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Herein, we disclose that pyridinium salts derived from abundant (hetero)anilines represent a novel precursor class for nucleophilic aromatic substitution reactions with [18F]fluoride. The value of this new 18F-fluorodeamination is demonstrated with the synthesis of over 30 structurally diverse and complex heteroaryl 18F-fluorides, several derived from scaffolds that were yet to be labelled with fluorine-18. The protocol tolerates heteroarenes and functionalities commonly found in drug discovery libraries, and is amenable to scale-up and automation on a commercial radiosynthesiser.

Original publication

DOI

10.1002/anie.202404945

Type

Journal article

Journal

Angew Chem Int Ed Engl

Publication Date

16/04/2024

Keywords

Fluorine, Heterocycles, Nucleophilic substitution, Radiochemistry, Radiopharmaceuticals