Intermolecular amination of ethyl benzo ylacetate via photocatalytic nitrene transfer reactions

Abstract

In this study, we report on a C–H functionalization of 1,3-dicarbonyl compounds via a photocatalytic nitrene transfer reaction. A wide range of 1,3-dicarbonyl substrates and iodinanes were found compatible with the reaction conditions to directly afford the C–H functionalization products without the need of preformation of nucleophilic enolate equivalents. Additionally, a comprehensive series of synthetic applications and control experiments were conducted, thereby further extending the practical utility of this approach.

Graphical abstract: Intermolecular amination of ethyl benzo ylacetate via photocatalytic nitrene transfer reactions

Supplementary files

Article information

Article type
Research Article
Submitted
26 Nov 2024
Accepted
06 Jan 2025
First published
08 Jan 2025

Org. Chem. Front., 2025, Advance Article

Intermolecular amination of ethyl benzo ylacetate via photocatalytic nitrene transfer reactions

Y. Guo, Y. Guo, L. Ding, L. Shi, X. Hao and R. M. Koenigs, Org. Chem. Front., 2025, Advance Article , DOI: 10.1039/D4QO02194K

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