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Ring-Closing Synthesis of Dibenzothiophene Sulfonium Salts and Their Use as Leaving Groups for Aromatic 18F-Fluorination.
Gendron, Thibault; Sander, Kerstin; Cybulska, Klaudia; Benhamou, Laure; Sin, Pak Kwan Brian; Khan, Aqsa; Wood, Michael; Porter, Michael J; Årstad, Erik.
Afiliação
  • Gendron T; Institute of Nuclear Medicine , University College London , 235 Euston Road (T-5) , London NW1 2BU , United Kingdom.
  • Sander K; Department of Chemistry , University College London , 20 Gordon Street , London WC1H 0AJ , United Kingdom.
  • Cybulska K; Institute of Nuclear Medicine , University College London , 235 Euston Road (T-5) , London NW1 2BU , United Kingdom.
  • Benhamou L; Department of Chemistry , University College London , 20 Gordon Street , London WC1H 0AJ , United Kingdom.
  • Sin PKB; Department of Chemistry , University College London , 20 Gordon Street , London WC1H 0AJ , United Kingdom.
  • Khan A; Institute of Nuclear Medicine , University College London , 235 Euston Road (T-5) , London NW1 2BU , United Kingdom.
  • Wood M; Department of Chemistry , University College London , 20 Gordon Street , London WC1H 0AJ , United Kingdom.
  • Porter MJ; Institute of Nuclear Medicine , University College London , 235 Euston Road (T-5) , London NW1 2BU , United Kingdom.
  • Årstad E; Department of Chemistry , University College London , 20 Gordon Street , London WC1H 0AJ , United Kingdom.
J Am Chem Soc ; 140(35): 11125-11132, 2018 09 05.
Article em En | MEDLINE | ID: mdl-30132661
ABSTRACT
Herein, we report a novel intramolecular ring-closing reaction of biaryl thioethers that give access to highly functionalized dibenzothiophene sulfonium salts under mild conditions. The resulting precursors react regioselectively with [18F]fluoride to give [18F]fluoroarenes in predictable radiochemical yields. The strategy expands the available radiochemical space and provides superior labeling efficiency for clinically relevant PET tracers.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Reino Unido