Royal Society of Chemistry, Organic and Biomolecular Chemistry, 38(17), p. 8701-8705, 2019
DOI: 10.1039/c9ob01758e
Full text: Unavailable
A one-pot two-step synthesis of 6-[18F]fluoro-l-DOPA has been developed, involving Cu-mediated radiofluorination of the corresponding pinacol boronate ester precursor, and validated for production of doses for human use.