Issue 20, 2021

Photoredox halogenation of quinolones: the dual role of halo-fluorescein dyes

Abstract

An efficient C-3 halogenation of quinolin-4-ones is reported with halogenated fluorescein dyes which serve both as a halogen source and photocatalyst. This reaction shows broad substrate scope and gives good to excellent yields of C-3 brominated/iodinated quinolones with eosin Y/rose bengal in green light under ambient conditions. The mechanistic investigations suggest a radical pathway involving the oxidative dehalogenation of the dye in the presence of air.

Graphical abstract: Photoredox halogenation of quinolones: the dual role of halo-fluorescein dyes

Supplementary files

Article information

Article type
Paper
Submitted
19 Mar 2021
Accepted
20 Apr 2021
First published
20 Apr 2021

Org. Biomol. Chem., 2021,19, 4585-4592

Photoredox halogenation of quinolones: the dual role of halo-fluorescein dyes

Ritu, S. Kumar, P. Chauhan and N. Jain, Org. Biomol. Chem., 2021, 19, 4585 DOI: 10.1039/D1OB00538C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements