Issue 29, 2011

Visible light-induced intramolecular cyclization reactions of diamines: a new strategy to construct tetrahydroimidazoles

Abstract

A new and efficient synthesis of highly substituted tetrahydroimidazole derivatives by means of visible light-induced intramolecular cyclization reactions has been described. This photoredox catalytic reaction exhibited high diastereoselectivity and afforded the desired products in good yields.

Graphical abstract: Visible light-induced intramolecular cyclization reactions of diamines: a new strategy to construct tetrahydroimidazoles

Supplementary files

Article information

Article type
Communication
Submitted
17 Apr 2011
Accepted
09 Jun 2011
First published
23 Jun 2011

Chem. Commun., 2011,47, 8337-8339

Visible light-induced intramolecular cyclization reactions of diamines: a new strategy to construct tetrahydroimidazoles

J. Xuan, Y. Cheng, J. An, L. Lu, X. Zhang and W. Xiao, Chem. Commun., 2011, 47, 8337 DOI: 10.1039/C1CC12203G

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