2000
DOI: 10.1246/bcsj.73.417
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Synthesis of a Chiral Precursor for No-Carrier-Added (NCA) PET Tracer 6-[18F]Fluoro-L-dopa Based on Regio- and Enantioselective Alkylation of 2,4-Bis(chloromethyl)-5-iodoanisole

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Cited by 5 publications
(1 citation statement)
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“…Kuroda et al (17) described the synthesis of a similar precursor with this strategy by choosing a homochiral imidazolidinone derivative (according to Seebach et al (18)) as the masked amino acid functionality and iodide as the leaving group in the formyl-activated 18 F exchange reaction. Unfortunately, no 18 F-labeling results with this precursor have been reported so far.…”
mentioning
confidence: 99%
“…Kuroda et al (17) described the synthesis of a similar precursor with this strategy by choosing a homochiral imidazolidinone derivative (according to Seebach et al (18)) as the masked amino acid functionality and iodide as the leaving group in the formyl-activated 18 F exchange reaction. Unfortunately, no 18 F-labeling results with this precursor have been reported so far.…”
mentioning
confidence: 99%