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RETRACTED: The amine-catalysed Suzuki-Miyaura-type coupling of aryl halides and arylboronic acids (Retracted Article)
被引:17
|作者:
Xu, Lei
[1
]
Liu, Fu-Yue
[1
]
Zhang, Qi
[1
]
Chang, Wei-Jun
[1
]
Liu, Zhong-Lin
[1
]
Lv, Ying
[2
]
Yu, Hai-Zhu
[2
]
Xu, Jun
[1
]
Dai, Jian-Jun
[1
]
Xu, Hua-Jian
[1
]
机构:
[1] Hefei Univ Technol, Anhui Prov Key Lab Adv Catalyt Mat & React Engn, Inst Ind & Equipment Technol, Sch Food & Biol Engn,Sch Chem & Chem Engn, Hefei, Peoples R China
[2] Anhui Univ, Dept Chem, Anhui Prov Key Lab Chem Inorgan Organ Hybrid Func, Hefei, Peoples R China
基金:
中国国家自然科学基金;
关键词:
PINCER COMPLEXES;
METAL;
PALLADIUM;
DERIVATIVES;
MECHANISMS;
EFFICIENT;
RECEPTOR;
BIARYLS;
ALKYNES;
D O I:
10.1038/s41929-020-00564-z
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Suzuki-Miyaura coupling is a practical and attractive carbon-carbon bond formation reaction due to its high efficiency and wide functional group compatibility, but its industrial applications are limited because it is typically catalysed by expensive palladium-containing transition-metal complexes. Here we show a robust and chemoselective organocatalytic Suzuki-Miyaura-type coupling of aryl halides with arylboronic acids catalysed by amines. The utility and scope of this reaction were demonstrated by the synthesis of several commercially relevant small molecules and a selection of derivatives of pharmaceutical drugs.
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页码:71 / 78
页数:8
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