Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
49922 | Catalysis Communications | 2015 | 4 Pages |
Abstract
•Excellent green catalytic system for the nickel-catalysed Suzuki reaction•Efficient yield for aryl halides with arylboronic acids in ionic liquids•Large amount of synthesis using a simple and economical process
An efficient strategy for the nickel-catalysed synthesis of biaryls and terphenyls has been developed in environmentally-friendly reaction media. In the presence of β-diketone and PPh3 ligands, Ni(TFA)2 acted as an effective catalyst for the Suzuki–Miyaura cross-coupling of aryl halides and arylboronic acids in an ionic liquid solution. Biaryls and terphenyls were obtained in good yields under this catalytic system.
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Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Man Wang, Xiaobin Yuan, Hongyu Li, Limin Ren, Zhizhong Sun, Yanjun Hou, Wenyi Chu,