详细信息
An Efficient Palladium and Bis(2-pyridylmethyl)amine-based System for Suzuki-Miyaura Cross-Coupling under Aqueous and Aerobic Condition ( SCI-EXPANDED收录)
文献类型:期刊文献
中文题名:An Efficient Palladium and Bis(2-pyridylmethyl)amine-based System for Suzuki-Miyaura Cross-Coupling under Aqueous and Aerobic Condition
英文题名:An Efficient Palladium and Bis(2-pyridylmethyl)amine-based System for Suzuki-Miyaura Cross-Coupling under Aqueous and Aerobic Condition
作者:Yu Jianjun;Wang Limin[1];Liu Mingtao;Qiu Jun;Shen Qiang;Fang Lei;Tang Jun
机构:[1]E China Univ Sci & Technol, Shanghai Key Lab Funct Mat Chem, Shanghai 200237, Peoples R China; E China Univ Sci & Technol, Inst Fine Chem, Shanghai 200237, Peoples R China
年份:2012
卷号:30
期号:5
起止页码:1114
中文期刊名:Chinese Journal of Chemistry
外文期刊名:CHINESE JOURNAL OF CHEMISTRY
收录:;Scopus;WOS:【SCI-EXPANDED(收录号:WOS:000304045600018),CCR-EXPANDED(收录号:WOS:000304045600018)】;CSCD:【CSCD2011_2012】;
基金:This work was financially supported by the National Natural Science Foundation of China (No. 20672035).
语种:英文
中文关键词:Suzuki-Miyaura cross-coupling;bis(2-pyridylmethyl)amine-based ligand;arylboronic acids;aryl halides
外文关键词:Suzuki-Miyaura cross-coupling; bis(2-pyridylmethyl)amine-based ligand; arylboronic acids; aryl halides
摘要:A novel PdC12/bis(2-pyridylmethyl)amine-based ligand (1) catalytic system, which is water-soluble and air-stable, has been successfully synthesized and applied for Suzuki-Miyaura cross-coupling reaction. In the presence of catalytic amount of PdCl2/1 system, arylboronic acids can couple with a wide range of aryl halides, including aryl bromides and aryl chlorides. The reactions proceed under mild conditions to give excellent yields, and a wide range of functionalities is tolerated.
A novel PdCl2/bis(2-pyridylmethyl)amine-based ligand (1) catalytic system, which is water-soluble and air-stable, has been successfully synthesized and applied for Suzuki-Miyaura cross-coupling reaction. In the presence of catalytic amount of PdCl2/1 system, arylboronic acids can couple with a wide range of aryl halides, including aryl bromides and aryl chlorides. The reactions proceed under mild conditions to give excellent yields, and a wide range of functionalities is tolerated.
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