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

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

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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.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.rights.uri info:eu-repo/semantics/openAccess
dc.source 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.subject Química orgànica
dc.subject Reaccions químiques
dc.title Organocatalytic enantioselective functionalization of indoles in the carbocyclic ring with cyclic imines
dc.type info:eu-repo/semantics/article
dc.date.updated 2020-03-26T12:20:37Z
dc.identifier.doi https://doi.org/10.1039/C8NJ05577G
dc.identifier.idgrec 128978

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