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dc.date.accessioned 2023-02-15T19:06:21Z
dc.date.available 2023-02-15T19:06:21Z
dc.date.issued 2016
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/148964
dc.description.abstract Background: Dihydrofurocoumarins are a large family of compounds, among them, dihydroangelicins and dihydropsoralens, are present in various plant species with varied biological activity. Several strategies have been developed for synthesizing these compounds and various catalysts have been used for this purpose. Methods: In this work, we report the synthesis of 8,9-dihydrofuran [2, 3-h] coumarins using allyloxycoumarin cycloaddition in sustainable conditions: absence of solvents, application of microwave radiation, and insoluble acid catalysis by means of heteropolyacids with Preyssler structure, [H14(NaP5MoW29O110)]. Conclusion: With these conditions, and testing sustainability by means of Eco-Scale and E-factor, we replace the use of solvents and mineral acids having a great impact on the environment with a solid, easily recoverable heteropolyacid. en
dc.format.extent 242 - 247 es
dc.language en es
dc.subject Dihydroangelicins es
dc.subject Dihydrofuocoumarins es
dc.subject Microwave radiation es
dc.subject Green chemistry es
dc.subject Heteopolyacid es
dc.subject Preyysler structure es
dc.title A Solvent-free Method for Synthesis of Dihydroangelicins using Microwaves en
dc.type Articulo es
sedici.identifier.other https://doi.org/10.2174/2213346104666170224101037 es
sedici.identifier.issn 2213-3461 es
sedici.identifier.issn 2213-347X es
sedici.creator.person Ruiz, Diego Manuel es
sedici.creator.person Autino, Juan Carlos es
sedici.creator.person Romanelli, Gustavo Pablo es
sedici.subject.materias Química es
sedici.description.fulltext true es
mods.originInfo.place Centro de Investigación en Sanidad Vegetal es
mods.originInfo.place Centro de Investigación y Desarrollo en Ciencias Aplicadas es
sedici.subtype Preprint 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 Green Chemistry es
sedici.relation.journalVolumeAndIssue vol. 3, no. 3 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)