Reaction of acyclic enaminones with methoxymethylene meldrum's acid: synthetic and structural implications



Document title: Reaction of acyclic enaminones with methoxymethylene meldrum's acid: synthetic and structural implications
Journal: Journal of the Brazilian Chemical Society
Database: PERIÓDICA
System number: 000311240
ISSN: 0103-5053
Authors: 1

2

Institutions: 1Universidade Federal de Goias, Instituto de Quimica, Goiania, Goias. Brasil
2Universidade Federal de Goias, Instituto de Fisica, Goiania, Goias. Brasil
Year:
Season: Ene
Volumen: 14
Number: 1
Pages: 107-112
Country: Brasil
Language: Inglés
Document type: Artículo
Approach: Experimental
English 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
Portuguese abstract A reação de enaminonas com o derivado metoximetilênico do ácido de Meldrum forneceu N-adutos e/ou C-adutos das enaminonas, em rendimentos moderados a bons. A regioquímica da reação se revelou dependente do substituinte do nitrogênio da enaminona, e o C-aduto formado é precursor para 2-piridonas. A análise da difração de raios X de dois N-adutos revelou que estes adutos possuem a configuração Z-s-Z
Disciplines: Química
Keyword: Química orgánica,
Enaminonas,
Acido de Meldrum,
2-piridona,
Reacciones de aza-anulación
Keyword: Chemistry,
Organic chemistry,
Enaminones,
Meldrum's acid,
2-pyridone,
Aza-annulation reactions
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