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Straightforward radiosynthesis protocols for ¹⁸F-labeled radiopharmaceuticals are an indispensable but often overlooked prerequisite to successfully perform molecular imaging studies in vivo by PET. In recent years, thanks to the expansion of the ¹⁸F chemical toolbox, structurally diverse and novel clinically relevant radiopharmaceuticals have been synthesized with both high efficiency and ready implementation. This article provides an overview of recent ¹⁸F-labeling methodologies, specifically for B-¹⁸F, Si-¹⁸F, Al-¹⁸F, and iodine (III)-mediated radiofluorination via the spirocyclic iodonium ylide technology.
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Bernard‐Gauthier et al. (2017) studied this question.
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