Artículos de revistas
Novel Cyclic Enaminone Esters and N-Heterocycles by Divergent Chemical Behavior through Amine-Mediated Reactions
Fecha
2015-07Registro en:
Luna, Liliana Edith; Tontarelli, Walter; Forastieri, Pamela Soledad; Cravero, Raquel Maria; Novel Cyclic Enaminone Esters and N-Heterocycles by Divergent Chemical Behavior through Amine-Mediated Reactions; Wiley VCH Verlag; Helvetica Chimica Acta; 98; 7; 7-2015; 994-1003
0018-019X
CONICET Digital
CONICET
Autor
Luna, Liliana Edith
Tontarelli, Walter
Forastieri, Pamela Soledad
Cravero, Raquel Maria
Resumen
New acridinones and enaminone esters were synthesized by microwave-assisted tandem-Michael-Michael addition and cyclization from cyclohexane-1,3-diones. The reaction mechanism for both open and closed structures, and the presence of intramolecular twelve-membered rings derived from NH and OH H-bonds of enaminone esters are discussed.