Visible light-induced metal-free chemoselective oxidative cleavage of benzyl C-heteroatom (N, S, Se) bonds utilizing organoboron photocatalysts

被引:9
作者
Wei, Lanfeng [1 ,3 ]
Bai, Wenbo [2 ]
Hu, Zhiyan [2 ]
Yang, Zhiyong [1 ,3 ]
Xu, Liang [2 ]
机构
[1] Xinjiang Inst Engn, Sch Safety Sci & Engn, Urumqi 830000, Peoples R China
[2] Shihezi Univ, Sch Chem & Chem Engn, State Key Lab Incubat Base Green Proc Chem Engn, Shihezi 832003, Peoples R China
[3] Xinjiang Inst Engn, Minist Educ, Key Lab Coal Resources & Green Min Xinjiang, Urumqi 830023, Peoples R China
关键词
HETEROGENEOUS PHOTOCATALYST; CARBONYL-COMPOUNDS; FREE CATALYST; ALCOHOLS; AMINES;
D O I
10.1039/d3cc04073a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The oxidation process is widely explored and used to synthesize diverse organic chemicals. Herein, a unified metal-free photooxidative platform for the cleavage of C-heteroatom bonds has been developed. In these reactions, the aminoquinolate diarylboron (AQDAB) complex is utilized as the photocatalyst, instigating the oxidation process induced by visible light. The cleavage of C-heteroatom bonds can be achieved chemoselectively, affording the formal carbonylation product of C-N, C-S, and C-Se bonds. This method provides a channel for connecting amines, thiols, or selenides with the carbonyl compounds directly, broadening the potential applications of oxidation as a synthetic tool. We have established a photooxidation system, which can realize formal carbonylation of C-heteroatom (N, S, Se) bonds.
引用
收藏
页码:13344 / 13347
页数:4
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