Direct C-N coupling of azoles with ethers via oxidative C-H activation under metal-organic framework catalysis

被引:20
作者
Nguyen, Khoa D. [1 ]
Doan, Son H. [1 ]
Ngo, Anh N. V. [1 ]
Nguyen, Tung T. [1 ]
Phan, Nam T. S. [1 ]
机构
[1] HCMC Univ Technol, Dept Chem Engn, VNU HCM, 268 Ly Thuong Kiet,Dist 10, Ho Chi Minh City, Vietnam
关键词
Azoles; Coupling; C-H activation; Fe3O(BPDC)(3); Ethers; HETEROGENEOUS CATALYSTS; BOND ADJACENT; IRON; EFFICIENT; FUNCTIONALIZATION; WATER; THIOETHERS; ALKYLATION; ARYLATION; NITROGEN;
D O I
10.1016/j.jiec.2016.08.025
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A metal-organic framework Fe3O(BPDC)(3) was synthesized, and used as a productive heterogeneous catalyst for the direct C-N coupling of azoles with ethers via oxidative C-H activation to produce azole derivatives. The MOF-based catalyst displayed higher catalytic efficiency than many homogeneous catalysts as well as several MOFs in the transformation. The MOF-based catalyst could be reused many times for the synthesis of azole derivatives by the direct C-N coupling of azoles with ethers without a noteworthy deterioration in catalytic efficiency. To the best of our knowledge, this direct C-N coupling reaction was not previously performed in the presence of heterogeneous catalysts. (C) 2016 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:136 / 145
页数:10
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