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An efficient palladium-NHC (NHC=N-heterocyclic carbene) and aryl amination pre-catalyst : [Pd(IPr*)(cinnamyl)Cl]

(2012) ADVANCED SYNTHESIS & CATALYSIS. 354(10). p.1897-1901
Author
Organization
Abstract
The well-defined [Pd(IPr*)(cinnamyl)Cl] complex is reported as one of the best N-heterocyclic carbene (NHC)-based pre-catalysts for the BuchwaldHartwig amination reaction. This catalytic system displays high efficiency for the coupling of numerous (hetero)aryl chlorides, with a wide range of amines, at room temperature or at extremely low catalyst loading (as low as 0.025 mol%).
Keywords
amination, Buchwald-Hartwig cross-coupling, N-heterocyclic carbene, palladium, CROSS-COUPLING REACTIONS, TEMPERATURE SUZUKI-MIYAURA, LONG-LIVED CATALYSTS, BUCHWALD-HARTWIG, BOND FORMATION, (NHC)PD(ALLYL)CL NHC, C-N, CHLORIDES, COMPLEXES, BROMIDES

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Chicago
Chartoire, Anthony, Xavier Frogneux, and Steven Nolan. 2012. “An Efficient palladium-NHC (NHC=N-heterocyclic Carbene) and Aryl Amination Pre-catalyst : [Pd(IPr*)(cinnamyl)Cl].” Advanced Synthesis & Catalysis 354 (10): 1897–1901.
APA
Chartoire, A., Frogneux, X., & Nolan, S. (2012). An efficient palladium-NHC (NHC=N-heterocyclic carbene) and aryl amination pre-catalyst : [Pd(IPr*)(cinnamyl)Cl]. ADVANCED SYNTHESIS & CATALYSIS, 354(10), 1897–1901.
Vancouver
1.
Chartoire A, Frogneux X, Nolan S. An efficient palladium-NHC (NHC=N-heterocyclic carbene) and aryl amination pre-catalyst : [Pd(IPr*)(cinnamyl)Cl]. ADVANCED SYNTHESIS & CATALYSIS. 2012;354(10):1897–901.
MLA
Chartoire, Anthony, Xavier Frogneux, and Steven Nolan. “An Efficient palladium-NHC (NHC=N-heterocyclic Carbene) and Aryl Amination Pre-catalyst : [Pd(IPr*)(cinnamyl)Cl].” ADVANCED SYNTHESIS & CATALYSIS 354.10 (2012): 1897–1901. Print.
@article{8168883,
  abstract     = {The well-defined [Pd(IPr*)(cinnamyl)Cl] complex is reported as one of the best N-heterocyclic carbene (NHC)-based pre-catalysts for the BuchwaldHartwig amination reaction. This catalytic system displays high efficiency for the coupling of numerous (hetero)aryl chlorides, with a wide range of amines, at room temperature or at extremely low catalyst loading (as low as 0.025 mol%).},
  author       = {Chartoire, Anthony and Frogneux, Xavier and Nolan, Steven},
  issn         = {1615-4150},
  journal      = {ADVANCED SYNTHESIS & CATALYSIS},
  keywords     = {amination,Buchwald-Hartwig cross-coupling,N-heterocyclic carbene,palladium,CROSS-COUPLING REACTIONS,TEMPERATURE SUZUKI-MIYAURA,LONG-LIVED CATALYSTS,BUCHWALD-HARTWIG,BOND FORMATION,(NHC)PD(ALLYL)CL NHC,C-N,CHLORIDES,COMPLEXES,BROMIDES},
  language     = {eng},
  number       = {10},
  pages        = {1897--1901},
  title        = {An efficient palladium-NHC (NHC=N-heterocyclic carbene) and aryl amination pre-catalyst : [Pd(IPr*)(cinnamyl)Cl]},
  url          = {http://dx.doi.org/10.1002/adsc.201200207},
  volume       = {354},
  year         = {2012},
}

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