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Synthesis of 18F-Labeled Aryl Fluorosulfates via Nucleophilic Radiofluorination.
Kwon, Young-Do; Jeon, Min Ho; Park, Nam Kyu; Seo, Jeong Kon; Son, Jeongmin; Ryu, Young Hoon; Hong, Sung You; Chun, Joong-Hyun.
Afiliação
  • Kwon YD; Department of Nuclear Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
  • Jeon MH; Department of Chemistry, School of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea.
  • Park NK; Department of Chemistry, School of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea.
  • Seo JK; UNIST Central Research Facility, Ulsan 44919, Republic of Korea.
  • Son J; Department of Nuclear Medicine, Yonsei University Health System, Seoul 03722, Republic of Korea.
  • Ryu YH; Department of Nuclear Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
  • Hong SY; Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul 06273, Republic of Korea.
  • Chun JH; Department of Chemistry, School of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea.
Org Lett ; 22(14): 5511-5516, 2020 07 17.
Article em En | MEDLINE | ID: mdl-32589035
ABSTRACT
Sulfuryl fluoride gas is a key reagent for SO2F transfer. However, conventional SO2F transfer reactions have limited 18F-radiochemistry translation, due to the inaccessibility of gaseous [18F]SO2F2. Herein, we report the first SO2F2-free synthesis of aryl [18F]fluorosulfates from both phenolic and isolated aryl imidazylate precursors with cyclotron-produced 18F-. The radiochemical yields ranged from moderate to good with excellent functional group tolerance. The reliability of our approach was validated by the automated radiosynthesis of 4-acetamidophenyl [18F]fluorosulfate.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article