## Abstract Compared to homoaromatic and aliphatic nucleophilic radiofluorinations, only few references can be found in the literature describing nucleophilic substitutions with [^18^F]fluoride ion of heteroaromatic compounds such as pyridines and only reactions involving fluorination processes at
Mechanistic approach of the nucleophilic18F- exchange on 4′-NO2-spiperone using TBA18F or K2.2.2./K18F
✍ Scribed by M. Gysemans; J. Mertens
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- French
- Weight
- 356 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
High yield single step preparation of 4′‐^18^F‐spiperone by ^18^F‐ for NO~2~ exchange in highly basic conditions fails when using 4′‐NO~2~‐spiperone as a precursor. This compound moreover inhibits radiofluorination of highly activated molecules in mentioned conditions. Inhibition is not provoced by ketalised analogues of the butyrophenone. This led to assume that enolisation of the butyrophenone was responsible for those phenomena. The assumption is supported by the fact that the results of inhibition experiments fit to a theoretical model.
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