Access to Electron-Rich Dibenzofurans through NBu4OAc-Mediated Palladium Catalysis

被引:1
|
作者
Power, Mark [1 ,2 ]
Mackey, Katrina [1 ,2 ]
Light, Mark E. [3 ]
Jones, David J. [4 ]
Mcglacken, Gerard P. [1 ,2 ]
机构
[1] Univ Coll Cork Ireland, Sch Chem, Cork T12YN60, Ireland
[2] Univ Coll Cork, Analyt & Biol Chem Res Facil ABCRF, Cork T12YN60, Ireland
[3] Univ Southampton, Chem Dept, Univ Rd, Southampton SO17 1BJ, England
[4] Univ Edinburgh, EaStCHEM Sch Chem, Joseph Black Bldg,David Brewster Rd, Edinburgh EH9 3FJ, Scotland
基金
爱尔兰科学基金会;
关键词
Dibenzofuran; palladium; catalysis; tetraalkylammonium salt; electron-rich; INTRAMOLECULAR DIRECT ARYLATION; C-H ACTIVATION; BROMIDES; IODIDES; ACIDS;
D O I
10.1002/ejoc.202300790
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Dibenzofuran and its derivatives are ubiquitous and important medicinal and natural products. Many contain electron-rich aryl rings. Forming the key intramolecular Ar-Ar bond using traditional cross-coupling is difficult. The C-H functionalisation (C-H activation) approach is, in principle, far more useful. However, we previously found that the well-established conditions, which promote C-H functionalisation through Concerted Metalation-Deprotonation (CMD), proved unsatisfactory. Herein, we report a Pd-catalysed C-H functionalisation protocol that works with electron-rich arenes. We use tetrabutylammonium acetate (NBu4OAc), which we suspect can act as base, ligand and solvent, rendering this protocol a simple and efficient route to electron-rich dibenzofurans.
引用
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页数:5
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