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 |
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Hauptverfasser: | , , , |
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. |
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ISSN: | 0362-4803 1099-1344 |
DOI: | 10.1002/jlcr.4073 |