Aromatic trifluoromethyldenitration and trifluoromethyldecyanation using trifluoromethyltrimethylsilane
被引:12
作者:
Adams, DJ
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机构:
Univ York, Dept Chem, York YO1 5DD, N Yorkshire, EnglandUniv York, Dept Chem, York YO1 5DD, N Yorkshire, England
Adams, DJ
[1
]
Clark, JH
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机构:
Univ York, Dept Chem, York YO1 5DD, N Yorkshire, EnglandUniv York, Dept Chem, York YO1 5DD, N Yorkshire, England
Clark, JH
[1
]
Hansen, LB
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机构:
Univ York, Dept Chem, York YO1 5DD, N Yorkshire, EnglandUniv York, Dept Chem, York YO1 5DD, N Yorkshire, England
Hansen, LB
[1
]
Sanders, VC
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机构:
Univ York, Dept Chem, York YO1 5DD, N Yorkshire, EnglandUniv York, Dept Chem, York YO1 5DD, N Yorkshire, England
Sanders, VC
[1
]
Tavener, SJ
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h-index: 0
机构:
Univ York, Dept Chem, York YO1 5DD, N Yorkshire, EnglandUniv York, Dept Chem, York YO1 5DD, N Yorkshire, England
Tavener, SJ
[1
]
机构:
[1] Univ York, Dept Chem, York YO1 5DD, N Yorkshire, England
来源:
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
|
1998年
/
18期
关键词:
D O I:
10.1039/a805079a
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Activation of trifluoromethyltrimethylsilane by potassium fluoride in N,N-dimethylacetamide provides a powerful source of trifluoromethide which is capable of substituting aromatic nitro and cyano groups under nucleophilic conditions, albeit in low yield. The trifluoromethide generated in this system is also a potent base which leads to a number of interesting side reactions via deprotonation of the substrate.