Royal Society of Chemistry, Chemical Communications, 45(55), p. 6361-6364, 2019
DOI: 10.1039/c9cc02779c
Full text: Unavailable
This report describes a simple technique for the preparation of [18F]HF and its application to the generation of an [18F]FeF species for opening sterically hindered epoxides. This easily automated one-pot procedure has been successfully employed to prepare four drug-like molecules in good yields and high molar activities, including 5-[18F]fluoro-6-hydroxy-cholesterol.