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dc.creatorBrito, Iván
dc.creatorBorquez, Jorge
dc.creatorHuarote, Emily
dc.creatorLoyola, Luis
dc.creatorCárdenas, Alejandro
dc.creatorSimirgiotis, Mario
dc.date2017-09-02
dc.date.accessioned2019-11-13T15:11:37Z
dc.date.available2019-11-13T15:11:37Z
dc.identifierhttp://www.jcchems.com/index.php/JCCHEMS/article/view/330
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/112633
dc.descriptionThe structure of this mulinolic acid consists of a mulinane skeleton and the corresponding isopropyl, methyl, carboxyl and methyl groups at C3, C8, C5, C13, respectively, which are β-oriented, whereas the hydroxyl group at C13 is α-oriented. The cyclopentane (A), ciclohexane (B) and cicloheptene (C) rings are trans (A/B) and (B/C) cis fused, and in an envelope, chair, and twist conformation respectively.In the crystal the molecules are linked by two intermolecular O-H⋅⋅⋅O hydrogen bond forming bidimensional supramolecular structures with graph-set notation R44(12), R44(40), R66(46) and C44(46). The absolute configuration of the title compound has been determined from the refinement of the Flack parameter16. On this basis the absolute configuration was assigned as C3R, C5S, C8S, C9S, C10S and C13R.en-US
dc.formatapplication/pdf
dc.languageeng
dc.publisherSociedad Chilena de Químicaen-US
dc.relationhttp://www.jcchems.com/index.php/JCCHEMS/article/view/330/187
dc.rightsCopyright (c) 2017 Journal of the Chilean Chemical Societyen-US
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/4.0en-US
dc.sourceJournal of the Chilean Chemical Society; Vol 62 No 3 (2017): Journal of the Chilean Chemical Societyen-US
dc.source0717-9707
dc.source0717-9324
dc.subjectabsolute configurationen-US
dc.subjectditerpenoiden-US
dc.subjectX-ray diffractionen-US
dc.subjectcrystal and supramolecular structureen-US
dc.titleABSOLUTE CONFIGURATION OF MULINOLIC ACIDen-US
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion


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