Synthesis of a benzannulated pyrrolizidine by a copper-catalyzed intramolecular a-arylation reaction.

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MetadadosDescriçãoIdioma
Autor(es): dc.creatorAraújo, Flavia Magalhães-
Autor(es): dc.creatorVentura, Wellington Martins-
Autor(es): dc.creatorTaylor, Jason Guy-
Data de aceite: dc.date.accessioned2025-08-21T15:27:44Z-
Data de disponibilização: dc.date.available2025-08-21T15:27:44Z-
Data de envio: dc.date.issued2017-06-01-
Data de envio: dc.date.issued2017-06-01-
Data de envio: dc.date.issued2014-
Fonte completa do material: dc.identifierhttp://www.repositorio.ufop.br/handle/123456789/7846-
Fonte completa do material: dc.identifierhttp://onlinelibrary.wiley.com/doi/10.1002/hlca.201300313/abstract-
Fonte completa do material: dc.identifierhttps://doi.org/10.1002/hlca.201300313-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/capes/1015622-
Descrição: dc.descriptionA synthetic route to the pyrrolo[1,2-a]indole ring system (benzannulated pyrrolizidine) involving a base-induced intramolecular aza-Michael reaction as the key C N bond-forming penultimate step, followed by a Cu-catalyzed intramolecular a-arylation reaction, to provide the tricyclic framework over six steps is described.-
Formato: dc.formatapplication/pdf-
Idioma: dc.languageen-
Direitos: dc.rightsrestrito-
Título: dc.titleSynthesis of a benzannulated pyrrolizidine by a copper-catalyzed intramolecular a-arylation reaction.-
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