Access to 3-aroylchromanones from dibenzoylmethanes via an iron-catalyzed α-methylenation reaction.

dc.contributor.authorGouveia, Ana Paula Araújo
dc.contributor.authorTaylor, Jason Guy
dc.date.accessioned2019-05-06T16:47:58Z
dc.date.available2019-05-06T16:47:58Z
dc.date.issued2018
dc.description.abstractA simple and straightforward synthesis of 3‐aroylchromanones based on a tandem iron catalyzed α‐methylenation – intramolecular oxy‐Michael addition reaction of dibenzoylmethanes with N,N‐dimethylacetamide is described. The reaction employs FeCl3 as catalyst under aerobic conditions to afford the corresponding 3‐aroylchromanones and tolerates a variety of substituents on both aromatic rings.pt_BR
dc.identifier.citationGOUVEIA, A. P. A.; TAYLOR, J. G. Access to 3-aroylchromanones from dibenzoylmethanes via an iron-catalyzed α-methylenation reaction. ChemistrySelect, v. 3, n. 4, p. 3965-3969, abr. 2018. Disponível em: <https://onlinelibrary.wiley.com/doi/full/10.1002/slct.201800029>. Acesso em: 7 mar. 2019.pt_BR
dc.identifier.doihttps://doi.org/10.1002/slct.201800029pt_BR
dc.identifier.issn2365-6549
dc.identifier.urihttp://www.repositorio.ufop.br/handle/123456789/11202
dc.identifier.uri2https://onlinelibrary.wiley.com/doi/full/10.1002/slct.201800029pt_BR
dc.language.isoen_USpt_BR
dc.rightsrestritopt_BR
dc.subjectChromanonespt_BR
dc.subjectN,N-dimethylacetamide homoisoflavonoidspt_BR
dc.titleAccess to 3-aroylchromanones from dibenzoylmethanes via an iron-catalyzed α-methylenation reaction.pt_BR
dc.typeArtigo publicado em periodicopt_BR
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