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Studies on the preparation of aminobipyridines and bipyridine sultams via an intramolecular free radical pathway

dc.contributor.authorRecio, Javier
dc.contributor.authorFilace, Fabiana
dc.contributor.authorGala, Elena
dc.contributor.authorPérez-Redondo, Adrián
dc.contributor.authorÁlvarez-Builla, Julio
dc.contributor.authorBurgos, Carolina
dc.date.accessioned2024-02-01T14:17:57Z
dc.date.available2024-02-01T14:17:57Z
dc.date.issued2020-03-04
dc.identifier.citationRSC Advances, 2020, 10, 10447es
dc.identifier.urihttps://hdl.handle.net/10115/29431
dc.description.abstractA variety of aminated bipyridines and bipyridine sultams are prepared by intramolecular radical [1,5]-ipso and [1,6]-ortho substitutions, using a sulfonamide as a linker to connect the pyridyl radical to the pyridine under attack. For the cases studied, different regiochemistries are observed depending on the initial position of the sulfonamide linker.es
dc.language.isoenges
dc.publisherROYAL SOC CHEMISTRYes
dc.rightsAtribución-NoComercial 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.subjectIpso-substitutiones
dc.subjectBiarylsderivativeses
dc.subjectCyclizationes
dc.subjectC-H Arylationes
dc.titleStudies on the preparation of aminobipyridines and bipyridine sultams via an intramolecular free radical pathwayes
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1039/d0ra02026ees
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses


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