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- W2015016503 abstract "3-O-Methyl-2- and 6-[18F]-fluorodopa were synthesized in 8% radiochemical yield by the direct fluorination of a protected L-dopa derivative with [18F]-acetyl hypofluorite. The 2- and 6-fluoro isomers were separated and purified by reverse phase HPLC." @default.
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- W2015016503 title "Synthesis and separation of 3-O-Methyl-2- and 6-[18F]-fluorodopa" @default.
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- W2015016503 doi "https://doi.org/10.1002/jlcr.2580310106" @default.
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