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
Hauptverfasser: Drewes, S.E, Horn, M.M, Munro, O.Q, Ramesar, N, Ochse, M, Bringmann, G, Peters, K, Peters, E.M
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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.
ISSN:0031-9422
1873-3700
DOI:10.1016/S0031-9422(98)00508-1