyaura coupling of (hetero)aryl chlorides with (alkyl)arylboronic acids. Comprising this newly developed ligand with palladium(II) acetate, the resulting catalyst system was found to be highly effective in facilitating the reaction even when the catalyst loading reaches parts per million levels (e.g. 10 ppm). These examples represent one of the lowest catalyst loadings reported to date of employing monophosphine (e.g. Ar-PCy2) for Suzuki-Miyaura reactions. The ligand geometry has also been well-characterized by single-crystal X-ray crystallography.
引用
收藏
页码:2846 / 2853
页数:8
相关论文
共 50 条
  • [1] Ferrocenyl monophosphine ligands: Synthesis and applications in the Suzuki-Miyaura coupling of aryl chlorides
    Baillie, C
    Zhang, LX
    Xiao, JL
    JOURNAL OF ORGANIC CHEMISTRY, 2004, 69 (22): : 7779 - 7782
  • [2] TXPhos: a highly stable and efficient ligand designed for ppm level Pd-catalyzed Suzuki-Miyaura coupling in water
    Zhang, Lei
    Hu, Wenbo
    Li, Heng
    Shi, Jicheng
    Yuan, Bingxin
    GREEN CHEMISTRY, 2023, 25 (17) : 6635 - 6641
  • [3] Efficient Suzuki-Miyaura Coupling of Deactivated Aryl Chlorides Catalyzed by an Oxime Palladacycle
    Alonso, Diego A.
    Civicos, J. F.
    Najera, Carmen
    SYNLETT, 2009, (18) : 3011 - 3015
  • [4] Highly efficient and reusable supported Pd catalysts for Suzuki-Miyaura reactions of aryl chlorides
    Schweizer, Stephane
    Becht, Jean-Michel
    Le Drian, Claude
    ORGANIC LETTERS, 2007, 9 (19) : 3777 - 3780
  • [5] Monooxychlorophosphine as a novel and efficient ligand for palladium-catalyzed suzuki-miyaura cross-coupling of aryl chlorides
    Mai, Wenpeng
    Lv, Guanghua
    Gao, Lianxun
    SYNLETT, 2007, (14) : 2247 - 2251
  • [6] Activity and Recyclability Improvement Through Adjusting the Tethering Strategy for Pd-Catalyzed Suzuki-Miyaura Coupling Reaction of Aryl Chlorides
    Zhang, Jing-Fan
    Wang, Mingda
    Guo, Xu-Qing
    Liu, Shu
    Cao, Hui
    Li, Yuan-Long
    Zhou, Quan
    Hou, Xiu-Feng
    CATALYSIS LETTERS, 2015, 145 (12) : 2001 - 2009
  • [7] A Highly Active Catalyst System for Suzuki-Miyaura Coupling of Aryl Chlorides
    Liu, Guiyan
    Han, Fangwai
    Liu, Chengxin
    Wu, Hongli
    Zeng, Yongfei
    Zhu, Rongjiao
    Yu, Xia
    Rao, Shuang
    Huang, Genping
    Wang, Jianhui
    ORGANOMETALLICS, 2019, 38 (07) : 1459 - 1467
  • [8] Efficient catalyst for the Suzuki-Miyaura coupling of potassium aryl trifluoroborates with aryl chlorides
    Barder, TE
    Buchwald, SL
    ORGANIC LETTERS, 2004, 6 (16) : 2649 - 2652
  • [9] N-methyliminodiacetic acid as a simple and highly efficient ligand for palladium-catalyzed Suzuki-Miyaura cross-coupling of aryl chlorides
    Qi, Liang
    Zhou, Xiuling
    Li, Xiaogang
    Li, Wei
    Lv, Meiyun
    Guo, Mengping
    APPLIED ORGANOMETALLIC CHEMISTRY, 2015, 29 (04) : 244 - 246
  • [10] Pd-Catalyzed Suzuki-Miyaura Cross-Coupling of Pentafluorophenyl Esters
    Buchspies, Jonathan
    Pyle, Daniel J.
    He, Huixin
    Szostak, Michal
    MOLECULES, 2018, 23 (12):