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Authordc.contributor.authorAreche Medina, Carlos 
Authordc.contributor.authorSan Martín Barrientos, Aurelio es_CL
Authordc.contributor.authorRovirosa, Juana es_CL
Authordc.contributor.authorMuñoz, Marcelo A. es_CL
Authordc.contributor.authorHernández Barragán, Angelina es_CL
Authordc.contributor.authorBucio, María A. es_CL
Authordc.contributor.authorJoseph-Nathan, Pedro es_CL
Admission datedc.date.accessioned2010-07-13T14:20:16Z
Available datedc.date.available2010-07-13T14:20:16Z
Publication datedc.date.issued2010
Cita de ítemdc.identifier.citationJournal of Natural Products, 2010, Vol. 73, No. 1, 79–82en_US
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/119071
Abstractdc.description.abstractCareful examination of the published NMR data for isoepitaondiol, a meroditerpenoid from Stypopodium flabelliforme, suggests that its published structure 1 must be revised. On the basis of extensive 1D and 2D NMR studies, we now propose that structure 2, with a trans-anti-trans-anti-cis arrangement fits isoepitaondiol diacetate. The relative configuration of 2 was confirmed by single-crystal X-ray diffraction, while the absolute configuration was evidenced by vibrational circular dichroism in combination with DFT B3LYP/DGDZVP calculations.en_US
Patrocinadordc.description.sponsorshipFinancial support came from the Proyecto Anillo “ACT-38”, PBCT “PDA-13”, and CONACYT-Mexico Grant No. 61122.en_US
Lenguagedc.language.isoenen_US
Títulodc.titleStereostructure Reassignment and Absolute Configuration of Isoepitaondiol, a Meroditerpenoid from Stypopodium flabelliformeen_US
Document typedc.typeArtículo de revista


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