Metal-Free C-H Borylation of N-Heteroarenes by Boron Trifluoride

被引:19
|
作者
Iashin, Vladimir [1 ]
Berta, Denes [2 ]
Chernichenko, Konstantin [1 ,3 ]
Nieger, Martin [1 ]
Moslova, Karina [1 ]
Papai, Imre [2 ]
Repo, Timo [1 ]
机构
[1] Univ Helsinki, Dept Chem, AI Virtasen Aukio 1, Helsinki 00014, Finland
[2] Res Ctr Nat Sci, Inst Organ Chem, Magyar Tudosok Korutja 2, H-1117 Budapest, Hungary
[3] Janssen Pharmaceut NV, API Small Mol Dev, Turnhoutseweg 30, B-2340 Beerse, Belgium
基金
芬兰科学院;
关键词
boron trifluoride; borylation; C-H activation; frustrated Lewis pairs; protodeboronation; FRUSTRATED-LEWIS-PAIR; BOND ACTIVATION; REACTIVITY; ARENE; GENERATION; COMPLEXES; MECHANISM; SALTS;
D O I
10.1002/chem.202001436
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Organoboron compounds are essential reagents in modern C-C coupling reactions. Their synthesis via catalytic C-H borylation by main group elements is emerging as a powerful tool alternative to transition metal based catalysis. Herein, a straightforward metal-free synthesis of aryldifluoroboranes from BF(3)and heteroarenes is reported. The reaction is assisted by sterically hindered amines and catalytic amounts of thioureas. According to computational studies the reaction proceeds via frustrated Lewis pair (FLP) mechanism. The obtained aryldifluoroboranes are further stabilized against destructive protodeborylation by converting them to the corresponding air stable tetramethylammonium organotrifluoroborates.
引用
收藏
页码:13873 / 13879
页数:7
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