A user-friendly, all-purpose Pd-NHC (NHC=N-heterocyclic carbene) precatalyst for the Negishi reaction: A step towards a universal cross-coupling catalyst

被引:395
作者
Organ, Michael G. [1 ]
Avola, Stephanie [1 ]
Dubovyk, Igor [1 ]
Hadei, Niloufar [1 ]
Kantchev, Eric Assen B. [1 ]
O'Brien, Christopher J. [1 ]
Valente, Cory [1 ]
机构
[1] York Univ, Dept Chem, N York, ON M3J 1P3, Canada
关键词
alkanes; biaryls; C-C coupling; heterocycles; palladium;
D O I
10.1002/chem.200600206
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have developed the first user-friendly Negishi protocol capable of routinely cross-coupling all combinations of alkyl and aryl centers. The use of an easily synthesized, air stable, highly active, well-defined precatalyst PEPPSI-IPr (1; PEPPSI=pyridine-enhanced precatalyst preparation, stabilization and initiation; IPr=diisopropylphenylimidazolium derivative) substantially increases the scope, reliability, and ease-of-use of the Negishi reaction. All organolialides and routinely used pseudohalides were excellent coupling partners, with the use of chlorides, bromides, iodides, triflates, tosylates, and mesylates resulting in high yield of the coupled product. Furthermore, all reactions were performed by using general laboratory techniques, with no glove-box necessary as the precatalyst was weighed and stored in air. Utilization of this methodology allowed for the easy synthesis of an assortment of sterically encumbered biaryls and druglike heteroaromatics, demonstrating the value of the PEPPSI-IPr system. Furthermore, this is also the first time Pd-NHC (NHC=N-heterocyclic carbene) methodology has surpassed the related phosphine-ligated Negishi processes both in activity and use.
引用
收藏
页码:4749 / 4755
页数:7
相关论文
共 59 条
[1]   Palladium complexes of 1,3,5,7-tetramethyl-2,4,8-trioxa-6-phenyl-6-phosphaadamantane:: Synthesis, crystal structure and use in the Suzuki and Sonogashira reactions and the α-arylation of ketones [J].
Adjabeng, G ;
Brenstrum, T ;
Frampton, CS ;
Robertson, AJ ;
Hillhouse, J ;
McNulty, J ;
Capretta, A .
JOURNAL OF ORGANIC CHEMISTRY, 2004, 69 (15) :5082-5086
[2]  
[Anonymous], ANGEW CHEM
[3]   Catalysts for Suzuki-Miyaura coupling processes: Scope and studies of the effect of ligand structure [J].
Barder, TE ;
Walker, SD ;
Martinelli, JR ;
Buchwald, SL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (13) :4685-4696
[4]   Phosphaadamantanes as ligands for palladium catalyzed cross-coupling chemistry:: Library synthesis, characterization, and screening in the Suzuki coupling of alkyl halides and tosylates containing β-hydrogens with boronic acids and alkylboranes [J].
Brenstrum, T ;
Gerristma, DA ;
Adjabeng, GM ;
Frampton, CS ;
Britten, J ;
Robertson, AJ ;
McNulty, J ;
Capretta, A .
JOURNAL OF ORGANIC CHEMISTRY, 2004, 69 (22) :7635-7639
[5]   Co-ordination chemistry of 6-(2-hydroxyphenyl)pyridine-2-carboxylic acid: a terdentate ligand with a mixed phenolate/pyridyl/carboxylate donor set [J].
Couchman, SM ;
Jeffery, JC ;
Thornton, P ;
Ward, MD .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1998, (07) :1163-1169
[6]  
De Meijere A., 2004, Metal-Catalyzed Cross-Coupling Reactions
[7]   Synthesis and characterization of N-heterocyclic carbene phospha-palladacycles and their properties in Heck catalysis [J].
Frey, GD ;
Schütz, J ;
Herdtweck, E ;
Herrmann, WA .
ORGANOMETALLICS, 2005, 24 (18) :4416-4426
[8]  
Frisch A., 2005, ANGEW CHEM, V117, P680
[9]   First Kumada reaction of alkyl chlorides using N-heterocyclic carbene/palladium catalyst systems [J].
Frisch, AC ;
Rataboul, F ;
Zapf, A ;
Beller, M .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2003, 687 (02) :403-409
[10]   Suzuki-Miyaura cross-coupling reactions mediated by palladium/imidazolium salt systems [J].
Grasa, GA ;
Viciu, MS ;
Huang, JK ;
Zhang, CM ;
Trudell, ML ;
Nolan, SP .
ORGANOMETALLICS, 2002, 21 (14) :2866-2873