Photoredox-catalysed arylamination of non-anomeric exoglycals with aryl sulfinamides via radical Smiles rearrangement

Abstract

Non-anomeric exocyclic glycals have received less research attention while 1,2-glycals are widely studied as synthetic precursors for oligosaccharides and glycosylation. This study addresses this gap by utilizing photoredox conditions while aryl sulfinamides as bifunctional reagents to modify non-anomeric exocyclic glycals, thereby synthesizing a series of 5-aryl-6-amino glycosyl derivatives under mild conditions.

Supplementary files

Article information

Article type
Communication
Submitted
28 Jan 2026
Accepted
25 Feb 2026
First published
27 Feb 2026

Chem. Commun., 2026, Accepted Manuscript

Photoredox-catalysed arylamination of non-anomeric exoglycals with aryl sulfinamides via radical Smiles rearrangement

Y. Jiao, C. Li, R. Wang and S. Yu, Chem. Commun., 2026, Accepted Manuscript , DOI: 10.1039/D6CC00579A

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