Metal-free Synthesis of α‑keto‑N‑acyl sulfoximines from Sulfoximine and α-Bromomethyl aryl ketones under Photoredox catalysis

Abstract

In this study, we describe a metal-free and mild strategy to prepare α‑keto‑N‑acyl sulfoximines through the reactions of sulfoximines with phenacyl bromide under green LED in the presence of eosin-Y as a photocatalyst. This protocol operates without the need for external oxidants and enables the formation of new C–O and C–N bonds. This method offers a sustainable and efficient approach for constructing valuable sulfoximine-based organic frameworks.

Supplementary files

Article information

Article type
Communication
Submitted
17 Oct 2025
Accepted
11 Dec 2025
First published
15 Dec 2025

Org. Biomol. Chem., 2025, Accepted Manuscript

Metal-free Synthesis of α‑keto‑N‑acyl sulfoximines from Sulfoximine and α-Bromomethyl aryl ketones under Photoredox catalysis

V. Navaneetha Krishnan, K. Natarajan, P. P. R. Vetrivel, A. H. A. Mercy and G. C. Nandi, Org. Biomol. Chem., 2025, Accepted Manuscript , DOI: 10.1039/D5OB01642H

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