Room-Temperature C-H Bond Functionalization by Merging Cobalt and Photoredox Catalysis

被引:108
|
作者
Kalsi, Deepti [1 ]
Dutta, Subhradeep [1 ]
Barsu, Nagaraju [1 ]
Rueping, Magnus [2 ]
Sundararaju, Basker [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Fine Chem Lab, Kanpur 208016, Uttar Pradesh, India
[2] Rhein Westfal TH Aachen, Inst Organ Chem, Landoltweg 1, D-52074 Aachen, Germany
来源
ACS CATALYSIS | 2018年 / 8卷 / 09期
关键词
C-H bond functionalization; cobalt; photocatalysis; room temperature; amide; annulation; VISIBLE-LIGHT PHOTOREDOX; NICKEL CATALYSIS; CARBON-HYDROGEN; HECK REACTIONS; ACTIVATION; ARYLATION; ALKYNES; PALLADIUM; GOLD; CARBONYLATION;
D O I
10.1021/acscatal.8b02118
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A non-noble metal-free protocol has been developed for C-H bond functionalization at room temperature by merging cobalt-mediated catalysis with photo-catalysis. The reaction requires only oxygen as sole oxidant and operated at room temperature under redox-neutral conditions. Visible-light activated photoredox catalyst functions as an electron transfer reagent with oxygen as a terminal oxidant in the cobalt-mediated C-H and N-H bond annulation. The developed methodology allows annulations with various coupling partners. The concept demonstrated herein is expected to enhance the scope of cobalt catalysis as applied to sustainable fine chemical synthesis.
引用
收藏
页码:8115 / 8120
页数:11
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