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dc.contributor.authorVega Ramiro, Juan Antonio 
dc.contributor.authorAlajarín Ferrández, Luis Ramón 
dc.contributor.authorVaquero López, Juan J.
dc.contributor.authorÁlvarez-Builla Gómez, Julio 
dc.date.accessioned2009-07-08T01:29:31Z
dc.date.available2009-07-08T01:29:31Z
dc.date.issued1998
dc.identifier.bibliographicCitationTetrahedron, 1998, v.54, n.14, p.3589-3606en
dc.identifier.issn0040-4020
dc.identifier.urihttp://hdl.handle.net/10017/3508
dc.description.abstractA series of N-alkyl-2-oxoalkanesulfonamides have been synthesized by reacting silyl enol ethers with N-alkyl-sulfamoyl chlorides. Their reactivity towards electrophiles was investigated in order to explore the regio-and stereoselectivity of the process. 2-Oxoalkanesulfonamides were used to prepare 5-(methylsulfamoyl)-1,4-dihydropyridines derivatives.en
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherPergamonen
dc.rights© Elsevier, 1998
dc.subjectSuifonamide groupen
dc.subjectStereoselectivityen
dc.subjectRadioselectivityen
dc.titleSynthesis and reactivity of N-alkyl-2-oxoalkanesulfonamidesen
dc.typeinfo:eu-repo/semantics/articleen
dc.subject.ecienciaCIENCIAes_ES
dc.subject.ecienciaQuímica orgánicaes_ES
dc.subject.ecienciaSCIENCEen
dc.subject.ecienciaChemistry, organicen
dc.contributor.affiliationUniversidad de Alcalá. Departamento de Química Orgánica
dc.relation.publisherversionhttp://dx.doi.org/10.1016/S0040-4020(98)00093-3
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1016/S0040-4020(98)00093-3
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen


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