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Copper(II)-Catalyzed C-N Coupling of Aryl Halides and N-Nucleophiles Promoted by Quebrachitol or Diethylene Glycol
被引:8
|作者:
Du, Fangyu
[1
]
Zhou, Qifan
[1
]
Fu, Yang
[1
]
Chen, Yuanguang
[1
]
Wu, Ying
[2
]
Chen, Guoliang
[1
]
机构:
[1] Shenyang Pharmaceut Univ, Key Lab Struct Based Drug Design & Discovery, Minist Educ, Shenyang 110016, Liaoning, Peoples R China
[2] Yunnan Inst Trop Crops, Jinghong 666100, Peoples R China
来源:
关键词:
N-arylation;
quebrachitol;
diethylene glycol;
Cu(OAc)(2);
Ullman coupling;
AROMATIC-SUBSTITUTION;
(HETERO)ARYL HALIDES;
COPPER;
LIGANDS;
TAMIBAROTENE;
AMIDATION;
AMINATION;
TACRINE;
ANALOGS;
D O I:
10.1055/s-0039-1690707
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Herein, we report the natural ligand quebrachitol (QCT) as a promoter for a Cu(II) catalyst, which is highly effective for N-arylation of various amines and related aryl halides. A series of diarylamine derivatives were obtained in high yields by using diethylene glycol (DEG) as both ligand and solvent. The C-N coupling reactions proceed under mild conditions and exhibit good functional group tolerance.
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页码:2161 / 2168
页数:8
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