Photocatalytic regioselective four-component radical relay carbonylation for α-aminoketones synthesis

Abstract

Regioselective transformation is among the long-standing challenges in organic synthesis, particularly involving gas trapping. We present here a novel photocatalytic strategy for the regioselective carbonylation reaction toward α-aminoketones. Experimental studies reveal that protonic acids dissociated from protonated amines facilitate the reactions of low-reactive aldehydes and enhance the electrophilicity of imines, thereby promoting the efficient coupling of less nucleophilic acyl radicals. This approach introduces a reliable framework for controlling regioselectivity in photocatalytic multi-radical-coupled CO trapping reactions, broadens the chemical space of α-aminoketones, and advances carbonylation reactions for sustainable development.

Graphical abstract: Photocatalytic regioselective four-component radical relay carbonylation for α-aminoketones synthesis

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Article information

Article type
Edge Article
Submitted
06 Jun 2025
Accepted
16 Jul 2025
First published
05 Aug 2025
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2025, Advance Article

Photocatalytic regioselective four-component radical relay carbonylation for α-aminoketones synthesis

M. Yang and X. Wu, Chem. Sci., 2025, Advance Article , DOI: 10.1039/D5SC04120A

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