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Authordc.contributor.authorAstudillo, Luis 
Authordc.contributor.authorDe La Guarda, Waleska 
Authordc.contributor.authorGutiérrez, Margarita 
Authordc.contributor.authorSan Martín Barrientos, Aurelio 
Admission datedc.date.accessioned2018-12-20T14:08:19Z
Available datedc.date.available2018-12-20T14:08:19Z
Publication datedc.date.issued2009
Cita de ítemdc.identifier.citationZeitschrift fur Naturforschung - Section C Journal of Biosciences, Volumen 64, Issue 3-4, 2018, Pages 215-218
Identifierdc.identifier.issn09395075
Identifierdc.identifier.other10.1515/znc-2009-3-411
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/154179
Abstractdc.description.abstractTetrahydroquinoline (1), prepared by a traditional synthetic method, the imino Diels-Alder reaction, was biotransformed by Mortierella isabelina to afford a new compound, 2, characterized by spectroscopic methods. © 2009 Verlag der Zeitschrift für Naturforschung Tübingen.
Lenguagedc.language.isoen
Publisherdc.publisherVerlag der Zeitschrift fur Naturforschung
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceZeitschrift fur Naturforschung - Section C Journal of Biosciences
Keywordsdc.subjectBiotransformation
Keywordsdc.subjectImino Diels-Alder Reaction
Keywordsdc.subjectMortierella isabelina
Keywordsdc.subjectTetrahydroquinoline
Títulodc.titleSynthesis and biotransformation of tetrahydroquinoline by Mortierella isabelina
Document typedc.typeArtículo de revista
dcterms.accessRightsdcterms.accessRightsAcceso Abierto
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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