A new eremophilanolide from Senecio sinuatus Gilib

Copyright 2007 John Wiley & Sons, Ltd.

Bibliographische Detailangaben
Veröffentlicht in:Magnetic resonance in chemistry : MRC. - 1985. - 45(2007), 6 vom: 15. Juni, Seite 457-62
1. Verfasser: Burgueño-Tapia, Eleuterio (VerfasserIn)
Weitere Verfasser: López-Escobedo, Susana, González-Ledesma, Manuel, Joseph-Nathan, Pedro
Format: Aufsatz
Sprache:English
Veröffentlicht: 2007
Zugriff auf das übergeordnete Werk:Magnetic resonance in chemistry : MRC
Schlagworte:Journal Article Research Support, Non-U.S. Gov't 3beta-angeloyloxy-6beta-hydroxyeremophil-1(10)-en-8beta,12-olide Carbon Isotopes Hexanes Sesquiterpenes Solvents Triterpenes eremophilenolide Hydrogen 7YNJ3PO35Z
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520 |a From the hexane extracts of Senecio sinuatus roots, the new 3beta-angeloyloxy-6beta-hydroxyeremophil-1(10)-en-8beta,12-olide (3), along with the known compounds 3beta-angeloyloxy-6beta-hydroxyeremophil-1(10)-ene (1), 3beta-senecioyloxy-6beta-hydroxyeremophil-1(10)-ene (2), and 3beta-angeloyloxy-6beta,8alpha-dihydroxyeremophil-1(10)-en-8beta,12-olide (4), were isolated. Complete 1H and 13C NMR chemical shift assignments of 1-4 were achieved using one- and two-dimensional NMR techniques, including gHMQC and gHMBC experiments. A Monte Carlo search, followed by B3LYP/6-31G*DFT calculation, provided the theoretical conformations of the eremophilane rings, which were in agreement with results derived from 1H-1H NMR coupling constant analysis, and confirmed by NOESY experiments 
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700 1 |a López-Escobedo, Susana  |e verfasserin  |4 aut 
700 1 |a González-Ledesma, Manuel  |e verfasserin  |4 aut 
700 1 |a Joseph-Nathan, Pedro  |e verfasserin  |4 aut 
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