期刊
JOURNAL OF NUCLEAR MEDICINE
卷 59, 期 4, 页码 568-572出版社
SOC NUCLEAR MEDICINE INC
DOI: 10.2967/jnumed.117.197095
关键词
radiochemistry; fluorine-18; radiofluorination; spirocyclic iodonium
Straightforward radiosynthesis protocols for F-18-labeled radio-pharmaceuticals are an indispensable but often overlooked prerequisite to successfully perform molecular imaging studies in vivo by PET. In recent years, thanks to the expansion of the F-18 chemical toolbox, structurally diverse and novel clinically relevant radiopharmaceuticals have been synthesized with both high efficiency and ready implementation. This article provides an overview of recent F-18-labeling methodologies, specifically for B-F-18, Si-F-18, Al-F-18, and iodine (III)-mediated radio-fluorination via the spirocyclic iodonium ylide technology.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据