Visible-light-mediated radical difunctionalization of alkenes with aromatic aldehydes

Abstract

We have developed a visible-light-mediated three-component tandem reaction of aromatic aldehydes with acrylates using a Hantzsch ester as the hydrogen atom transfer reagent, generating diethyl pentanedioate products in a one-pot synthesis. The reaction facilitates direct formation of acyl groups from the corresponding aldehydes, which are subsequently coupled successively to two molecules of acrylate in a Giese addition.

Graphical abstract: Visible-light-mediated radical difunctionalization of alkenes with aromatic aldehydes

Supplementary files

Article information

Article type
Communication
Submitted
27 Dec 2024
Accepted
12 Feb 2025
First published
13 Feb 2025

Org. Biomol. Chem., 2025, Advance Article

Visible-light-mediated radical difunctionalization of alkenes with aromatic aldehydes

Z. Xu, T. Geng, J. Du, Y. Zuo, X. Hu, L. Liu, Z. Shi and H. Huang, Org. Biomol. Chem., 2025, Advance Article , DOI: 10.1039/D4OB02090A

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