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

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MetadadosDescriçãoIdioma
Autor(es): dc.creatorGouveia, Ana Paula Araújo-
Autor(es): dc.creatorTaylor, Jason Guy-
Data de aceite: dc.date.accessioned2025-08-21T15:35:05Z-
Data de disponibilização: dc.date.available2025-08-21T15:35:05Z-
Data de envio: dc.date.issued2019-05-06-
Data de envio: dc.date.issued2019-05-06-
Data de envio: dc.date.issued2018-
Fonte completa do material: dc.identifierhttp://www.repositorio.ufop.br/handle/123456789/11202-
Fonte completa do material: dc.identifierhttps://onlinelibrary.wiley.com/doi/full/10.1002/slct.201800029-
Fonte completa do material: dc.identifierhttps://doi.org/10.1002/slct.201800029-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/capes/1018971-
Descrição: dc.descriptionA 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.-
Formato: dc.formatapplication/pdf-
Idioma: dc.languageen-
Direitos: dc.rightsrestrito-
Palavras-chave: dc.subjectChromanones-
Palavras-chave: dc.subjectN,N-dimethylacetamide homoisoflavonoids-
Título: dc.titleAccess to 3-aroylchromanones from dibenzoylmethanes via an iron-catalyzed α-methylenation reaction.-
Aparece nas coleções:Repositório Institucional - UFOP

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