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dc.date.accessioned 2024-03-08T18:26:08Z
dc.date.available 2024-03-08T18:26:08Z
dc.date.issued 2012
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/163622
dc.description.abstract We report the use of V, Bi and Bi-V Keggin structure where Mo is partially replaced by V, Bi, and Bi and V, respectively, in the solvent-free multicomponent synthesis of 3,4-dihydropyrimidin-2-(1H)-ones by the Biginelli method. The incorporation of V, Bi and Bi-V in the structure of PMo notably increases the catalytic activity. The following correlation between the yields of the 3,4-dihydropyrimidin-2-(1H)-ones and the number of acidic sites of the catalysts was observed: PMoBiV > PMoV > PMoBi > PMo. The re action experiments were performed in the absence of solvent, at 80ºC (1 h). Under these conditions and using the most active catalyst (PMoBiV), twelve examples were obtained with very good yields (80%–98%) and high selectivity. The catalyst was easily recycled and reused without appreciable loss of its catalytic activity. The synthetic method presented is a simple, clean and environmentally friendly alternative for the obtention of substituted 3,4-dihydropyrimidin-2-(1H)-ones. en
dc.language en es
dc.subject 3,4-Dihydropyrimidin-2-(1 H)-ones es
dc.subject Biginelli reaction es
dc.subject modified Keggin heteropolyacids es
dc.subject solvent-free synthesis es
dc.title Doped Keggin heteropolyacids as catalyst in the solvent-free, multicomponent synthesis of substituted 3,4-dihydropyrimidin-2(1 H)-ones en
dc.type Articulo es
sedici.creator.person D'Alessandro, Oriana es
sedici.creator.person Sathicq, Ángel Gabriel es
sedici.creator.person Sánchez, Laura Mabel es
sedici.creator.person Thomas, Horacio Jorge es
sedici.creator.person Vázquez, Patricia Graciela es
sedici.creator.person Constantieux, T. es
sedici.creator.person Romanelli, Gustavo Pablo es
sedici.subject.materias Ingeniería Química es
sedici.description.fulltext true es
mods.originInfo.place Centro de Investigación y Desarrollo en Tecnología de Pinturas es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by-nc-sa/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle Current Organic Chemistry es
sedici.relation.journalVolumeAndIssue vol. 16, no. 24 es


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Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)