Issue 1, 2025

Cooperative photoredox and N-heterocyclic carbene-catalyzed formal C–H acylation of cyclopropanes via a deconstruction–reconstruction strategy

Abstract

Cyclopropanes are ubiquitous and key structural motifs in commercially available drugs and bioactive molecules. Herein, we present regio-selective acylation of aryl cyclopropanes with cooperative photoredox and N-heterocyclic carbene catalysis. This approach involves a deconstruction–reconstruction strategy via γ-chloro-ketones as intermediates and fulfills the formal C(sp3)–H functionalization of cyclopropanes.

Graphical abstract: Cooperative photoredox and N-heterocyclic carbene-catalyzed formal C–H acylation of cyclopropanes via a deconstruction–reconstruction strategy

Supplementary files

Article information

Article type
Edge Article
Submitted
19 Sep 2024
Accepted
21 Nov 2024
First published
22 Nov 2024
This article is Open Access

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

Chem. Sci., 2025,16, 323-328

Cooperative photoredox and N-heterocyclic carbene-catalyzed formal C–H acylation of cyclopropanes via a deconstruction–reconstruction strategy

F. Gao, T. Wang and X. Yan, Chem. Sci., 2025, 16, 323 DOI: 10.1039/D4SC06355D

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