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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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