|
KMID : 1145520170030010003
|
|
Journal of Radiopharmaceuticals and Molecular Probes
2017 Volume.3 No. 1 p.3 ~ p.14
|
|
|
[18F]Aryl fluorides from hypervalent iodine compounds
|
|
Chun Joong-Hyun
Son Jeong-Min
Park Jun-Young
Yun Mi-Jin
|
|
|
Abstract
|
|
|
|
Nucleophilic aromatic fluorination has been one of the most explored methods in fluorin-18 based radiochemistry. Unlike electrophilic [18F]fluorination methods, no-carrier-added nucleophilic radiofluorination with cyclotronproduced [18F]fluoride ion offers better specific radioactivity which is essential aspect to obtain good quality images from positron emission tomography. Contrary to amenable aliphatic radiofluorination, the development of reliable aromatic [18F]fluorination methods has been pursued by many research groups; however, no viable method has yet been established. Recently, hypervalent iodine compound draws increasing attention as versatile radiolabeling precursor for various [18F]fluoroarenes, since it bears the capacity to introduce fluorine-18 either on electron-deficient or electron-rich aryl ring with enhanced regiospecificity. Other classes of hypervalent iodine congeners often utilized in radiochemistry are iodylarenes, iodonium ylides, and spirocyclic iodonium ylides. Recently developed spirocyclic iodonium ylides have already been avidly employed to provide various [18F]aryl fluorides with high labeling efficiency. This metal-free protocol would afford efficient routes, replacing the traditional approaches to [18F]fluoroarenes, from prosthetic labeling synthons to complex PET radiotracers.
|
|
|
KEYWORD
|
|
|
fluorine-18 , aromatic fluorination , hypervalent iodine , PET , radiotracer
|
|
|
FullTexts / Linksout information
|
|
|
|
|
|
Listed journal information
|
|
|
|