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dc.contributor.authorPertejo, Pablo
dc.contributor.authorSancho-Medina, Andrea
dc.contributor.authorHermosilla, Tomás
dc.contributor.authorGonzález-Saiz, Beatriz
dc.contributor.authorGómez-Ayuso, Javier
dc.contributor.authorQuesada, Roberto
dc.contributor.authorMoreno, D. (1)
dc.contributor.authorCarreira-Barral, Israel
dc.contributor.authorGarcía-Valverde, María
dc.date2021
dc.date.accessioned2021-07-09T10:31:49Z
dc.date.available2021-07-09T10:31:49Z
dc.identifier.issn1420-3049
dc.identifier.urihttps://reunir.unir.net/handle/123456789/11585
dc.description.abstractThe use of arylglyoxal as starting material in Passerini and Ugi reactions affords β-ketoamides. This has allowed to study keto-enol tautomerism in these systems and assess the way in which the presence of acyloxy or aminoacyl groups bound to the C2 position affects such tautomerism, and to investigate the reactivity of both the enol and carbonyl forms. In this work we also prove the versatility of the Passerini reaction, since depending on the conditions to which the corresponding adducts are subjected different products of synthetic interest can be obtained.es_ES
dc.language.isoenges_ES
dc.publisherMoleculeses_ES
dc.relation.ispartofseries;vol. 26, nº 4
dc.relation.urihttps://www.mdpi.com/1420-3049/26/4/919es_ES
dc.rightsopenAccesses_ES
dc.subjectketo-enol tautomerismes_ES
dc.subjectpasserini adductes_ES
dc.subjectugi adductes_ES
dc.subjectlactonees_ES
dc.subjectlactamees_ES
dc.subject2-hydroxyglutaric acides_ES
dc.subjectScopuses_ES
dc.titleKeto-Enol Tautomerism in Passerini and Ugi Adductses_ES
dc.typeArticulo Revista Indexadaes_ES
reunir.tag~ARIes_ES
dc.identifier.doihttps://doi.org/10.3390/molecules26040919


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