Iridium-Catalyzed Hydrocarbonation of Unsaturated Systems: Enantioselective Synthesis of Heteropolycyclic Scaffolds

dc.contributor.advisorLópez García, Fernando José
dc.contributor.advisorMascareñas Cid, José Luis
dc.contributor.affiliationUniversidade de Santiago de Compostela. Escola de Doutoramento Internacional (EDIUS)
dc.contributor.authorArribas Domingo, Andrés
dc.date.accessioned2025-04-24T07:44:13Z
dc.date.available2025-04-24T07:44:13Z
dc.date.issued2025
dc.description.abstractThroughout the history of synthetic chemistry, the pursuit of more efficient and sustainable processes has become progressively significant. Modern organic synthesis not only seeks the preparation of target molecules but also designing processes that maximize resource efficiency. This involves conserving the maximum number of atoms from starting materials (atom economy), reducing the number of synthetic steps (step economy), and minimizing the need for intermediate purification (pot economy).
dc.description.programaUniversidade de Santiago de Compostela. Programa de Doutoramento en Ciencia e Tecnoloxía Química
dc.identifier.urihttps://hdl.handle.net/10347/41032
dc.language.isoeng
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectiridium
dc.subjectcatalysis
dc.subjecthydroarylation
dc.subjectC-H activation
dc.subjectenantioselective
dc.subject.classification230615 Mecanismos de reacción
dc.subject.classification230610 Compuestos heterocíclicos
dc.titleIridium-Catalyzed Hydrocarbonation of Unsaturated Systems: Enantioselective Synthesis of Heteropolycyclic Scaffolds
dc.typedoctoral thesis
dspace.entity.typePublication
relation.isAdvisorOfPublication57da1b39-f2e1-4877-9965-de9833c59807
relation.isAdvisorOfPublication5ae222c9-f626-432b-aac5-da78c06ed64f
relation.isAdvisorOfPublication.latestForDiscovery57da1b39-f2e1-4877-9965-de9833c59807

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
rep_3676.pdf
Size:
88.5 MB
Format:
Adobe Portable Document Format