Stereoselective synthesis of 3-O-methyl-6-[18F]fluorodopa via fluorodestannylation

DOI: 10.1002/jlcr.2580340611

Source and publish data:

Journal of labelled compounds and radiopharmaceuticals p. 565 - 570 (1994)

Update date:2022-08-05

Topics: Stereoselective synthesis Experimental terms

Authors:

Adam Adam

Jivan Jivan

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Article abstract of DOI:10.1002/jlcr.2580340611

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.

Full text of DOI:10.1002/jlcr.2580340611

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