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Nickel-catalyzed carboxylation of aryl iodides with lithium formate through catalytic CO recycling
被引:16
作者:
Wu, Ya-Nan
[1
]
Fu, Ming-Chen
[1
]
Shang, Rui
[1
,2
]
Fu, Yao
[1
]
机构:
[1] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, CAS Key Lab Urban Pollutant Convers, Anhui Prov Key Lab Biomass Clean Energy,iChEM, Hefei 230026, Peoples R China
[2] Univ Tokyo, Sch Sci, Dept Chem, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1130033, Japan
基金:
中国国家自然科学基金;
中国博士后科学基金;
国家重点研发计划;
关键词:
FORMIC-ACID;
HYDROCARBOXYLATION;
HALIDES;
ALKYNES;
CARBONYLATION;
PD;
HYDROXYCARBONYLATION;
HYDROFORMYLATION;
OLEFINS;
D O I:
10.1039/d0cc01363c
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
A protocol for the Ni-catalyzed carboxylation of aryl iodides with formate has been developed with good functional group compatibility for the synthesis of a variety of aromatic carboxylic acids under mild conditions. The reaction tolerates other functionalities for cross-coupling, such as aryl bromide, aryl chloride, aryl tosylate, and aryl pinacol boronate. The reaction proceeds through a carbonylation process with in situ generated carbon monoxide in the presence of a catalytic amount of acetic anhydride and lithium formate, avoiding the use of gaseous CO. The strategy of CO recycling in catalytic amounts is critical for the success of the reaction.
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页码:4067 / 4069
页数:3
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