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

dc.contributor.author	Recio, Javier
dc.contributor.author	Filace, Fabiana
dc.contributor.author	Gala, Elena
dc.contributor.author	Pérez-Redondo, Adrián
dc.contributor.author	Álvarez-Builla, Julio
dc.contributor.author	Burgos, Carolina
dc.date.accessioned	2024-02-01T14:17:57Z
dc.date.available	2024-02-01T14:17:57Z
dc.date.issued	2020-03-04
dc.description.abstract	A 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.identifier.citation	RSC Advances, 2020, 10, 10447	es
dc.identifier.doi	10.1039/d0ra02026e	es
dc.identifier.uri	https://hdl.handle.net/10115/29431
dc.language.iso	eng	es
dc.publisher	ROYAL SOC CHEMISTRY	es
dc.rights	Atribución-NoComercial 4.0 Internacional	*
dc.rights.accessRights	info:eu-repo/semantics/openAccess	es
dc.rights.uri	http://creativecommons.org/licenses/by-nc/4.0/	*
dc.subject	Ipso-substitution	es
dc.subject	Biarylsderivatives	es
dc.subject	Cyclization	es
dc.subject	C-H Arylation	es
dc.title	Studies on the preparation of aminobipyridines and bipyridine sultams via an intramolecular free radical pathway	es
dc.type	info:eu-repo/semantics/article	es

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