Stereostructure, conformation and reactivity of beta- and alpha-gardiol from Burchellia bubalina

Citation
Se. Drewes et al., Stereostructure, conformation and reactivity of beta- and alpha-gardiol from Burchellia bubalina, PHYTOCHEM, 50(3), 1999, pp. 387-394
Citations number
5
Categorie Soggetti
Agricultural Chemistry","Animal & Plant Sciences
Journal title
PHYTOCHEMISTRY
ISSN journal
00319422 → ACNP
Volume
50
Issue
3
Year of publication
1999
Pages
387 - 394
Database
ISI
SICI code
0031-9422(199902)50:3<387:SCAROB>2.0.ZU;2-J
Abstract
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 98 Elsevier Science Ltd. All rights reserved.