A Practical Heterogeneous Catalyst for the Suzuki, Sonogashira, and Stille Coupling Reactions of Unreactive Aryl Chlorides

被引:310
|
作者
Jin, Myung-Jong [1 ]
Lee, Dong-Hwan [1 ]
机构
[1] Inha Univ, Dept Sci & Chem Engn, Inchon 402751, South Korea
基金
新加坡国家研究基金会;
关键词
aryl chlorides; cross-coupling; magnetic properties; palladium; supported catalysts; SUPPORTED PALLADIUM CATALYSTS; ENCAPSULATED PD NANOPARTICLES; N-HETEROCYCLIC CARBENES; RECYCLABLE CATALYST; COPPER-FREE; MAGNETIC NANOPARTICLES; MIYAURA REACTIONS; HECK REACTIONS; EFFICIENT; CARBON;
D O I
10.1002/anie.200905626
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
(Chemical Equation Present) Practical catalyst: A magnetic nanoparticle-supported palladium catalyst was developed for the highly efficient heterogeneous Suzuki, Sonogashira, and Stille couplings of a wide variety of aryl chlorides. Furthermore, the catalyst could be recycled by facile magnetic separation without any loss of activity. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA,.
引用
收藏
页码:1119 / 1122
页数:4
相关论文
共 50 条
  • [31] A simple and efficient protocol for Suzuki coupling reactions of aryl chlorides and aryl bromides in aqueous DMF
    Liu, Leifang
    Wang, Wendi
    Xiao, Chuanyong
    JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2014, 749 : 83 - 87
  • [32] Sila-Sonogashira Cross-Coupling Reactions of Activated Aryl Chlorides with Alkynylsilanes
    Nishihara, Yasushi
    Inoue, Eiji
    Okada, Yoshiaki
    Takagi, Kentaro
    SYNLETT, 2008, (19) : 3041 - 3045
  • [33] Diaminophosphine oxides as preligands for Ni-catalyzed Suzuki cross-coupling reactions of aryl chlorides with arylboronic acids
    Hu, Feng
    Kumpati, Blessy N.
    Lei, Xiangyang
    TETRAHEDRON LETTERS, 2014, 55 (52) : 7215 - 7218
  • [34] Application of Biaryl Phosphacycles in Palladium-Catalysed Suzuki-Miyaura Cross-Coupling Reactions of Aryl Chlorides
    Lamola, Jairus L.
    Moshapo, Paseka T.
    Holzapfel, Cedric W.
    Maumela, Munaka Christopher
    EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2024, 27 (17)
  • [35] A highly active catalyst for the room-temperature amination and Suzuki coupling of aryl chlorides
    Wolfe, JP
    Buchwald, SL
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1999, 38 (16) : 2413 - 2416
  • [36] In situ generated 1-alkylbenzimidazole-palladium catalyst for the Suzuki coupling of aryl chlorides
    Özdemir, I
    Sahin, N
    Gök, Y
    Demir, S
    Çetinkaya, B
    JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2005, 234 (1-2) : 181 - 185
  • [37] Pd/C: An Efficient, Heterogeneous and Reusable Catalyst for Phosphane-Free Carbonylative Suzuki Coupling Reactions of Aryl and Heteroaryl Iodides
    Khedkar, Mayur V.
    Tambade, Pawan J.
    Qureshi, Ziyauddin S.
    Bhanage, Bhalchandra M.
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2010, 2010 (36) : 6981 - 6986
  • [38] Suzuki-Miyaura coupling reactions of aryl chlorides catalyzed by a new nickel(II) σ-aryl complex
    Lei, Xiangyang
    Obregon, Karla A.
    Alla, Jhansi
    APPLIED ORGANOMETALLIC CHEMISTRY, 2013, 27 (07) : 419 - 424
  • [39] A convenient high activity catalyst for the Sonogashira coupling of aryl bromides
    Köllhofer, A
    Plenio, H
    ADVANCED SYNTHESIS & CATALYSIS, 2005, 347 (09) : 1295 - 1300
  • [40] Palladium-Catalyzed Suzuki-Miyaura Coupling Reactions of Boronic Acid Derivatives with Aryl Chlorides
    Zhou, Zihong
    Zhang, Yaqi
    Xia, Wang
    Chen, Huixuan
    Liang, Hao
    He, Xuefeng
    Yu, Sifan
    Cao, Rihui
    Qiu, Liqin
    ASIAN JOURNAL OF ORGANIC CHEMISTRY, 2016, 5 (10) : 1260 - 1268