NAGIOS: RODERIC FUNCIONANDO

Organocatalytic enantioselective functionalization of indoles in the carbocyclic ring with cyclic imines

Repositori DSpace/Manakin

dc.contributor.author	Vila Descals, Carlos
dc.contributor.author	Tortosa, Arturo
dc.contributor.author	Blay Llinares, Gonzalo
dc.contributor.author	Muñoz, M. Carmen
dc.contributor.author	Pedro, José Ramón
dc.date.accessioned	2020-03-26T12:20:37Z
dc.date.available	2020-03-26T12:20:37Z
dc.date.issued	2019
dc.identifier.citation	Vila Descals, Carlos Tortosa, Arturo Blay Llinares, Gonzalo Muñoz, M. Carmen Pedro, José Ramón 2019 Organocatalytic enantioselective functionalization of indoles in the carbocyclic ring with cyclic imines New Journal of Chemistry 43 1 130 134
dc.identifier.uri	https://hdl.handle.net/10550/73672
dc.description.abstract	An organocatalytic enantioselective functionalization in the carbocyclic ring of indoles with benzoxathiazine 2,2-dioxides is described using a quinine-derived bifunctional organocatalyst. This aza-Friedel-Crafts reaction provides 4-indolyl, 5-indolyl and 7-indolyl sulfamidate derivatives in good yields (up to 99%) and with moderate to high enantioselectivities (up to 86% ee).
dc.language.iso	eng
dc.relation.ispartof	New Journal of Chemistry, 2019, vol. 43, num. 1, p. 130-134
dc.subject	Química orgànica
dc.subject	Reaccions químiques
dc.title	Organocatalytic enantioselective functionalization of indoles in the carbocyclic ring with cyclic imines
dc.type	journal article	es_ES
dc.date.updated	2020-03-26T12:20:37Z
dc.identifier.doi	10.1039/C8NJ05577G
dc.identifier.idgrec	128978
dc.rights.accessRights	open access	es_ES