Issue 48, 2025

Synthesis of phenolic derivatives via photoredox formal [4 + 2] tandem annulation of α-bromoketones and terminal alkynes

Abstract

A photoredox formal [4 + 2] cycloaddition reaction has been developed, which directly utilizes commercially available and affordable α-bromoketones and terminal alkynes to produce naphthol derivatives in a single step. This method features mild reaction conditions and straightforward operation. The naphthol derivatives obtained can be easily transformed into 4-substituted naphthols, 3-substituted benzofurans, and imidazo heterocycles.

Graphical abstract: Synthesis of phenolic derivatives via photoredox formal [4 + 2] tandem annulation of α-bromoketones and terminal alkynes

Supplementary files

Article information

Article type
Communication
Submitted
08 Oct 2025
Accepted
18 Nov 2025
First published
19 Nov 2025

Org. Biomol. Chem., 2025,23, 10857-10862

Synthesis of phenolic derivatives via photoredox formal [4 + 2] tandem annulation of α-bromoketones and terminal alkynes

Y. Ma, P. Yu, G. Shang, J. Hu, Z. Zhang, L. Shi, Q. Chang, S. Sun and D. Liang, Org. Biomol. Chem., 2025, 23, 10857 DOI: 10.1039/D5OB01596K

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