A synthetic approach to carbon-14 labeled anti-bacterial napthyridine and quinolone carboxylic acids
Labeled versions of (S)‐clinafloxacin (1) and two naphthyridine carboxylic acid anti‐bacterial compounds 2 and 3 which are currently in development were synthesized. Preparations started from hitherto unknown bromo compounds 22 and 10, from which the corresponding 14C‐labeled aromatic carboxylic aci...
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Veröffentlicht in: | Journal of labelled compounds & radiopharmaceuticals 1993-09, Vol.33 (9), p.869-880 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Labeled versions of (S)‐clinafloxacin (1) and two naphthyridine carboxylic acid anti‐bacterial compounds 2 and 3 which are currently in development were synthesized. Preparations started from hitherto unknown bromo compounds 22 and 10, from which the corresponding 14C‐labeled aromatic carboxylic acids 23 and 12 were generated by metal‐halogen exchange followed by carboxylation reaction. Details of these preparations are given. |
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ISSN: | 0362-4803 1099-1344 |
DOI: | 10.1002/jlcr.2580330911 |