Journal of labelled compounds and radiopharmaceuticals p. 565 - 570 (1994)
Update date:2022-08-05
Topics: Stereoselective synthesis Experimental terms 3-O-methyl-6-[18F]fluorodopa Fluorodestannylation 18F
Adam
Lu
Jivan
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.
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