Photoinduced FeCl₃-Catalyzed α-C(sp³)-H Azolation of Primary Aliphatic Alcohols via LMCT-Driven HAT

Abstract

Herein, a visible-light-driven FeCl₃-catalyzed α-C(sp³)-H azolation/coupling reaction of primary aliphatic alcohols has been reported. The reaction achieves activation of the α-C(sp 3 )-H bond in the ether formed by dehydration of primary alcohols under mild conditions via an LMCT-promoted HAT process. The protocol is broadly applicable to substituted indazoles and other nitrogen-containing scaffolds common in medicinal chemistry, and is compatible with a wide range of primary aliphatic alcohols substrates. HAT O Scheme 1 α-C(sp 3 )-H azolation of ether or alcohols

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
Paper
Submitted
04 Feb 2026
Accepted
30 Mar 2026
First published
31 Mar 2026

Org. Biomol. Chem., 2025, Accepted Manuscript

Photoinduced FeCl₃-Catalyzed α-C(sp³)-H Azolation of Primary Aliphatic Alcohols via LMCT-Driven HAT

W. Zeng, S. Zhan, R. Huang, M. Yuan, J. Zhang and Y. Jin, Org. Biomol. Chem., 2025, Accepted Manuscript , DOI: 10.1039/D6OB00200E

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