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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.authorSoto Delgado, Jorge es_CL
Authordc.contributor.authorContreras Ramos, Renato es_CL
Admission datedc.date.accessioned2012-06-04T19:43:33Z
Available datedc.date.available2012-06-04T19:43:33Z
Publication datedc.date.issued2009-08-19
Cita de ítemdc.identifier.citationPhytochemistry, vol. 70, p. 1315–1320, 2009.es_CL
Identifierdc.identifier.issn0031-9422
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/119440
Abstractdc.description.abstractMeroditerpenoids, 2-[20(E)-30,70,110,150-tetramethylhexadec-2-en-10-yl]-6-methyl-1,4-benzohydroquinone diacetate and 40-chlorostypotriol triacetate, along with eight known compounds isolated from the dichloromethane extract of the brown alga Stypopodium flabelliforme after peracetylation are reported. One of them, 2-(1-oxo-hexadecyl)-1,3,5-trihydroxybenzene, is described for the first time within this genus. Structural elucidation was carried out on the basis of spectroscopic data and theoretical studies using GIAO/DFT analysis at B3LYP/6-31G(d) and mPW1PW91/6-31G(d) levels of theory for 40- chlorostypotriol. This isomer is the first metabolite from the Stypopodium genus possessing one halogen atom.es_CL
Patrocinadordc.description.sponsorshipThis investigation was subsidised by ‘‘Proyecto Anillo ACT-38” and FONDECYT Grant No. 1070715. JSD acknowledges MECESUP fellowship No. 0408.es_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherElsevieres_CL
Keywordsdc.subjectStypopodium flabelliformees_CL
Títulodc.titleAn unusual halogenated meroditerpenoid from Stypopodium flabelliforme: Studies by NMR spectroscopic and computational methodses_CL
Document typedc.typeArtículo de revista


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