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Progress in [18F]Fluorination by Using Aryliodonium(III) Compounds and Application for PET Tracer Syntheses

Journal

MINI-REVIEWS IN ORGANIC CHEMISTRY
Volume 18, Issue 2, Pages 173-195

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1570193X17999200629155733

Keywords

[F-18]fluorine; aryliodonium compound; fluoroarene; late-stage fluorination; PET imaging; radiosynthesis

Funding

  1. JSPS [18H02014, 19K05466]
  2. Ritsumeikan Global Innovation Research Organization (R-GIRO) project
  3. Ritsumeikan University, Japan
  4. Grants-in-Aid for Scientific Research [19K05466, 18H02014] Funding Source: KAKEN

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The use of [F-18]-labeled drugs and radioligands is common in PET radiopharmaceuticals for clinical and preclinical research. Various methods for introducing [F-18]fluorine into complex molecules through fluorination reactions have been reported. Recent advances in [F-18]-fluorination using aryliodonium(III) compounds are highlighted in this study.
[F-18]-labeled drugs and radioligands are most frequently used in positron-emission tomography (PET) radiopharmaceuticals for both clinical and preclinical research. Various methods for the introduction of [F-18]fluorine into complex molecules through fluorination reactions have been reported. Herein, recent advances in [F-18]-fluorination utilizing aryliodonium(III) compounds are high-lighted.

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