Issue 46, 2025

ortho-C–O arylation of aromatic amides with Grignard reagents through the Meyers reaction

Abstract

ortho-C–O arylation of arylamides is a step-efficient and straightforward approach for the construction of biphenyl amides, yet achieving it in practice remains a great challenge. Herein, we address this challenge by developing an efficient ortho-C–O arylation of various aryl amides with Grignard reagents through a Meyers-type reaction mechanism, performed in the absence of transition-metal catalysts. This protocol enables the selective synthesis of diverse biphenyl amides, featuring high yields and broad substrate scope.

Graphical abstract: ortho-C–O arylation of aromatic amides with Grignard reagents through the Meyers reaction

Supplementary files

Transparent peer review

To support increased transparency, we offer authors the option to publish the peer review history alongside their article.

View this article’s peer review history

Article information

Article type
Communication
Submitted
03 Sep 2025
Accepted
29 Oct 2025
First published
30 Oct 2025

Org. Biomol. Chem., 2025,23, 10469-10473

ortho-C–O arylation of aromatic amides with Grignard reagents through the Meyers reaction

Y. Wu, B. Wang, Y. Shi, P. Liu and J. Kong, Org. Biomol. Chem., 2025, 23, 10469 DOI: 10.1039/D5OB01418B

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