Visible-Light-Promoted [3+2] Cycloaddition of 2H-Azirines with Quinones: Access to Substituted Benzo[f]isoindole-4,9-diones

被引：15

作者：

Wang, Lijia ^{[1
]}

Liu, Chuang ^{[1
]}

Li, Lei ^{[1
]}

Wang, Xin ^{[1
]}

Sun, Ran ^{[1
]}

Zhou, Ming-Dong ^{[1
]}

Wang, He ^{[1
]}

机构：

[1] Liaoning Petrochem Univ, Sch Petrochem Engn, Fushun 113001, Liaoning, Peoples R China

来源：

CHINESE JOURNAL OF CHEMISTRY | 2022年 / 40卷 / 06期

基金：

中国国家自然科学基金;

关键词：

Photocatalysis; Cycloaddition; Quinones; 2H-Azirines; Benzo[f]isoindole-4; 9-diones; 1,3-DIPOLAR CYCLOADDITION; AROMATIZATION SEQUENCE; PHOTOREDOX CATALYSIS; CHEMISTRY; PYRIDINES; 3-PHENYL-2H-AZIRINES; CYCLIZATION; PYRAZINES; CLEAVAGE;

D O I：

10.1002/cjoc.202100728

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Comprehensive Summary A visible-light-promoteded [3 + 2] cycloaddition reaction of 2H-azirines with quinones has been developed under mild reaction conditions. The reaction provides a general and efficient strategy for the synthesis of the benzo[f]isoindole-4,9-diones scaffold via a tandem [3 + 2] cyclization/oxidative aromatization with molecular oxygen. Furthermore, preliminary studies for photocatalytic properties show that the benzo[f]isoindole-4,9-diones 3 can be used as photocatalysts in several organic transformations.

引用

页码：719 / 724

页数：6

共 37 条

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