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 language | English |
|---|---|
| Pages (from-to) | 533-547 |
| Number of pages | 15 |
| Journal | Journal of Labelled Compounds and Radiopharmaceuticals |
| Volume | 21 |
| Issue number | 6 |
| DOIs | |
| State | Published - Jun 1984 |
| Externally published | Yes |
Keywords
- NCA Aryl F fluorides
- NCA [F]Fluorobenzene
- Nucleophilic substitution reaction
- [F]Benperidol
- [F]Spiroperidol
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