Photocatalyzed radiosynthesis of 11 C-phenylacetic acids

Fast and straightforward incorporation of radionuclides into pharmaceutically relevant molecules is one of the main barriers to preclinical and clinical tracer research. Late-stage direct incorporation of cyclotron-produced [ C]CO to afford carbon-11-labeled radiopharmaceuticals has the potential to...

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Veröffentlicht in:Journal of labelled compounds & radiopharmaceuticals 2024-05, Vol.67 (6), p.211-216
Hauptverfasser: Munch, Maxime, Mair, Braeden A, Adi, Myriam, Rotstein, Benjamin H
Format: Artikel
Sprache:eng
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Zusammenfassung:Fast and straightforward incorporation of radionuclides into pharmaceutically relevant molecules is one of the main barriers to preclinical and clinical tracer research. Late-stage direct incorporation of cyclotron-produced [ C]CO to afford carbon-11-labeled radiopharmaceuticals has the potential to provide ready-to-inject positron emission tomography agents in less than an hour. The present work describes photocatalyzed carboxylation of alkylbenzene derivatives to afford C-phenylacetic acids. Reaction conditions and scope are investigated followed by application of this methodology to the preparative radiosynthesis of [ C]fenoprofen, a nonsteroidal anti-inflammatory drug.
ISSN:0362-4803
1099-1344
DOI:10.1002/jlcr.4073