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SYNTHESIS OF 6-TERT-OCTYL AND 6,8-DITERT-BUTYL COUMARINS, TWO COUMARINS OF BIOLOGICAL INTEREST

dc.creatorZárraga Olavarría, Miguel
dc.creatorDahrouch, Mohamed
dc.creatorLisboa, Esteban
dc.creatorArroyo, Patricia
dc.creatorMiranda, Alberto
dc.date2021-06-13
dc.date.accessioned2021-07-15T14:52:05Z
dc.date.available2021-07-15T14:52:05Z
dc.identifierhttp://www.jcchems.com/index.php/JCCHEMS/article/view/1740
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/169999
dc.descriptionIn this study, the synthesis of new coumarins with aliphatic chains is discussed. The incorporation of the 6-tert-octyl and 6,8-ditert-butyl chains into a coumarin structure from alkylphenols, allows obtaining hydrophobic coumarins with good yields. These coumarins can be potential modulators of TRPV1 receptors. Synthesis and spectroscopic data of these new coumarins are analyzed.  en-US
dc.formatapplication/pdf
dc.formatapplication/pdf
dc.languageeng
dc.publisherSociedad Chilena de Químicaen-US
dc.relationhttp://www.jcchems.com/index.php/JCCHEMS/article/view/1740/478
dc.relationhttp://www.jcchems.com/index.php/JCCHEMS/article/view/1740/479
dc.rightsCopyright (c) 2021 SChQen-US
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/4.0en-US
dc.sourceJournal of the Chilean Chemical Society; Vol 66 No 2 (2021): Journal of the Chilean Chemical Society; 5220-5222en-US
dc.source0717-9707
dc.source0717-9324
dc.subjectCOUMARINSen-US
dc.subjecthydrophobicen-US
dc.subjectTRPV1en-US
dc.titleSYNTHESIS OF 6-TERT-OCTYL AND 6,8-DITERT-BUTYL COUMARINS, TWO COUMARINS OF BIOLOGICAL INTERESTen-US
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion


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