ChemInform Abstract: Design, Synthesis and Inhibitory Activity Against Mycobacterium tuberculosis Thymidine Monophosphate Kinase of Acyclic Nucleoside Analogues with a Distal Imidazoquinolinone
New acyclic analogues, structurally related to previously described acyclic nucleoside inhibitors, are synthesized via PIFA‐mediated electrocyclization of N‐methoxyureas, e.g. (V), followed by elimination of the methoxy groups by catalytic hydrogenation.
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Veröffentlicht in: | ChemInform 2011-04, Vol.42 (14), p.no-no |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | New acyclic analogues, structurally related to previously described acyclic nucleoside inhibitors, are synthesized via PIFA‐mediated electrocyclization of N‐methoxyureas, e.g. (V), followed by elimination of the methoxy groups by catalytic hydrogenation. |
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ISSN: | 0931-7597 1522-2667 |
DOI: | 10.1002/chin.201114207 |