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

dc.contributor.author	Araújo, Flavia Magalhães
dc.contributor.author	Ventura, Wellington Martins
dc.contributor.author	Taylor, Jason Guy
dc.date.accessioned	2017-06-01T15:29:51Z
dc.date.available	2017-06-01T15:29:51Z
dc.date.issued	2014
dc.description.abstract	A 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.	pt_BR
dc.identifier.citation	ARAÚJO, F. M.; VENTURA, W. M.; TAYLOR, J. G. Synthesis of a benzannulated pyrrolizidine by a copper-catalyzed intramolecular a-arylation reaction. Helvetica Chimica Acta, v. 97, p. 569-573, 2014. Disponível em: <http://onlinelibrary.wiley.com/doi/10.1002/hlca.201300313/abstract>. Acesso em: 20 abr. 2017.	pt_BR
dc.identifier.doi	https://doi.org/10.1002/hlca.201300313
dc.identifier.issn	1522-2675
dc.identifier.uri	http://www.repositorio.ufop.br/handle/123456789/7846
dc.identifier.uri2	http://onlinelibrary.wiley.com/doi/10.1002/hlca.201300313/abstract	pt_BR
dc.language.iso	en_US	pt_BR
dc.rights	restrito	pt_BR
dc.title	Synthesis of a benzannulated pyrrolizidine by a copper-catalyzed intramolecular a-arylation reaction.	pt_BR
dc.type	Artigo publicado em periodico	pt_BR

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