Stereostructure, conformation and reactivity of beta- and alpha-gardiol from Burchellia bubalina
From the leaves of Burchellia bubalina (Rubiaceae) pure beta- and alpha-gardiol have been isolated, the latter in crystalline form for the first time. X-ray analysis of beta-gardiol establishes its relative configuration. Treatment of the tosyl derivative of beta-gardiol with base affords a crystall...
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Veröffentlicht in: | Phytochemistry (Oxford) 1999-02, Vol.50 (3), p.387-394 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | From the leaves of Burchellia bubalina (Rubiaceae) pure beta- and alpha-gardiol have been isolated, the latter in crystalline form for the first time. X-ray analysis of beta-gardiol establishes its relative configuration. Treatment of the tosyl derivative of beta-gardiol with base affords a crystalline elimination product amenable to X-ray analysis. Evidence is presented for the partial conversion of alpha-gardiol to the epimeric beta-gardiol at room temperature. Molecular dynamic studies at 1000 K on the two gardiols provide useful conformational information. In the case of beta-gardiol, the analysis shows interesting correlations between conformations adopted at 1000 K and those present in the crystalline state at room temperature. |
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ISSN: | 0031-9422 1873-3700 |
DOI: | 10.1016/S0031-9422(98)00508-1 |