Well-defined nickel and palladium precatalysts for cross-coupling

被引:376
作者
Hazari, Nilay [1 ]
Melvin, Patrick R. [1 ]
Beromi, Megan Mohadjer [1 ]
机构
[1] Yale Univ, Dept Chem, POB 208107, New Haven, CT 06520 USA
基金
美国国家科学基金会;
关键词
SUZUKI-MIYAURA REACTION; PD-CATALYZED FLUORINATION; DINUCLEAR PD(I) COMPLEXES; ROOM-TEMPERATURE; C-N; GRIGNARD-REAGENTS; ALKYL-HALIDES; SUPPORTED PRECATALYSTS; HETEROCYCLIC CARBENE; ARYL MESYLATES;
D O I
10.1038/s41570-017-0025
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition metal-catalysed cross-coupling is one of the most powerful synthetic methods and has led to vast improvements in the synthesis of pharmaceuticals, agrochemicals and precursors for materials chemistry. A major advance in cross-coupling over the past 20 years is the utilization of well-defined, bench-stable Pd and Ni precatalysts that do not require the addition of free ancillary ligand, which can hinder catalysis by occupying open coordination sites on the metal. The development of precatalysts has resulted in new reactions and expanded substrate scopes, enabling transformations under milder conditions and with lower catalyst loadings. This Review highlights recent advances in the development of Pd and Ni precatalysts for cross-coupling, and provides a critical comparison between the state of the art in Pd- and Ni-based systems.
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页数:16
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共 176 条
  • [1] Decarbonylative C-H Coupling of Azoles and Aryl Esters: Unprecedented Nickel Catalysis and Application to the Synthesis of Muscoride A
    Amaike, Kazuma
    Muto, Kei
    Yamaguchi, Junichiro
    Itami, Kenichiro
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (33) : 13573 - 13576
  • [2] Mechanism of the nickel-catalyzed electrosynthesis of ketones by heterocoupling of aryl and benzyl halides
    Amatore, C
    Jutand, A
    Périchon, J
    Rollin, Y
    [J]. MONATSHEFTE FUR CHEMIE, 2000, 131 (12): : 1293 - 1304
  • [3] Nickel: The "Spirited Horse" of Transition Metal Catalysis
    Ananikov, Valentine P.
    [J]. ACS CATALYSIS, 2015, 5 (03): : 1964 - 1971
  • [4] Evidence for a NiI active species in the catalytic cross-coupling of alkyl electrophiles
    Anderson, TJ
    Jones, GD
    Vicic, DA
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (26) : 8100 - 8101
  • [5] Nickel-Catalyzed Cross-Electrophile Coupling with Organic Reductants in Non-Amide Solvents
    Anka-Lufford, Lukiana L.
    Huihui, Kierra M. M.
    Gower, Nicholas J.
    Ackerman, Laura K. G.
    Weix, Daniel J.
    [J]. CHEMISTRY-A EUROPEAN JOURNAL, 2016, 22 (33) : 11564 - 11567
  • [6] [Anonymous], 2004, ANGEW CHEM
  • [7] N,N-Diethyl O-Carbamate: Directed Metalation Group and Orthogonal Suzuki-Miyaura Cross-Coupling Partner
    Antoft-Finch, Aurora
    Blackburn, Tom
    Snieckus, Victor
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (49) : 17750 - 17752
  • [8] Dialkyl Ether Formation by Nickel-Catalyzed Cross-Coupling of Acetals and Aryl Iodides
    Arendt, Kevin M.
    Doyle, Abigail G.
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2015, 54 (34) : 9876 - 9880
  • [9] Pd-PEPPSI-IHeptCl: A General-Purpose, Highly Reactive Catalyst for the Selective Coupling of Secondary Alkyl Organozincs
    Atwater, Bruce
    Chandrasoma, Nalin
    Mitchell, David
    Rodriguez, Michael J.
    Organ, Michael G.
    [J]. CHEMISTRY-A EUROPEAN JOURNAL, 2016, 22 (41) : 14531 - 14534
  • [10] The Selective Cross-Coupling of Secondary Alkyl Zinc Reagents to Five-Membered-Ring Heterocycles Using Pd-PEPPSI-IHeptCl
    Atwater, Bruce
    Chandrasoma, Nalin
    Mitchell, David
    Rodriguez, Michael J.
    Pompeo, Matthew
    Froese, Robert D. J.
    Organ, Michael G.
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2015, 54 (33) : 9502 - +