Radical fluoroarylation in radiochemical synthesis |
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Authors: | Christina Hultsch,Hans-Jü rgen Wester |
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Affiliation: | a Nuklearmedizinische Klinik und Poliklinik, Klinikum Rechts der Isar, Technische Universität München, Germany b Organische Chemie 1, Technische Universität München, Lichtenbergstr. 4, D-85747 Garching, Germany |
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Abstract: | In this study, we report on the radical [18F]fluoroarylation of different olefins using 4-[18F]fluorobenzenediazonium ions to provide a new route to radiopharmaceuticals containing a deactivated, 4-[18F]fluoro substituted phenyl group. This new methodology was shown to be well suited for the synthesis of 18F-labelled stilbenes. Stilbene 7 is now accessible within 80 min in 30-45% overall radiochemical yield starting from [18F]fluoride. |
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