Artículo

Novel Cyclic Enaminone Esters and N-Heterocycles by Divergent Chemical Behavior through Amine-Mediated Reactions

Luna, Liliana Edith; Tontarelli, Walter; Forastieri, Pamela SoledadIcon ; Cravero, Raquel MariaIcon
Fecha de publicación: 07/2015
Editorial: Wiley VCH Verlag
Revista: Helvetica Chimica Acta
ISSN: 0018-019X
Idioma: Inglés
Tipo de recurso: Artículo publicado
Clasificación temática:

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.
Palabras clave: Acridines, Decahydrodioxo- , Cycloadditions , Enaminones , Intramolecular H-Bonding , Michael-Michael Reaction , Microwave-Assisted Reactions
 
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info:eu-repo/semantics/openAccess Excepto donde se diga explícitamente, este item se publica bajo la siguiente descripción: Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Unported (CC BY-NC-SA 2.5)
Identificadores
URI: http://hdl.handle.net/11336/37926
DOI: http://dx.doi.org/10.1002/hlca.201400376
URL: http://onlinelibrary.wiley.com/doi/10.1002/hlca.201400376/abstract
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Articulos(IQUIR)
Articulos de INST.DE QUIMICA ROSARIO
Citación
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
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