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Royal Society of Chemistry, Organic and Biomolecular Chemistry, 38(17), p. 8701-8705, 2019

DOI: 10.1039/c9ob01758e

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One-pot synthesis of high molar activity 6-[18F]fluoro-l-DOPA by Cu-mediated fluorination of a BPin precursor

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

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.