dc.contributor.advisor | Gómez Bengoa, Enrique | |
dc.contributor.author | Pérez Furundarena, Haritz | |
dc.contributor.other | F. CIENCIAS QUIMICAS | |
dc.contributor.other | KIMIKA ZIENTZIEN F. | |
dc.date.accessioned | 2020-10-16T16:12:59Z | |
dc.date.available | 2020-10-16T16:12:59Z | |
dc.date.issued | 2020-10-16 | |
dc.identifier.uri | http://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.iso | eus | es_ES |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.title | Diamina kiralak organokatalisian: Maleimidaren Michael erreakzioaren ikerketa konputazionala | es_ES |
dc.type | info:eu-repo/semantics/bachelorThesis | |
dc.date.updated | 2018-10-02T14:12:54Z | |
dc.language.rfc3066 | es | |
dc.rights.holder | © 2019, el autor | |
dc.contributor.degree | Grado en Química;;Kimikako Gradua | es_ES |
dc.identifier.gaurassign | 80296-766113 | |