Bisphosphines: A Prominent Ancillary Ligand Class for Application in Nickel-Catalyzed C-N Cross-Coupling

被引:119
作者
Lavoie, Christopher M. [1 ]
Stradiotto, Mark [1 ]
机构
[1] Dalhousie Univ, Dept Chem, 6274 Coburg Rd,POB 15000, Halifax, NS B3H 4R2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
nickel; C-N cross-coupling; ligand design; bisphophines; anilines; BUCHWALD-HARTWIG AMINATION; ARYL CHLORIDES; BOND FORMATION; (HETERO)ARYL CHLORIDES; AROMATIC AMINATIONS; PRIMARY ALKYLAMINES; OXIDATIVE ADDITION; EFFICIENT CATALYST; TRANSITION-METAL; KEY ROLES;
D O I
10.1021/acscatal.8b01879
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The Ni-catalyzed Csp2N cross-coupling of NH substrates and (hetero)aryl (pseudo)halides for the synthesis of (hetero)anilines is in the midst of a resurgence. Reactivity breakthroughs that have been achieved in this field within the past five years have served to establish Ni catalysis as being competitive with, and in some cases superior to, more well-established Pd- or Cu-based protocols. Whereas the repurposing of useful ancillary ligands from the Pd domain has been the most frequently employed approach in the quest to develop effective Ni-based catalysts for such transformations, considerable progress has been made as of late in the design of ancillary ligands tailored specifically for use with Ni. Bisphosphine ancillary ligands have proven to be well-suited for such an approach, given their modular and facile syntheses; several variants have emerged recently that are particularly effective in enabling a range of otherwise challenging Ni-catalyzed Csp2N cross-couplings. This Perspective presents a comprehensive summary of the advancements within the field of Ni-catalyzed Csp2N cross-coupling through the application of the bisphosphine ancillary ligand class. It is our intention that the discussion of key ancillary ligand design concepts and mechanistic considerations presented herein will provide a useful platform for researchers to initiate ancillary ligand design efforts for the development of high-performing Ni cross-coupling catalysts.
引用
收藏
页码:7228 / 7250
页数:45
相关论文
共 137 条
[81]   Rapid room temperature Buchwald-Hartwig and Suzuki-Miyaura couplings of heteroaromatic compounds employing low catalyst loadings [J].
Navarro, Oscar ;
Marion, Nicolas ;
Mei, Jianguo ;
Nolan, Steven P. .
CHEMISTRY-A EUROPEAN JOURNAL, 2006, 12 (19) :5142-5148
[82]   Nickel(II) complex incorporating methylene bridged tetradentate dicarbene ligand as an efficient catalyst toward C-C and C-N bond formation reactions [J].
Nirmala, Muthukumaran ;
Prakash, Govindan ;
Ramachandran, Rangasamy ;
Viswanathamurthi, Periasamy ;
Malecki, Jan Grzegorz ;
Linert, Wolfgang .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2015, 397 :56-67
[83]   Efficient nickel-mediated intramolecular amination of aryl chlorides [J].
Omar-Amrani, R ;
Thomas, A ;
Brenner, E ;
Schneider, R ;
Fort, Y .
ORGANIC LETTERS, 2003, 5 (13) :2311-2314
[84]   Non-covalent interactions and thermochemistry using XDM-corrected hybrid and range-separated hybrid density functionals [J].
Otero-de-la-Roza, A. ;
Johnson, Erin R. .
JOURNAL OF CHEMICAL PHYSICS, 2013, 138 (20)
[85]   A triazine-phosphite polymeric ligand bearing cage-like P, N-ligation sites: an efficient ligand in the nickel-catalyzed amination of aryl chlorides and phenols [J].
Panahi, Farhad ;
Roozbin, Fatemeh ;
Rahimi, Sajjad ;
Moayyed, Mohammadesmaeil ;
Valaei, Aria ;
Iranpoor, Nasser .
RSC ADVANCES, 2016, 6 (84) :80670-80678
[86]   Development of an Air-Stable Nickel Precatalyst for the Amination of Aryl Chlorides, Sulfamates, Mesylates, and Triflates [J].
Park, Nathaniel H. ;
Teverovskiy, Georgiy ;
Buchwald, Stephen L. .
ORGANIC LETTERS, 2014, 16 (01) :220-223
[87]  
Pringle P. G., 2012, PHOSPHORUS 3 LIGANDS, P391, DOI DOI 10.1002/9781118299715.CH13
[88]   Nickel-Catalyzed Amination of Aryl Sulfamates [J].
Ramgren, Stephen D. ;
Silberstein, Amanda L. ;
Yang, Yang ;
Garg, Neil K. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (09) :2171-2173
[89]   Nickel N-Heterocyclic Carbene-Catalyzed C-Heteroatom Bond Formation, Reduction, and Oxidation: Reactions and Mechanistic Aspects [J].
Ritleng, Vincent ;
Henrion, Mickael ;
Chetcuti, Michael J. .
ACS CATALYSIS, 2016, 6 (02) :890-906
[90]   The Medicinal Chemist's Toolbox: An Analysis of Reactions Used in the Pursuit of Drug Candidates [J].
Roughley, Stephen D. ;
Jordan, Allan M. .
JOURNAL OF MEDICINAL CHEMISTRY, 2011, 54 (10) :3451-3479