Palladium-Catalyzed [3+2+2] Cycloaddition Between Carbonyl-Tethered Alkylidenecyclopropanes and Isocyanates

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Orgánica
dc.contributor.authorRodiño Balboa, Ricardo
dc.contributor.authorMascareñas Cid, José Luis
dc.contributor.authorLópez García, Fernando José
dc.date.accessioned2025-07-11T10:59:49Z
dc.date.available2025-07-11T10:59:49Z
dc.date.issued2025-02-20
dc.description.abstractCarbonyl-tethered alkylidenecyclopropanes can react with aryl isocyanates in presence of Pd(0)-phosphoramidite catalysts to give seven-membered heterobicyclic products in a formal [3+2+2] cycloaddition process. The reaction involves the formation of a palladium π-allyl complex intermediate (A), which behaves as a formal 1,5-dipole, and can be trapped by externally added isocyanates. This report also includes preliminary assays of asymmetric variants, as well as DFT computational studies that shed some light on the nature of the catalytic cycle.
dc.description.peerreviewedSI
dc.description.sponsorshipThis work received financial support from Spanish grants (Grants PID2020-118579GB-I00, PID2022-137318OB-I00 and PID2023-152054NB-100, funded by MCIN/AEI, Grant IHRC22-00009 funded by MCIN/ISCIII and by the “European Union NextGenerationEU/PRTR”, the ORFEO-CINQA network RED2022-134287-T and a predoctoral fellowship to R. R.), the Consellería de Cultura, Educación e Ordenación Universitaria (Grant ED431C 2021/25 and Grant ED431G 2019/03: Centro Singular de Investigación de Galicia accreditation 2023–2027, ED431G 2023/03) and the European Union (European Regional Development Fund-ERDF).
dc.identifier.citationR. Rodiño, J. L. Mascareñas, F. López, Palladium-Catalyzed [3+2+2] Cycloaddition Between Carbonyl-Tethered Alkylidenecyclopropanes and Isocyanates. Helv. Chim. Acta 2025, 108, e202500011. https://doi.org/10.1002/hlca.202500011
dc.identifier.essn1522-2675
dc.identifier.issn0018-019X
dc.identifier.issn10.1002/hlca.202500011
dc.identifier.urihttps://hdl.handle.net/10347/42449
dc.journal.titleHelvetica Chimica Acta
dc.language.isoeng
dc.publisherWiley
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-118579GB-I00/ES/METODOS SINTETICOS ENANTIOSELECTIVOS BASADOS EN CATALISIS CON METALES DE TRANSICION Y APLICACIONES DE LOS MISMOS
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2022-137318OB-I00/ES/APLICACIONES BIOMEDICAS DE COMPLEJOS DE METALES DE TRANSICION: HERRAMIENTAS CATALITICAS Y DESARROLLO DE NUEVAS TERAPIAS ANTICANCER
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2023-152054NB-I00ES/METODOLOGIAS CATALITICAS ENANTIOSELECTIVAS PARA LA FORMACION DE ENLACES C-C Y C-N BASADAS EN METALES DE TRANSICION
dc.relation.projectIDinfo:eu-repo/grantAgreement/ISCIII/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/IHRC22%00009/Beyond metalloenzymes: Metal-grafted nanostructures for organometallic catalysis in live settings
dc.relation.publisherversionhttps://doi.org/10.1002/hlca.202500011
dc.rights© 2025 The Author(s). Helvetica Chimica Acta published by Wiley-VHCA AG. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
dc.rightsAttribution-NonCommercial 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectAlkylidenecyclopropane
dc.subjectPalladium
dc.subjectCycloaddition
dc.subjectDipole
dc.subjectZwitterionic
dc.subjectPhosphoramidite
dc.titlePalladium-Catalyzed [3+2+2] Cycloaddition Between Carbonyl-Tethered Alkylidenecyclopropanes and Isocyanates
dc.typejournal article
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isAuthorOfPublication5ae222c9-f626-432b-aac5-da78c06ed64f
relation.isAuthorOfPublication57da1b39-f2e1-4877-9965-de9833c59807
relation.isAuthorOfPublication.latestForDiscovery5ae222c9-f626-432b-aac5-da78c06ed64f

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