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dc.contributor.authorGarcía Valverde, María 
dc.contributor.authorMarcaccini, Stefano .
dc.contributor.authorGonzález Ortega, Alfonso .
dc.contributor.authorRodríguez Vidal, Francisco Javier 
dc.contributor.authorRojo Cámara, Mª Josefa 
dc.contributor.authorTorroba Pérez, Tomás 
dc.date.accessioned2018-08-23T10:50:25Z
dc.date.available2018-08-23T10:50:25Z
dc.date.issued2013-02
dc.identifier.issn1477-0520
dc.identifier.urihttp://hdl.handle.net/10259/4878
dc.description.abstractComplementary regioselective synthesis of iminohydantoins from isocyanoacetamides controlled by the substituent on the amide group has been described. 4-Iminohydantoins were the major products when the starting materials were N-alkyl isocyanoamides, whereas 2-iminohydantoins were the major products with N-aryl isocyanoamides.en
dc.description.sponsorshipMinisterio de Ciencia e Innovación, Spain (Project CTQ2009-12631- BQU), Junta de Castilla y León, Consejería de Educación y Cultura y Fondo Social Europeo (Projects BU023A09 and GR170).en
dc.format.mimetypeapplication/pdf
dc.language.isoenges
dc.publisherRoyal Society of Chemistryen
dc.relation.ispartofOrganic & Biomolecular Chemistry. 2014, V. 11, n. 5, p. 721-725en
dc.subject.otherQuímica orgánicaes
dc.subject.otherChemistry, Organicen
dc.titleComplementary regioselectivity in the synthesis of iminohydantoins: remarkable effect of amide substitution on the cyclizationen
dc.typeinfo:eu-repo/semantics/article
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.relation.publisherversionhttps://doi.org/10.1039/C2OB27098F
dc.identifier.doi10.1039/C2OB27098F
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN/CTQ2009-12631- BQU
dc.relation.projectIDinfo:eu-repo/grantAgreement/JCyL/BU023A09
dc.relation.projectIDinfo:eu-repo/grantAgreement/JCyL/GR170
dc.type.hasVersioninfo:eu-repo/semantics/acceptedVersionen


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