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Development of Palladium Precatalysts that Efficiently Generate LPd(0) Active Species
被引:64
作者:
Shaughnessy, Kevin H.
[1
]
机构:
[1] Univ Alabama, Dept Chem & Biochem, Tuscaloosa, AL 35487 USA
基金:
美国国家科学基金会;
关键词:
palladium;
cross-coupling;
carbene ligands;
phosphine ligands;
precatalysts;
N-HETEROCYCLIC CARBENE;
CROSS-COUPLING REACTIONS;
BUCHWALD-HARTWIG AMINATION;
SUZUKI-MIYAURA REACTION;
DINUCLEAR PD(I) COMPLEXES;
PD-PEPPSI COMPLEXES;
ROOM-TEMPERATURE;
C-N;
CATALYZED AMINATION;
ARYL CHLORIDES;
D O I:
10.1002/ijch.201900067
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Palladium catalysts have become central to modern organic synthesis, particularly in the context of cross-coupling reactions to form C-C and C-heteroatom bonds. The development of highly efficient catalyst systems has seen a transition from the use of in situ-generated catalysts derived from a ligand source and palladium precursor to the use of preformed palladium-ligand complexes that can efficiently generate the active species. The design of these systems has focused on optimizing the generation of the LPd(0) species presumed to be the active catalysts with most state-of-the-art ligand systems. This review will highlight the development of Pd(0), Pd(I), and Pd(II) precatalysts that efficiently generate LPd(0) active species with a focus on their activation mechanisms and applications in catalysis.
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页码:180 / 194
页数:15
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