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dc.contributor.authorSouii, Ichrak
dc.contributor.authorSanhoury, Med Abderrahmane
dc.contributor.authorVicario Hernando, Javier ORCID
dc.contributor.authorJiménez de Aberásturi González, Xabier
dc.contributor.authorEfrit, Mohamed L.
dc.contributor.authorM’rabet, Hedi
dc.contributor.authorDe los Santos Ruiz, Jesús Manuel ORCID
dc.date.accessioned2023-09-12T17:34:49Z
dc.date.available2023-09-12T17:34:49Z
dc.date.issued2023-06-09
dc.identifier.citationMolecules 28(12) : (2023) // Article ID 4678es_ES
dc.identifier.issn1420-3049
dc.identifier.urihttp://hdl.handle.net/10810/62455
dc.description.abstractSeveral bis(α-aminophosphonates) have been conveniently prepared in good yields using a straightforward multicomponent Kabachnik–Fields reaction between ethane 1,2-diamine or propane 1,3-diamine, diethylphosphite and aldehydes under catalyst-free conditions. The nucleophilic substitution reaction of bis(α-aminophosphonates) prepared and ethyl (2-bromomethyl)acrylate under mild reaction conditions afforded an original synthetic approach to a new series of bis(allylic-α-aminophosphonates).es_ES
dc.description.sponsorshipThe authors would like to thank the Ministry of Higher Education and Scientific research of Tunisia, the University of Tunis El Manar, the Ministerio de Ciencia, Innovación y Universidades (MCIU–Madrid) (PID2021-122558OB-I00, UE), and Gobierno Vasco (GV, IT1701-22; UPV-EHU) for their financial support. I.S. thanks the Ministry of Higher Education and Scientific research of Tunisia for a predoctoral grant.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MICINN/PID2021-122558OB-I00es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/es/
dc.subjectbis(α-aminophosphonates)es_ES
dc.subjectbis(allylic-α-aminophosphonates)es_ES
dc.subjectmulticomponent Kabachnik–Fields reactiones_ES
dc.subjectnucleophilic substitution reactiones_ES
dc.titleSynthesis and Characterization of a New Series of Bis(allylic-α-aminophosphonates) under Mild Reaction Conditionses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2023-06-27T13:22:12Z
dc.rights.holder© 2023 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 (https://creativecommons.org/licenses/by/ 4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/1420-3049/28/12/4678es_ES
dc.identifier.doi10.3390/molecules28124678
dc.departamentoesQuímica orgánica I
dc.departamentoeuKimika organikoa I


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© 2023 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 (https://creativecommons.org/licenses/by/ 4.0/).
Except where otherwise noted, this item's license is described as © 2023 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 (https://creativecommons.org/licenses/by/ 4.0/).