Preparation of 6‐azauracil‐5‐ 3 H and 6‐azauridine‐5‐ 3 H of high molar activity
Catalytic reductive dehalogenation of 5‐bromo‐6‐azauracil with carrier‐free tritium led to 6‐azauracil‐5‐ 3 H of a molar activity of 19.0 Ci/mmole. The reaction conditions for the catalytic reductive dehalogenation were examined in tracer experiments. Microbial transformation was used for the prepar...
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Veröffentlicht in: | Journal of labelled compounds 1974-01, Vol.10 (1), p.59-71 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Catalytic reductive dehalogenation of 5‐bromo‐6‐azauracil with carrier‐free tritium led to 6‐azauracil‐5‐
3
H of a molar activity of 19.0 Ci/mmole. The reaction conditions for the catalytic reductive dehalogenation were examined in tracer experiments. Microbial transformation was used for the preparation of 6‐azauridine‐5‐
3
H from 6‐azauracil‐5‐
3
H. 6‐Azauridine‐5‐
3
‐ H was prepared at a molar activity of 18.8 Ci/mmole. In both compounds the stability of tritium was investigated in an aqueous medium at 100°C. |
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ISSN: | 0022-2135 |
DOI: | 10.1002/jlcr.2590100108 |