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dc.contributor.advisorGómez Bengoa, Enrique
dc.contributor.authorPérez Furundarena, Haritz
dc.contributor.otherF. CIENCIAS QUIMICAS
dc.contributor.otherKIMIKA ZIENTZIEN F.
dc.date.accessioned2020-10-16T16:12:59Z
dc.date.available2020-10-16T16:12:59Z
dc.date.issued2020-10-16
dc.identifier.urihttp://hdl.handle.net/10810/46958
dc.description.abstract[EU]Lan honetan laborategian egin diren diamina kiralez organokatalizatutako enamina eta maleimida molekulen arteko Michael adizio erreakzioaren enantioselektibotasuna ikerketa konputazionalen bidez azaldu da. Azterketan katalizatazaileak erreakzioan duen mekanismoan sakondu da, diamina organokatalizatzailearen talde desberdinen eta disolbatzailearen efektua azalduz purutasun enantiomerikoan.es_ES
dc.description.abstract[EN]In this work, Michael addition of enamine and maleimide organocatalyzed by diamine reactions have been explained by a computational study. In the research, the mechanism of the catalyst has been studied in depth, explaining the effect of different groups of the diamine organocatalyst and the solvent.es_ES
dc.language.isoeuses_ES
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleDiamina kiralak organokatalisian: Maleimidaren Michael erreakzioaren ikerketa konputazionalaes_ES
dc.typeinfo:eu-repo/semantics/bachelorThesis
dc.date.updated2018-10-02T14:12:54Z
dc.language.rfc3066es
dc.rights.holder© 2019, el autor
dc.contributor.degreeGrado en Química;;Kimikako Graduaes_ES
dc.identifier.gaurassign80296-766113


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