Intramolecular photoredox reactions of 1,2-naphthoquinone derivatives

被引：9
|
作者：
Ando, Yoshio [1 ]
Wakita, Fumihiro [1 ]
Ohmori, Ken [1 ]
Suzuki, Keisuke [1 ]
机构：
[1] Tokyo Inst Technol, Dept Chem, Meguro Ku, 2-12-1 O Okayama, Tokyo 1528551, Japan
来源：
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS | 2018年 / 28卷 / 16期
关键词：
Photoreaction; Redox reaction; 1,2-Naphthoquinone; C-H functionalization;
D O I：
10.1016/j.bmcl.2018.05.056
中图分类号：
R914 [药物化学];
学科分类号：
100701 ;
摘要：
Photoirraditation of substituted 1,2-naphthoquinones gives the corresponding oxacycle via intramolecular redox reaction, which enabled net C-H functionalization of the proximal position to the excited carbonyl group of the quinones. The substrate scope and mechanistic insights are described.
引用
收藏
页码：2663 / 2666
页数：4
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