Metal- and photocatalyst-free approach to visible-light-induced acylation of quinoxalinones

Abstract

A transition-metal- and photocatalyst-free photochemical reaction was successfully developed for the direct acylation of quinoxalin-2(1H)-ones, which was enabled by the formation of electron donor–acceptor (EDA) complexes. The use of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) as the electron donor allows efficient and operationally simple access to a series of C3-aroylated and acylated quinoxalin-2(1H)-ones with moderate to good yields.

Graphical abstract: Metal- and photocatalyst-free approach to visible-light-induced acylation of quinoxalinones

Supplementary files

Article information

Article type
Paper
Submitted
17 Apr 2024
Accepted
29 Apr 2024
First published
30 Apr 2024

Org. Biomol. Chem., 2024, Advance Article

Metal- and photocatalyst-free approach to visible-light-induced acylation of quinoxalinones

W. Niwetmarin, N. Saesian, R. Saruengkhanphasit, C. Eurtivong, N. Thasana and S. Ruchirawat, Org. Biomol. Chem., 2024, Advance Article , DOI: 10.1039/D4OB00630E

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