Borate-mediated aryl polyfluoroalkoxylation under transition-metal-free conditions

被引:3
|
作者
Kikushima, Kotaro [1 ]
Tsuda, Tomoka [1 ]
Miyamoto, Naoki [1 ]
Kita, Yasuyuki [2 ]
Dohi, Toshifumi [1 ,2 ]
机构
[1] Ritsumeikan Univ, Coll Pharmaceut Sci, Kusatsu, Shiga 5258577, Japan
[2] Ritsumeikan Univ, Res Org Sci & Technol, Kusatsu, Shiga 5258577, Japan
关键词
SUBSTITUTION; CHLORIDES; ETHERS;
D O I
10.1039/d4cc04008b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We describe the transition-metal-free coupling for polyfluoroalkoxy arenes using polyfluoroalkoxy borates, which serve as counterions to diaryliodonium salts and transferring mediators of polyfluoroalkoxy groups. This strategy demonstrates high functional group compatibility owing to the low nucleophilicity of the borate mediator, thus offering a practical approach for synthesizing diverse polyfluoroalkoxy arenes. We report boron-intermediary ligand transfer of diaryliodonium salt, synthesizing polyfluorolalkyl aryl ethers in the absence of transition metal catalyst or base.
引用
收藏
页码:10552 / 10555
页数:4
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