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Intramolecular Addition of Heteroaryllithiums onto Activated Alkenes. Access to Heterofused Indolizines and Pyrroloazepines

dc.contributor.authorRebolledo Azcargorta, Ane
dc.contributor.authorCoya Díaz de Sarralde, Estibaliz
dc.contributor.authorPanaite, Ana María
dc.contributor.authorSotomayor Anduiza, María Nuria
dc.contributor.authorLete Expósito, María Esther
dc.date.accessioned2024-01-23T08:52:06Z
dc.date.available2024-01-23T08:52:06Z
dc.date.issued2017-02-23
dc.identifier.citationEuropean Journal of Organic Chemistry 2017 : 2462-2468 (2017)es_ES
dc.identifier.issn1099-0690
dc.identifier.urihttp://hdl.handle.net/10810/64228
dc.description.abstractHeteroaryllithiums, obtained via MesLi mediated halogen- lithium exchange, undergo intramolecular addition onto acrylamide and acrylate moieties. Both electron rich (thiophenyl) and electron deficient (pyridinyl, quinolinyl) heteroaromatic halides can be used for the formation of six- and seven membered rings, providing an efficient route to fused indolizines and pyrroloazepines in moderate to good yields.es_ES
dc.description.sponsorshipMinisterio de Economía y Competitividad (CTQ2013-41229-P, CTQ2016-74881-P), Gobierno Vasco (IT1045-16)es_ES
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/CTQ2013-41229-Pes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/CTQ2016-74881-Pes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectheteroaryllithiumes_ES
dc.subjectcarbolithiationes_ES
dc.subjectcyclizationes_ES
dc.subjectnitrogen heterocycleses_ES
dc.subjectcarbaniones_ES
dc.titleIntramolecular Addition of Heteroaryllithiums onto Activated Alkenes. Access to Heterofused Indolizines and Pyrroloazepineses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheimes_ES
dc.relation.publisherversionhttps://doi.org/10.1002/ejoc.201700123es_ES
dc.identifier.doi10.1002/ejoc.201700123
dc.departamentoesQuímica orgánica IIes_ES
dc.departamentoeuKimika organikoa IIes_ES


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