Visible-light-induced diastereoselective synthesis of β-lactams via a Cu(i)-catalyzed cascade 1,5-H shift/cyclization

Abstract

We herein report a visible-light-driven, copper(I)-catalyzed intramolecular 1,5-hydrogen atom transfer (1,5 HAT)/cyclization that provides efficient access to β-lactams with good to excellent diastereoselectivity. The copper catalyst plays a dual role, functioning both as a photosensitizer and as a Lewis acid to facilitate the cyclization step. Notably, the diastereoselectivity of the terminal cyclization can be effectively modulated through ligand design, marking a key advance in energy transfer catalysis. This work represents a notable advance in copper photocatalysis and offers an efficient, environmentally benign route to β-lactam scaffolds.

Graphical abstract: Visible-light-induced diastereoselective synthesis of β-lactams via a Cu(i)-catalyzed cascade 1,5-H shift/cyclization

Supplementary files

Article information

Article type
Research Article
Submitted
06 Mar 2026
Accepted
21 Apr 2026
First published
29 Apr 2026

Org. Chem. Front., 2026, Advance Article

Visible-light-induced diastereoselective synthesis of β-lactams via a Cu(I)-catalyzed cascade 1,5-H shift/cyclization

K. Zhang, S. Li, H. Zhou, F. Zhang, L. Guo, Y. Li and Z. Jiao, Org. Chem. Front., 2026, Advance Article , DOI: 10.1039/D6QO00281A

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