Dehydrobrachylaenolide : an eudesmanetype sesquiterpene lactone
dc.contributor.author | Rademeyer, Melanie | |
dc.contributor.author | Van Heerden, Fanie R. | |
dc.contributor.author | Van der Merwe, Marina M. | |
dc.contributor.email | melanie.rademeyer@up.ac.za | en_US |
dc.date.accessioned | 2009-11-25T10:07:29Z | |
dc.date.available | 2009-11-25T10:07:29Z | |
dc.date.issued | 2009 | |
dc.description.abstract | The three-ring eudesmanolide, C15H16O3, is a natural product isolated from Dicoma anomala Sond. (Asteraceae). The compound contains an endo–exo cross conjugated methylenecyclohexenone ring with an envelope conformation transfused with cyclohexane and trans-annelated with an - methylene -lactone. The absolute structure was assigned by optical rotation measurements compared to those from the synthetic compound with known stereochemistry. The crystal packing is consolidated by C—H...O interactions. | en_US |
dc.description.sponsorship | National Drug Development Platform NDDP) and the NRF. | en_US |
dc.identifier.citation | Rademeyer, M, Van Heerden, FR & Van Der Merwe, MM 2009, 'Dehydrobrachylaenolide: an eudesmanetype sesquiterpene lactone', Acta Crystallographica, E65, p. 196. [http://journals.iucr.org/e/journalhomepage.html] | en_US |
dc.identifier.issn | 1600-5368 | |
dc.identifier.other | 10.1107/S1600536808042402 | |
dc.identifier.uri | http://hdl.handle.net/2263/12038 | |
dc.language.iso | en | en_US |
dc.publisher | International Union of Crystallography | en_US |
dc.rights | International Union of Crystallography | en_US |
dc.subject | Single-crystal X-ray study | en |
dc.subject | T = 150 K | en |
dc.subject | Mean (C–C) = 0.002 A° | en |
dc.subject | R factor = 0.033 | en |
dc.subject | wR factor = 0.095 | en |
dc.subject | Data-to-parameter ratio = 14.1 | en |
dc.subject.lcsh | Lactones | en |
dc.subject.lcsh | Stereochemistry | en |
dc.title | Dehydrobrachylaenolide : an eudesmanetype sesquiterpene lactone | en_US |
dc.type | Article | en_US |