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dc.date.accessioned 2019-10-10T13:55:44Z
dc.date.available 2019-10-10T13:55:44Z
dc.date.issued 2008
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/83026
dc.description.abstract In this work, we report the use of bulk and silica-supported Wells-Dawson acid (H2P2W18O62.24H2O) as reusable, heterogeneous catalysts to obtain substituted flavones and chromones for the cyclization of 1-(2-hydroxyphenyl)-3-aryl-1,3-propanediones. The reaction experiments were performed using toluene as solvent at reflux and in the absence of solvent, at 110°C. Under these conditions eleven examples were obtained with very good yields (82-91%) and high selectivity. The catalysts were easily recycled and reused without loss of their catalytic activity. The presented synthetic method is a simple, clean and environmentally friendly alternative for synthesizing substituted flavones and chromones. en
dc.format.extent 123-130 es
dc.language en es
dc.subject Acid catalysis es
dc.subject Chromones es
dc.subject Flavones es
dc.subject H2P2W18O62.24H2O es
dc.subject Silica gel-supported catalyst es
dc.title Synthesis of substituted flavones and chromones using a Wells-Dawson heteropolyacid as catalyst en
dc.type Articulo es
sedici.identifier.other doi:10.3998/ark.5550190.0009.b12 es
sedici.identifier.other eid:2-s2.0-46249102401 es
sedici.identifier.issn 1551--701 es
sedici.creator.person Bennardi, Daniel Oscar es
sedici.creator.person Romanelli, Gustavo Pablo es
sedici.creator.person Jios, Jorge Luis es
sedici.creator.person Autino, Juan Carlos es
sedici.creator.person Baronetti, Graciela Teresita es
sedici.creator.person Thomas, Horacio Jorge es
sedici.subject.materias Química es
sedici.description.fulltext true es
mods.originInfo.place Centro de Investigación y Desarrollo en Ciencias Aplicadas es
mods.originInfo.place Facultad de Ciencias Agrarias y Forestales es
mods.originInfo.place Laboratorio de Servicios a la Industria y al Sistema Científico es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0)
sedici.rights.uri http://creativecommons.org/licenses/by-nc/3.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle Arkivoc es
sedici.relation.journalVolumeAndIssue vol. 2008, no. 11 es


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Creative Commons Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0)