Mechanism and Selectivity in Nickel-Catalyzed Cross-Electrophile Coupling of Aryl Halides with Alkyl Halides

被引:533
作者
Biswas, Soumik [1 ]
Weix, Daniel J. [1 ]
机构
[1] Univ Rochester, Dept Chem, Rochester, NY 14627 USA
关键词
FUNCTIONALIZED GRIGNARD-REAGENTS; REDUCTIVE CONJUGATE ADDITION; CARBON BOND FORMATION; OXIDATIVE ADDITION; RADICAL CATALYSIS; ORGANIC HALIDES; AROMATIC HALIDES; KETONE FORMATION; DIRECT ARYLATION; COMPLEXES;
D O I
10.1021/ja407589e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The direct cross-coupling of two different electrophiles, such as an aryl halide with an alkyl halide, offers many advantages over conventional cross-coupling methods that require a carbon nucleophile. Despite its promise as a versatile synthetic strategy, a limited understanding of the mechanism and origin of cross selectivity has hindered progress in reaction development and design. Herein, we shed light on the mechanism for the nickel-catalyzed cross-electrophile coupling of aryl halides with alkyl halides and demonstrate that the selectivity arises from an unusual catalytic cycle that combines both polar and radical steps to form the new C-C bond.
引用
收藏
页码:16192 / 16197
页数:6
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共 80 条
[1]   Transition-Metal-Catalyzed Direct Arylation of (Hetero)Arenes by C-H Bond Cleavage [J].
Ackermann, Lutz ;
Vicente, Ruben ;
Kapdi, Anant R. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (52) :9792-9826
[2]   Aryl-aryl bond formation by transition-metal-catalyzed direct arylation [J].
Alberico, Dino ;
Scott, Mark E. ;
Lautens, Mark .
CHEMICAL REVIEWS, 2007, 107 (01) :174-238
[3]   Homoleptic Organoderivatives of High-Valent Nickel(III) [J].
Alonso, Pablo J. ;
Arauzo, Ana B. ;
Angeles Garcia-Monforte, Maria ;
Martin, Antonio ;
Menjon, Babil ;
Rillo, Conrado ;
Tomas, Milagros .
CHEMISTRY-A EUROPEAN JOURNAL, 2009, 15 (41) :11020-11030
[4]   RATES AND MECHANISM OF BIPHENYL SYNTHESIS CATALYZED BY ELECTROGENERATED COORDINATIVELY UNSATURATED NICKEL-COMPLEXES [J].
AMATORE, C ;
JUTAND, A .
ORGANOMETALLICS, 1988, 7 (10) :2203-2214
[5]   Synthesis of functionalised diarylmethanes via a cobalt-catalysed cross-coupling of arylzinc species with benzyl chlorides [J].
Amatore, Muriel ;
Gosmini, Corinne .
CHEMICAL COMMUNICATIONS, 2008, (40) :5019-5021
[6]   Direct Method for Carbon-Carbon Bond Formation: The Functional Group Tolerant Cobalt-Catalyzed Alkylation of Aryl Halides [J].
Amatore, Muriel ;
Gosmini, Corinne .
CHEMISTRY-A EUROPEAN JOURNAL, 2010, 16 (20) :5848-5852
[7]   Evidence for a NiI active species in the catalytic cross-coupling of alkyl electrophiles [J].
Anderson, TJ ;
Jones, GD ;
Vicic, DA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (26) :8100-8101
[8]   COMPETING NUCLEOPHILIC DISPLACEMENT AND RADICAL CHAIN REDUCTION IN REACTIONS OF TRANSITION-METAL HYDRIDE ANIONS WITH ALKYL BROMIDES [J].
ASH, CE ;
HURD, PW ;
DARENSBOURG, MY ;
NEWCOMB, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1987, 109 (11) :3313-3317
[9]   OXIDATIVE ADDITION TO IRIDIUM(I) .1. FREE-RADICAL PROCESS [J].
BRADLEY, JS ;
CONNOR, DE ;
DOLPHIN, D ;
OSBORN, JA ;
LABINGER, JA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (11) :4043-&
[10]   Bimetallic Oxidative Addition Involving Radical Intermediates in Nickel-Catalyzed Alkyl-Alkyl Kumada Coupling Reactions [J].
Breitenfeld, Jan ;
Ruiz, Jesus ;
Wodrich, Matthew D. ;
Hu, Xile .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (32) :12004-12012