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Publicação:
One-Step Synthesis of Methoxylated Phloroglucinol Derivatives Promoted by Niobium Pentachloride: An Experimental and Theoretical Approach

dc.contributor.authorDos Santos, Willian Henrique [UNESP]
dc.contributor.authorDe Oliveira, Eliezer Fernando [UNESP]
dc.contributor.authorLavarda, Francisco Carlos [UNESP]
dc.contributor.authorLeonarczyk, Ives Antonio
dc.contributor.authorFerreira, Marco Antonio Barbosa
dc.contributor.authorDa Silva-Filho, Luiz Carlos [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.date.accessioned2018-12-11T17:31:34Z
dc.date.available2018-12-11T17:31:34Z
dc.date.issued2017-06-01
dc.description.abstractPhloroglucinol derivatives are an important class of natural compounds featuring the rhodomyrtone derivatives. In this work, the synthesis of compounds with a structure core of rhodomyrtosone I is described using a multicomponent reaction between aldehyde derivatives, dihydroresorcinol, and 3,5-dimethoxyphenol promoted by niobium pentachloride. This new method is simple, cost-effective, and provides a good yield. In addition, it can be conducted in good reaction times. Using Density Functional Theory (DFT) studies, bases are provided for a proposed reaction mechanism for the multicomponent reaction by exploring the energetics of proposed reactive intermediates and transition states.en
dc.description.affiliationDepartment of Chemistry Faculty of Sciences São Paulo State University (UNESP)
dc.description.affiliationDepartment of Physics Faculty of Sciences São Paulo State University (UNESP)
dc.description.affiliationDepartment of Chemistry Federal University of São Carlos (UFSCar), Rodovia Washington Luís, km 235 - SP-310
dc.description.affiliationUnespDepartment of Chemistry Faculty of Sciences São Paulo State University (UNESP)
dc.description.affiliationUnespDepartment of Physics Faculty of Sciences São Paulo State University (UNESP)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2012/21983-0
dc.description.sponsorshipIdFAPESP: 2014/20410-1
dc.description.sponsorshipIdFAPESP: 2015/08541-6
dc.description.sponsorshipIdFAPESP: 2016/01599-1
dc.format.extent2402-2410
dc.identifierhttp://dx.doi.org/10.1055/s-0036-1588730
dc.identifier.citationSynthesis (Germany), v. 49, n. 11, p. 2402-2410, 2017.
dc.identifier.doi10.1055/s-0036-1588730
dc.identifier.issn1437-210X
dc.identifier.issn0039-7881
dc.identifier.scopus2-s2.0-85013668260
dc.identifier.urihttp://hdl.handle.net/11449/178664
dc.language.isoeng
dc.relation.ispartofSynthesis (Germany)
dc.relation.ispartofsjr0,974
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectDFT studies
dc.subjectLewis acid
dc.subjectmulticomponent reactions
dc.subjectniobium pentachloride
dc.subjectphloroglucinol derivatives
dc.titleOne-Step Synthesis of Methoxylated Phloroglucinol Derivatives Promoted by Niobium Pentachloride: An Experimental and Theoretical Approachen
dc.typeArtigo
dspace.entity.typePublication
unesp.departmentFísica - FCpt

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