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dc.contributor.authorReyes Martín, Efraim
dc.contributor.authorPrieto Aretxabaleta, Liher ORCID
dc.contributor.authorCarrillo Fernández, María Luisa ORCID
dc.contributor.authorUria Pujana, Uxue ORCID
dc.contributor.authorVicario Hernando, José Luis ORCID
dc.date.accessioned2023-12-14T10:12:53Z
dc.date.available2023-12-14T10:12:53Z
dc.date.issued2022-07-21
dc.identifier.citationSynthesis 54(19) : 4167-4183(2022)es_ES
dc.identifier.issn0039-7881
dc.identifier.issn1437-210X
dc.identifier.urihttp://hdl.handle.net/10810/63374
dc.description.abstractTransannular reactions have shown a remarkable performance for the construction of polycyclic scaffolds from medium- or large-sized cyclic molecules in an unconventional manner. Recent examples of transannular reactions reported from 2011 have been reviewed, emphasizing the excellent performance of this approach when accessing the target compounds. This review also highlights how this methodology provides an alternative approach to other commonly used strategies for the construction of cyclic entities such as cyclization or cycloaddition reactions.es_ES
dc.description.sponsorshipMCIU (FEDER-PID2020-118422-gb-100), Basque Government (IT908-16)es_ES
dc.language.isoenges_ES
dc.publisherThiemees_ES
dc.relationinfo:eu-repo/grantAgreement/MCIU/FEDER-PID2020-118422-gb-100es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjecttransannular reactiones_ES
dc.subjectbicyclic compoundses_ES
dc.subjectcyclizationes_ES
dc.subjectfused-ring systemses_ES
dc.subjectheterocycleses_ES
dc.subjectmacrocycleses_ES
dc.subjectnatural productses_ES
dc.subjecttotal synthesises_ES
dc.titleRecent Developments in Transannular Reactionses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2022. Thieme. All rights reservedes_ES
dc.relation.publisherversionhttps://doi.org/10.1055/a-1843-1954es_ES
dc.identifier.doi10.1055/a-1843-1954
dc.departamentoesQuímica Orgánica e Inorgánicaes_ES
dc.departamentoeuKimika Organikoa eta Ez-Organikoaes_ES


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