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dc.contributor.authorLópez Francés, Adrián
dc.contributor.authorDel Corte Solaguren-Beascoa, Xabier
dc.contributor.authorMartínez de Marigorta Izaga, Edorta ORCID
dc.contributor.authorPalacios Gambra, Francisco Javier ORCID
dc.contributor.authorVicario Hernando, Javier ORCID
dc.date.accessioned2021-04-14T10:01:09Z
dc.date.available2021-04-14T10:01:09Z
dc.date.issued2021-03-16
dc.identifier.citationMolecules 26(6) : (2021) // Article ID 1654es_ES
dc.identifier.issn1420-3049
dc.identifier.urihttp://hdl.handle.net/10810/50925
dc.description.abstractAn Ugi three-component reaction using preformed α-phosphorated N-tosyl ketimines with different isocyanides in the presence of a carboxylic acid affords tetrasubstituted α-aminophosphonates. Due to the high steric hindrance, the expected acylated amines undergo a spontaneous elimination of the acyl group. The reaction is applicable to α-aryl ketimines bearing a number of substituents and several isocyanides. In addition, the densely substituted α-aminophosphonate substrates showed in vitro cytotoxicity, inhibiting the growth of carcinoma human tumor cell line A549 (carcinomic human alveolar basal epithelial cell).es_ES
dc.description.sponsorshipFinancial support by Ministerio de Economía, Industria y Competividad (MINECO, CTQ-2015-67871R) and Gobierno Vasco (GV, IT 992-16) is gratefully acknowledged. X.d.C. and A.L.-F. thank the Basque Country Government for a predoctoral grant.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/CTQ-2015-67871Res_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjectmulticomponent synthesises_ES
dc.subjectUgi reactiones_ES
dc.subjectα-aminophosphonateses_ES
dc.subjecttetrasubstituted carbonses_ES
dc.subjectantiproliferative effectes_ES
dc.titleUgi Reaction on α-Phosphorated Ketimines for the Synthesis of Tetrasubstituted α-Aminophosphonates and Their Applications as Antiproliferative Agentses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2021-03-26T14:09:33Z
dc.rights.holder2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/1420-3049/26/6/1654/htmes_ES
dc.identifier.doi10.3390/molecules26061654
dc.departamentoesQuímica orgánica I
dc.departamentoeuKimika organikoa I


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2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).