Issue 14, 2022

Electrochemical formal [3 + 2] cycloaddition of azobenzenes with hexahydro-1,3,5-triazines

Abstract

A catalyst-free electrochemical [3 + 2] cycloaddition of azobenzenes with hexahydro-1,3,5-triazines in the absence of any external oxidant is developed for constructing the 1,2,4-triazolidine skeleton; here 35 examples are displayed. The unique electrochemical cycloaddition features wide substrate scope, excellent functional group tolerance and satisfactory yields. Mechanistic experiments support the reaction pathway proposed for the [3 + 2] cycloaddition.

Graphical abstract: Electrochemical formal [3 + 2] cycloaddition of azobenzenes with hexahydro-1,3,5-triazines

Supplementary files

Article information

Article type
Research Article
Submitted
31 Mar 2022
Accepted
06 Jun 2022
First published
06 Jun 2022

Org. Chem. Front., 2022,9, 3769-3774

Electrochemical formal [3 + 2] cycloaddition of azobenzenes with hexahydro-1,3,5-triazines

C. Li, Q. Zhong, S. Tang, L. Wang, P. Li and H. Li, Org. Chem. Front., 2022, 9, 3769 DOI: 10.1039/D2QO00530A

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