Supported Palladium-Catalyzed Carbonylative Synthesis of Diaryl Ketones from Aryl Bromides and Arylboronic Acids

被引：14
|
作者：
Xu, Tiefeng [1 ]
Wang, Qi [2 ]
Yang, Zeyi [1 ]
Yi, Lili [1 ]
Wang, Jian-Shu [2 ]
Lu, Wangyang [1 ]
Ying, Jun [2 ]
Wu, Xiao-Feng [3 ,4 ]
机构：
[1] Zhejiang Sci Tech Univ, Natl Engn Lab Text Fiber Mat & Proc Technol, Hangzhou 310018, Peoples R China
[2] Zhejiang Sci Tech Univ, Dept Chem, Key Lab Surface & Interface Sci Polymer Mat Zheji, Hangzhou 310018, Peoples R China
[3] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Liaoning, Peoples R China
[4] Univ Rostock, Leibniz Inst Katalyse eV, Albert Einstein Str 29a, D-18059 Rostock, Germany
来源：
CHEMISTRY-AN ASIAN JOURNAL | 2021年 / 16卷 / 15期
基金：
浙江省自然科学基金;
关键词：
Palladium catalysis; Carbonylation; Suzuki coupling; Ketone; Heterogeneous catalyst; FRIEDEL-CRAFTS ACYLATION; IONIC LIQUIDS; AGENTS;
D O I：
10.1002/asia.202100540
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
A palladium supported on graphitic carbon nitride (Pd/g-C3N4) catalyzed carbonylative reaction of aryl bromides and arylboronic acids by has been developed for the construction of diaryl ketones. Using benzene-1,3,5-triyl triformate (TFBen) as the CO source, the reaction proceeded well to give various diaryl ketones in moderate to good yields.
引用
收藏
页码：2027 / 2030
页数：4
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