Issue 76, 2024

Borate-mediated aryl polyfluoroalkoxylation under transition-metal-free conditions

Abstract

We describe the transition-metal-free coupling for polyfluoroalkoxy arenes using polyfluoroalkoxy borates, which serve as counterions to diaryliodonium salts and transferring mediators of polyfluoroalkoxy groups. This strategy demonstrates high functional group compatibility owing to the low nucleophilicity of the borate mediator, thus offering a practical approach for synthesizing diverse polyfluoroalkoxy arenes.

Graphical abstract: Borate-mediated aryl polyfluoroalkoxylation under transition-metal-free conditions

Supplementary files

Article information

Article type
Communication
Submitted
07 Aug 2024
Accepted
26 Aug 2024
First published
29 Aug 2024

Chem. Commun., 2024,60, 10552-10555

Borate-mediated aryl polyfluoroalkoxylation under transition-metal-free conditions

K. Kikushima, T. Tsuda, N. Miyamoto, Y. Kita and T. Dohi, Chem. Commun., 2024, 60, 10552 DOI: 10.1039/D4CC04008B

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