Graphitic Carbon Nitride as a Photocatalyst for Decarboxylative C(sp2)-C(sp3) Couplings via Nickel Catalysis

被引:7
|
作者
Lukas, Florian [1 ]
Findlay, Michael T. [1 ]
Fillols, Meritxell [1 ]
Templ, Johanna [1 ,2 ]
Savino, Elia [1 ]
Martin, Benjamin [3 ]
Allmendinger, Simon [3 ]
Furegati, Markus [3 ]
Noel, Timothy [1 ]
机构
[1] Univ Amsterdam, Vant Hoff Inst Mol Sci HIMS, Flow Chem Grp, Sci Pk 904, NL-1098 XH Amsterdam, Netherlands
[2] TU Wien, Inst Appl Synthet Chem, Getreidemarkt 9-E163, A-1060 Vienna, Austria
[3] Novartis Pharm AG, Fabrikstr, CH-4002 Basel, Switzerland
基金
欧洲研究理事会;
关键词
Graphitic Carbon Nitride; Decarboxylation; Heterogeneous Photocatalyst; Metallaphotoredox; Nickel; CARBOXYLIC-ACIDS; ARYL HALIDES; AMINO-ACIDS; PHOTOREDOX; ARYLATION; STRATEGY; ENABLES;
D O I
10.1002/anie.202405902
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of robust and reliable methods for the construction of C(sp(2))-C(sp(3)) bonds is vital for accessing an increased array of structurally diverse scaffolds in drug discovery and development campaigns. While significant advances towards this goal have been achieved using metallaphotoredox chemistry, many of these methods utilise photocatalysts based on precious-metals due to their efficient redox processes and tuneable properties. However, due to the cost, scarcity, and toxicity of these metals, the search for suitable replacements should be a priority. Here, we show the use of commercially available heterogeneous semiconductor graphitic carbon nitride (gCN) as a photocatalyst, combined with nickel catalysis, for the cross-coupling between aryl halide and carboxylic acid coupling partners. gCN has been shown to engage in single-electron-transfer (SET) and energy-transfer (EnT) processes for the formation of C-X bonds, and in this manuscript we overcome previous limitations to furnish C-C over C-O bonds using carboxylic acids. A broad scope of both aryl halides and carboxylic acids is presented, and recycling of the photocatalyst demonstrated. The mechanism of the reaction is also investigated.
引用
收藏
页数:9
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