Recent Advances in F-18 Radiochemistry: A Focus on B-F-18, Si-F-18, Al-F-18, and C-F-18 Radiofluorination via Spirocyclic Iodonium Ylides

摘要

Straightforward radiosynthesis protocols for F-18-labeled radio-pharmaceuticals 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 F-18 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 F-18-labeling methodologies, specifically for B-F-18, Si-F-18, Al-F-18, and iodine (III)-mediated radio-fluorination via the spirocyclic iodonium ylide technology.