dc.creatorAstudillo, Luis
dc.creatorDe La Guarda, Waleska
dc.creatorGutiérrez, Margarita
dc.creatorSan Martín Barrientos, Aurelio
dc.date.accessioned2018-12-20T14:08:19Z
dc.date.available2018-12-20T14:08:19Z
dc.date.created2018-12-20T14:08:19Z
dc.date.issued2009
dc.identifierZeitschrift fur Naturforschung - Section C Journal of Biosciences, Volumen 64, Issue 3-4, 2018, Pages 215-218
dc.identifier09395075
dc.identifier10.1515/znc-2009-3-411
dc.identifierhttps://repositorio.uchile.cl/handle/2250/154179
dc.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.
dc.languageen
dc.publisherVerlag der Zeitschrift fur Naturforschung
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceZeitschrift fur Naturforschung - Section C Journal of Biosciences
dc.subjectBiotransformation
dc.subjectImino Diels-Alder Reaction
dc.subjectMortierella isabelina
dc.subjectTetrahydroquinoline
dc.titleSynthesis and biotransformation of tetrahydroquinoline by Mortierella isabelina
dc.typeArtículos de revistas


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