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Electrochemical decarboxylative alkylation of ß-ketoacids with phenol derivatives.
Wang, Shan; Wu, Zhaotian; Li, Junqiang; Zhu, Yujun; Zheng, Shaojun; Jiang, Chunhui; Lu, Hongfei.
Afiliación
  • Wang S; School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang, Jiangsu 212100, China. chemjiang@just.edu.cn.
  • Wu Z; School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang, Jiangsu 212100, China. chemjiang@just.edu.cn.
  • Li J; School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang, Jiangsu 212100, China. chemjiang@just.edu.cn.
  • Zhu Y; School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang, Jiangsu 212100, China. chemjiang@just.edu.cn.
  • Zheng S; School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang, Jiangsu 212100, China. chemjiang@just.edu.cn.
  • Jiang C; School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang, Jiangsu 212100, China. chemjiang@just.edu.cn.
  • Lu H; School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang, Jiangsu 212100, China. chemjiang@just.edu.cn.
Chem Commun (Camb) ; 60(10): 1329-1332, 2024 Jan 30.
Article en En | MEDLINE | ID: mdl-38197300
ABSTRACT
An electrochemical method for the decarboxylative alkylation of ß-ketoacids with phenol derivatives has been developed. The protocol was carried out in readily available unseparated cells at room temperature in the absence of catalysts and oxidants. The corresponding aryl ketones were obtained in satisfactory yields without additional electrolytes, and were easy to produce in gram-scale synthesis. Based on control experiments and cyclic voltammetry, a plausible reaction mechanism was proposed.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: China