Organophotocatalytic pyridination of N-arylglycines with 4-cyanopyridines by decarboxylative and decyanative radical-radical coupling

被引:1
|
作者
Pan, Changduo [1 ]
Xiang, Chengli [2 ]
Yu, Jin-Tao [2 ]
机构
[1] Jiangsu Univ Technol, Sch Chem & Chem Engn, Changzhou 213001, Peoples R China
[2] Changzhou Univ, Sch Petrochem Engn, Changzhou 213164, Peoples R China
关键词
ALPHA-AMINO-ACIDS; DERIVATIVES; ARYLATION; CYANOPYRIDINES; SUBSTITUTION; CATALYSIS; ALKENES;
D O I
10.1039/d4ob01257g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A photocatalytic decarboxylative aminoalkylation of 4-cyanopyridines with N-arylglycines is achieved, providing 4-(aminomethyl)pyridine derivatives in moderate to good yields. This organic photocatalytic reaction undergoes a radical-radical cross-coupling process under redox-neutral conditions, featuring simple operation, readily available N-arylglycines and a broad substrate scope. Mechanistic investigations indicated that a proton-coupled electron-transfer process was involved to enable the single electron transfer between the reduced photocatalyst and 4-cyanopyridine in the presence of N-arylglycines.
引用
收藏
页码:7806 / 7810
页数:5
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