Please use this identifier to cite or link to this item: https://repositorio.ufba.br/handle/ri/14379
metadata.dc.type: Artigo de Periódico
Title: Reaction of acyclic enaminones with methoxymethylene meldrum's acid. Synthetic and structural implications
Other Titles: Journal of the Brazilian Chemical Society
Authors: Cunha, Silvio do Desterro
Silva, Viviane C. da
Napolitano, Hamilton B.
Lariucci, Carlito
Vencato, Ivo
metadata.dc.creator: Cunha, Silvio do Desterro
Silva, Viviane C. da
Napolitano, Hamilton B.
Lariucci, Carlito
Vencato, Ivo
Abstract: The reaction of acyclic enaminones with methoxymethylene Meldrum's acid afforded N-adduct and/or C-adduct of enaminones in moderate to good yields. The regiochemistry of this reaction depends on the N-amino substituent of the enaminone. The C-adduct is a precursor to 2-pyridones. X-ray analysis of two N-adducts were investigated and the Z-s-Z configuration assigned.
Keywords: Enaminones
Meldrum's acid
Aza-annulation
2-pyridone
metadata.dc.publisher.country: Brasil
metadata.dc.rights: Acesso Aberto
URI: http://repositorio.ufba.br/ri/handle/ri/14379
Issue Date: 2003
Appears in Collections:Artigo Publicado em Periódico (Química)

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