Issue 6, 2018

Visible-light-induced iminyl radical formation via electron-donor–acceptor complexes: a photocatalyst-free approach to phenanthridines and quinolines

Abstract

A visible light-induced synthesis of nitrogen-containing arenes from O-2,4-dinitrophenyl oximes has been reported. This photochemical strategy is photocatalyst-free and enabled by electron-donor–acceptor (EDA) complexes of O-2,4-dinitrophenyl oximes and Et3N. A variety of highly functionalized nitrogen-containing arenes, including 15 phenanthridines and 8 quinolines, were synthesized in excellent yields.

Graphical abstract: Visible-light-induced iminyl radical formation via electron-donor–acceptor complexes: a photocatalyst-free approach to phenanthridines and quinolines

Supplementary files

Article information

Article type
Research Article
Submitted
31 Oct 2017
Accepted
22 Dec 2017
First published
22 Dec 2017

Org. Chem. Front., 2018,5, 977-981

Visible-light-induced iminyl radical formation via electron-donor–acceptor complexes: a photocatalyst-free approach to phenanthridines and quinolines

J. Sun, Y. He, X. An, X. Zhang, L. Yu and S. Yu, Org. Chem. Front., 2018, 5, 977 DOI: 10.1039/C7QO00992E

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