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Application of the nucleophilic substitution reaction to the synthesis of No‐carrier‐added [18F]fluorobenzene and other 18F‐labeled aryl fluorides

  • C. ‐Y Shiue
  • , M. Watanabe
  • , A. P. Wolf
  • , J. S. Fowler
  • , P. Salvadori

Research output: Contribution to journalArticlepeer-review

52 Scopus citations

Abstract

No‐carrier‐added (NCA) [18F]fluorobenzene was prepared in a multistep synthesis with a radiochemical yield of 20‐30%. A series of NCA and CA 18F‐labeled aryl fluorides which are important precursors of 18F‐labeled butyrophenone neuroleptics have also been synthesized in radiochemical yields of 30–50%. The direct synthesis of [18F]spiroperidol and [18F]benperidol from the parent compounds and/or nitro and/or chloro compound using the nucleophilic substitution reactions were also investigated.

Original languageEnglish
Pages (from-to)533-547
Number of pages15
JournalJournal of Labelled Compounds and Radiopharmaceuticals
Volume21
Issue number6
DOIs
StatePublished - Jun 1984
Externally publishedYes

Keywords

  • NCA Aryl F fluorides
  • NCA [F]Fluorobenzene
  • Nucleophilic substitution reaction
  • [F]Benperidol
  • [F]Spiroperidol

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