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A General Palladium-Catalyzed Amination of Aryl Halides with Ammonia
被引:150
|作者:
Schulz, Thomas
[1
]
Torborg, Christian
[1
]
Enthaler, Stephan
[1
]
Schaeffner, Benjamin
[1
]
Dumrath, Andreas
[1
]
Spannenberg, Anke
[1
]
Neumann, Helfried
[1
]
Boerner, Armin
[1
]
Beller, Matthias
[1
]
机构:
[1] Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
关键词:
amination;
anilines;
homogeneous catalysis;
palladium;
phosphanes;
CROSS-COUPLING REACTIONS;
HIGHLY EFFICIENT CATALYST;
BOND-FORMING REACTIONS;
LONG-LIVED CATALYSTS;
C-N;
PRIMARY AMINES;
REDUCTIVE CARBONYLATION;
HETEROARYL BROMIDES;
OXIDATIVE ADDITION;
CARBENE CATALYSTS;
D O I:
10.1002/chem.200802678
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
A study was conducted to demonstrate palladium(Pd)-catalyzed amination of aryl halides with ammonia. The active catalyst was formed in situ from Pd(OAc)2, along with air- and moisture stable phosphines as pre-catalysts. It was found that the productivity of the catalyst system was similar to that of competitive Pd and phosphine systems. It was demonstrated that the novel electron-rich sterically demanding phosphine ligand was unable to be displaced from the palladium by ammonia to a significant extent, which prevented the deactivation of the catalyst by the ligand. It was also demonstrated that the Pd-catalyzed animation worked at ambient pressure. It was observed that the optimized system showed an excellent substrate scope including deactivated, electron-neutral, and activated halides, o-, m- p-substituted substrates, aryl chlorides, and heterocycles.
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页码:4528 / 4533
页数:6
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