Issue 17, 2025

Mn-catalyzed oxo-alkylation of 1,2,4-triazine-3,5(2H,4H)-diones with cyclic alkanols via oxidative cross-dehydrogenative coupling

Abstract

An efficient and convenient pathway to synthesize diverse 3 or 4-oxo-alkyl substituted 1,2,4-triazine-3,5(2H,4H)-diones has been reported via an atom- and step-economical cross-dehydrogenation coupling strategy with good functional group tolerance and wide substrate scope. The present transformation employs inexpensive manganese salt catalysts and iodobenzene diacetate oxidants at room temperature. The synthetic utility of this pathway is further demonstrated by a gram scale reaction.

Graphical abstract: Mn-catalyzed oxo-alkylation of 1,2,4-triazine-3,5(2H,4H)-diones with cyclic alkanols via oxidative cross-dehydrogenative coupling

Supplementary files

Article information

Article type
Paper
Submitted
20 Jan 2025
Accepted
24 Mar 2025
First published
27 Mar 2025

Org. Biomol. Chem., 2025,23, 4161-4165

Mn-catalyzed oxo-alkylation of 1,2,4-triazine-3,5(2H,4H)-diones with cyclic alkanols via oxidative cross-dehydrogenative coupling

Q. Liang, S. Bai, Y. Tan, H. Zhang, Y. Zhang and J. Zhao, Org. Biomol. Chem., 2025, 23, 4161 DOI: 10.1039/D5OB00098J

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