72683-85-3Relevant academic research and scientific papers
Stereoselective synthesis of 3-O-methyl-6-[18F]fluorodopa via fluorodestannylation
Adam,Lu,Jivan
, p. 565 - 570 (1994)
3-O-Methyl-6-[18F]fluorodopa was synthesized in 20% radiochemical yield in 60 min, with a specific activity of 500 mCi/mmol, by the fluorination of a stannylated dopa precursor with [18F]-acetyl hypofluorite.
