Se. Drewes et al., Stereostructure, conformation and reactivity of beta- and alpha-gardiol from Burchellia bubalina, PHYTOCHEM, 50(3), 1999, pp. 387-394
From the leaves of Burchellia bubalina (Rubiaceae) pure beta- and alpha-gar
diol have been isolated, the latter in crystalline form for the first time.
X-ray analysis of beta-gardiol establishes its relative configuration. Tre
atment of the tosyl derivative of beta-gardiol with base affords a crystall
ine elimination product amenable to X-ray analysis. Evidence is presented f
or the partial conversion of alpha-gardiol to the epimeric beta-gardiol at
room temperature. Molecular dynamic studies at 1000 K on the two gardiols p
rovide useful conformational information. In the case of beta-gardiol, the
analysis shows interesting correlations between conformations adopted at 10
00 K and those present in the crystalline state at room temperature. (C) 19
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