Transition Metal Catalyzed Annulations Based On The Activation Of C-H Bonds

dc.contributor.advisorMascareñas Cid, José Luis
dc.contributor.advisorLópez García, Fernando
dc.contributor.advisorGulías Costa, Moisés
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Orgánicagl
dc.contributor.affiliationFacultade de Química
dc.contributor.authorFernández Fernández, David
dc.date.accessioned2019-09-24T08:03:16Z
dc.date.available2021-09-09T01:00:11Z
dc.date.issued2019
dc.description.abstractTransition metal catalysis is an impressive tool to promote relevant synthetic transformations. A particularly appealing chase are metal C–H activation protocols which are at the vanguard of organic synthesis due to the advantages in terms of atomic waste prevention, one of the principles of the Green Chemistry,10 step economy and selectivity. On the other hand, annulations processes are among the most appealing transformations in terms of atom economy, efficiency and increase in molecular complexity. Merging these processes result in a powerful strategy in the synthesis of challenging bioactive molecules.1 During this PhD work we have discovered several cyclization and cycloaddition transition-metal promoted reactions that allow to access to relevant cyclic scaffolds.gl
dc.identifier.urihttp://hdl.handle.net/10347/19804
dc.language.isoenggl
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectCatálise / Catalysisgl
dc.subjectAnelacións / Annulationsgl
dc.subjectActivación C-H / C-H Activationgl
dc.subjectMetais de transición / Transition Metalsgl
dc.subject.classificationMaterias::Investigación::23 Química::2306 Química orgánica::230611 Compuestos organometálicosgl
dc.subject.classificationMaterias::Investigación::23 Química::2306 Química orgánica::230618 Estructuras de las moléculas orgánicasgl
dc.titleTransition Metal Catalyzed Annulations Based On The Activation Of C-H Bondsgl
dc.typedoctoral thesisgl
dspace.entity.typePublication
relation.isAdvisorOfPublication5ae222c9-f626-432b-aac5-da78c06ed64f
relation.isAdvisorOfPublication47a6a088-27a9-412e-8422-0de4fd8af0d4
relation.isAdvisorOfPublication.latestForDiscovery5ae222c9-f626-432b-aac5-da78c06ed64f

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