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Selective syntheses of no-carrier-added 2- and 3-[~(18)F]fluorohalopyridines through the radiofluorination of halopyridinyl(4'-methoxy phenyl)iodonium tosylates

机译:通过卤代吡啶基(4'-甲氧基苯基)碘代甲苯磺酸盐的放射性氟化选择性合成无载体的2-和3- [〜((18)F]氟卤代吡啶

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摘要

No-carrier-added 2- and 3-[~(18)F]fluorohalopyridines were readily synthesized as potentially useful labeling synthons for prospective PET radiotracers through the selective radiofluorination of halopyridinyl(4'-methoxyphenyl)iodonium tosylates, themselves conveniently prepared in a single pot from iodohalopyridines.
机译:通过卤代吡啶基(4'-甲氧基苯基)碘代甲苯磺酸盐的选择性放射性氟化,可以方便地合成无载体的2-和3- [〜(18)F]氟卤代吡啶,它们可能对潜在的PET放射性示踪剂有用。从碘卤吡啶中取出一锅。

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    《Chemical Communications》 |2012年第79期|p.9921-9923|共3页
  • 作者单位

    Molecular Imaging Branch, National Institute of Mental Health, National Institutes of Health, Building 10, Room B3 C346A, 10 Center Drive, Bethesda, MD 20892-1003, USA;

    Molecular Imaging Branch, National Institute of Mental Health, National Institutes of Health, Building 10, Room B3 C346A, 10 Center Drive, Bethesda, MD 20892-1003, USA;

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