Issue 89, 2019

Rhodium-mediated 18F-oxyfluorination of diazoketones using a fluorine-18-containing hypervalent iodine reagent

Abstract

Geminal 18F-oxyfluorination of diazoketones was performed in the presence of rhodium mediators. The reactions were performed using a hypervalent iodine-based [18F]fluoro-benziodoxole reagent. By this methodology various α-[18F]fluoro ethers were obtained in high radiochemical yield (up to 98%) and molar activity (216 GBq μmol−1).

Graphical abstract: Rhodium-mediated 18F-oxyfluorination of diazoketones using a fluorine-18-containing hypervalent iodine reagent

Supplementary files

Article information

Article type
Communication
Submitted
04 Sep 2019
Accepted
10 Oct 2019
First published
11 Oct 2019
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2019,55, 13358-13361

Rhodium-mediated 18F-oxyfluorination of diazoketones using a fluorine-18-containing hypervalent iodine reagent

M. A. Cortés González, X. Jiang, P. Nordeman, G. Antoni and K. J. Szabó, Chem. Commun., 2019, 55, 13358 DOI: 10.1039/C9CC06905D

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