Nickel-catalyzed electrochemical Minisci acylation of aromatic N-heterocycles with α-keto acids via ligand-to-metal electron transfer pathway

被引:46
作者
Ding, Hang [1 ]
Xu, Kun [1 ]
Zeng, Cheng-Chu [1 ]
机构
[1] Beijing Univ Technol, Coll Life Sci & Bioengn, Beijing Key Lab Environm & Viral Oncol, Beijing 100124, Peoples R China
基金
中国国家自然科学基金;
关键词
Minisci acylation reactions; Nickel-catalysis; alpha-Keto acid; Electrosynthesis; DECARBOXYLATIVE ACYLATION; REDOX CATALYSTS; HETEROARENES; CYCLIZATION; RADICALS; NITROGEN;
D O I
10.1016/j.jcat.2019.10.030
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 nickel-catalyzed electrochemical methodology for the Minisci acylation of aromatic electron-deficient heterocycles with alpha-keto acids has been developed. The reaction is performed in an undivided cell under constant current conditions, featuring broad scope of substrates and avoiding the conventional utilization of silver-based catalysts in conjunction with excess amount of oxidants. Cyclic voltammetric analysis disclosed that a ligand-to-metal electron transfer process may be involved in the generation of the key acyl radicals. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:38 / 43
页数:6
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