Issue 47, 2024

Visible-light photoredox-catalyzed three-component radical alkyl-acylation of [1.1.1]propellane

Abstract

We described herein a three-component radical alkyl-acylation of [1.1.1]propellane via a visible-light photoredox single electron transfer process, demonstrating an efficient approach for accessing a diverse array of 1,3-disubstituted BCP ketone derivatives. The synthetic utility of the present radical protocol was further demonstrated by the Baeyer–Villiger oxidation of the BCP ketone for BCP ester formation.

Graphical abstract: Visible-light photoredox-catalyzed three-component radical alkyl-acylation of [1.1.1]propellane

Supplementary files

Article information

Article type
Communication
Submitted
23 Sep 2024
Accepted
22 Oct 2024
First published
22 Oct 2024

Org. Biomol. Chem., 2024,22, 9192-9196

Visible-light photoredox-catalyzed three-component radical alkyl-acylation of [1.1.1]propellane

L. Liu, S. Guo, C. Chen, X. Shen, X. Chen, H. Yu, Y. Han, Q. Sun, S. Zhu and H. Hou, Org. Biomol. Chem., 2024, 22, 9192 DOI: 10.1039/D4OB01549E

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