Issue 19, 2023

Ir(iii)-catalyzed decarbonylative annulation of salicylaldehydes with cyclohexane-1,3-diones

Abstract

An efficient Ir(III)-catalyzed decarbonylative annulation of salicylaldehydes with cyclohexane-1,3-diones has been achieved via the in situ generated iodonium ylides. The reaction proceeds smoothly under mild and operationally simple conditions, affording a variety of benzofuran derivatives in moderate to high yields with good functional group tolerance. Moreover, the large-scale synthesis and further modification of the products highlight the utility of this protocol.

Graphical abstract: Ir(iii)-catalyzed decarbonylative annulation of salicylaldehydes with cyclohexane-1,3-diones

Supplementary files

Article information

Article type
Paper
Submitted
27 Oct 2022
Accepted
03 Apr 2023
First published
26 Apr 2023

New J. Chem., 2023,47, 9421-9426

Ir(III)-catalyzed decarbonylative annulation of salicylaldehydes with cyclohexane-1,3-diones

Q. Jiang, Y. Min, Y. Liu, H. Li, J. Peng and C. Liu, New J. Chem., 2023, 47, 9421 DOI: 10.1039/D2NJ05242C

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