4.4 Article

Nucleophilic 18F-Fluorination of Anilines via N-Arylsydnone Intermediates

期刊

SYNLETT
卷 29, 期 9, 页码 1131-1135

出版社

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0036-1591948

关键词

fluorine-18; sydnone; bioorthogonal chemistry; fluoroarene; peptide labeling

资金

  1. Jonsson Comprehensive Cancer Center
  2. Crump Institute for Molecular Imaging
  3. NIH [R01GM109078]
  4. FRQNT

向作者/读者索取更多资源

Preparation of [F-18]fluoroarenes with nucleophilic [F-18]fluoride for positron emission tomography (PET) molecular imaging research is a challenging chemical endeavor. Advances in radiofluorination have soared in the last decade, broadening the availability of potential [F-18]fluoroarenes. In this Synpacts article, we highlight the recent development from our laboratory of a practical radiofluorination of anilines via N-arylsydnone intermediates to afford [F-18]fluoroarenes. Further, we emphasize the utility of this methodology towards peptide labeling applications by preparing an F-18-labeled neuropeptide. 1 Introduction 2 Nucleophilic Radiofluorination of N-Arylsydnones 3 Substrate Scope and Applications 4 Conclusion

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