Issue 16, 2024

Photo-induced synthesis of fluoroalkylated quinolinones via an iron-catalyzed LMCT decarboxylation process

Abstract

Herein, we report a practical synthetic method for the efficient preparation of fluoroalkylated quinoline-2,4-diones using N-(2-cyanophenyl)-N-methylacrylamides as substrates, fluoroalkyl carboxylic acids as reactants, and Fe(OH)(OAc)2 as a catalyst. This reaction started with a photo-driven ligand-to-metal charge transfer (LMCT) process to decarboxylate the reactant and produce fluoroalkyl radicals, which then underwent radical cascade cyclization with the substrate. The target products were obtained in 55–91% yields. A gram scale experiment was also completed using a continuous-flow photocatalytic device.

Graphical abstract: Photo-induced synthesis of fluoroalkylated quinolinones via an iron-catalyzed LMCT decarboxylation process

Supplementary files

Article information

Article type
Research Article
Submitted
18 Apr 2024
Accepted
15 Jun 2024
First published
18 Jun 2024

Org. Chem. Front., 2024,11, 4436-4441

Photo-induced synthesis of fluoroalkylated quinolinones via an iron-catalyzed LMCT decarboxylation process

Z. Song, L. Guo, C. Yang and W. Xia, Org. Chem. Front., 2024, 11, 4436 DOI: 10.1039/D4QO00707G

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