化学
分子内力
环加成
区域选择性
分子间力
蒽醌类
蒽醌
取代基
光化学
氢键
芳基
分子
药物化学
有机化学
催化作用
烷基
生物
植物
作者
Fanyuanhang Yang,Ping Lin,Biping Xu,Yuzhen Gao,Weiping Su
出处
期刊:Organic Letters
[American Chemical Society]
日期:2023-11-13
卷期号:25 (46): 8308-8313
被引量:1
标识
DOI:10.1021/acs.orglett.3c03354
摘要
The formation of intramolecular hydrogen bonds in anthraquinones makes them inert to photoinduced reactions; therefore, it is a great challenge to phototransform these compounds. Herein, we reported a formal visible-light-induced [4 + 2] cycloaddition of both 1-hydroxyanthraquinones and 1-aminoanthraquinones with olefins under external photocatalyst-free conditions with high regioselectivity. More than 60 substrates are disclosed, demonstrating the reliability of this protocol to construct diverse functionalized anthraquinone derivatives.
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