Issue 27, 2019

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

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.

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

Supplementary files

Article information

Article type
Communication
Submitted
27 May 2019
Accepted
21 Jun 2019
First published
21 Jun 2019

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

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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