On the Mechanism of Rhodium-Catalyzed [6+2] Cycloaddition of 2-Vinylcylobutanones and Alknenes

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Físicagl
dc.contributor.authorMontero Campillo, María de la Merced
dc.contributor.authorCabaleiro Lago, Enrique Manuel
dc.contributor.authorRodríguez Otero, Jesús
dc.date.accessioned2021-08-18T08:38:57Z
dc.date.available2021-08-18T08:38:57Z
dc.date.issued2007
dc.descriptionThe 11th International Electronic Conference on Synthetic Organic Chemistry session Computational Chemistrygl
dc.description.abstractThe intramolecular [6+2] cycloaddition mechanism of 2­vinylcyclobutanones and alkenes catalyzed by the [Rh(CO)2Cl]2 dimer has been studied using density functional theory, comparing this multistep process with the one­step reaction in absence of catalyst. This possible mechanism agrees with what was previously experimentally suggested. Calculations have also allowed to explain the selectivity of the reactiongl
dc.identifier.citationMontero­ Campillo, M.M.; Cabaleiro ­Lago, E.M.; Rodríguez ­Otero, J. On the Mechanism of Rhodium-Catalyzed [6+2] Cycloaddition of 2-Vinylcylobutanones and Alknenes, in Proceedings of the 11th International Electronic Conference on Synthetic Organic Chemistry, 1–30 November 2007, MDPI: Basel, Switzerland, doi:10.3390/ecsoc-11-01369gl
dc.identifier.doi10.3390/ecsoc-11-01369
dc.identifier.isbn3-906980-19-7
dc.identifier.urihttp://hdl.handle.net/10347/26833
dc.language.isoenggl
dc.publisherMDPIgl
dc.relation.ispartofseriesElectronic Conference on Synthetic Organic Chemistry;11
dc.relation.publisherversionhttps://doi.org/10.3390/ecsoc-11-01369gl
dc.rights© 2007 The author(s). Published by MDPI, Basel, Switzerland. Open Accessgl
dc.rights.accessRightsopen accessgl
dc.titleOn the Mechanism of Rhodium-Catalyzed [6+2] Cycloaddition of 2-Vinylcylobutanones and Alknenesgl
dc.typebook partgl
dspace.entity.typePublication
relation.isAuthorOfPublicationcae389b7-4a38-481e-b348-4a3d4d6707fb
relation.isAuthorOfPublication41c7b009-96a5-4225-97dc-0feda160d770
relation.isAuthorOfPublication.latestForDiscoverycae389b7-4a38-481e-b348-4a3d4d6707fb

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