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

Ya Peng; Cheng-Tao Feng; Yu-Qing Li; Feng-Xiang Chen; Kun Xu

doi:10.1039/C9OB01227C

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

Ya Peng,^a Cheng-Tao Feng,

*^a Yu-Qing Li,^a Feng-Xiang Chen^a and Kun Xu

*^b

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* Corresponding authors

^a School of Chemical Engineering, Anhui University of Science and Technology, Huainan, Anhui, China
E-mail: fengct2010@163.com

^b Engineering Technology Research Center of Henan Province for Photo- and Electrochemical Catalysis, School of Chemistry and Pharmaceutical Engineering, Nanyang Normal University, Nanyang, Henan, China

Abstract

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.

This article is part of the themed collection: Synthetic methodology in OBC

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Article information

DOI: https://doi.org/10.1039/C9OB01227C
Article type: Communication
Submitted: 27 May 2019
Accepted: 21 Jun 2019
First published: 21 Jun 2019

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Org. Biomol. Chem., 2019,17, 6570-6573

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

Y. Peng, C. Feng, Y. Li, F. Chen and K. Xu, Org. Biomol. Chem., 2019, 17, 6570 DOI: 10.1039/C9OB01227C

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Organic & Biomolecular Chemistry

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

Abstract

Supplementary files

Article information

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

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