Issue 80, 2024

Photo-induced difluoroalkylation/cyclization of alkyne ketones: a novel strategy to access difluoroalkyl thiofavones

Abstract

A photo-induced electron donor–acceptor (EDA) complex enabled tandem reaction of alkyne ketones via a radical difluoroalkylation/cyclization cascade sequence is reported. The EDA complex plays a key role, and the CBr bond homolysis process may also be involved for this transformation. Varieties of difluoroalkyl-substituted thiofavones can be smoothly assembled in moderate to good yields under photocatalyst-, metal- and oxidant-free conditions, thus offering potential applications for pharmaceutical research.

Graphical abstract: Photo-induced difluoroalkylation/cyclization of alkyne ketones: a novel strategy to access difluoroalkyl thiofavones

Supplementary files

Article information

Article type
Communication
Submitted
30 Jul 2024
Accepted
11 Sep 2024
First published
12 Sep 2024

Chem. Commun., 2024,60, 11323-11326

Photo-induced difluoroalkylation/cyclization of alkyne ketones: a novel strategy to access difluoroalkyl thiofavones

S. Song, C. Luo, G. Wang, J. Guo, Z. Chen and J. Li, Chem. Commun., 2024, 60, 11323 DOI: 10.1039/D4CC03843F

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