Exploring the ring-opening reactions of imidazo[1,5-a]quinolines for the synthesis of imides under photochemical conditions

被引：14
|
作者：
Peng, Ya [1 ]
Feng, Cheng-Tao [1 ]
Li, Yu-Qing [1 ]
Chen, Feng-Xiang [1 ]
Xu, Kun [2 ]
机构：
[1] Anhui Univ Sci & Technol, Sch Chem Engn, Huainan 232001, Anhui, Peoples R China
[2] Nanyang Normal Univ, Engn Technol Res Ctr Henan Prov Photo & Electroch, Sch Chem & Pharmaceut Engn, Nanyang 473061, Henan, Peoples R China
来源：
ORGANIC & BIOMOLECULAR CHEMISTRY | 2019年 / 17卷 / 27期
基金：
中国国家自然科学基金;
关键词：
PHOTOREDOX CATALYSIS; SINGLET OXYGEN; OXIDATION; ALDEHYDES; ACIDS; ALKYL;
D O I：
10.1039/c9ob01227c
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The ring-opening reaction of imidazo[1,5-a]quinolines under photoredox conditions has been described. With Eosin Y as the organophotoredox catalyst, synthetically useful and medicinally important imides were obtained in moderate to excellent yields under mild reaction conditions.
引用
收藏
页码：6570 / 6573
页数：4
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