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dc.contributor.authorSánchez-Fernández, Elena M.es_ES
dc.contributor.authorRísquez-Cuadro, Rocioes_ES
dc.contributor.authorAguilar Moncayo, Matildees_ES
dc.contributor.authorGarcía Moreno, María Isabeles_ES
dc.contributor.authorOrtiz-Mellet, Carmenes_ES
dc.contributor.authorGarcía Fernández, José Manueles_ES
dc.date.accessioned2011-07-11T11:36:30Z-
dc.date.available2011-07-11T11:36:30Z-
dc.date.issued2009-07-16-
dc.identifier.citationOrganic Letters 11(15): 3306-3309 (2009)es_ES
dc.identifier.issn1523-7060-
dc.identifier.other19606851-
dc.identifier.urihttp://hdl.handle.net/10261/37657-
dc.description4 páginas, 2 figuras, 3 esquemas.es_ES
dc.description.abstractThe orbital (negative hyperconjugation) contribution to the generalized anomeric effect is highly increased in bicyclic gem-diamines with a pseudoamide-type endocyclic nitrogen atom, which has been exploited for the stereoselective synthesis of configurationally stable alpha-N-linked azadisaccharide heteroanalogues of the natural disaccharides maltose and isomaltose as aglycon-sensitive inhibitors of isomaltase.es_ES
dc.description.sponsorshipThis work was supported by the Spanish MEC (contract nos. CTQ2006-15515-C02-01/BQU and CTQ2007-61180/PPQ) and the Junta de Andalucía (P08-FQM-03711).es_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.rightsclosedAccesses_ES
dc.subjectDiamineses_ES
dc.subjectEnzyme inhibitorses_ES
dc.subjectGlucosaminees_ES
dc.subjectIsomaltosees_ES
dc.subjectMaltosees_ES
dc.subjectMolecular mimcryes_ES
dc.subjectStereoisomerismes_ES
dc.subjectGlycopyranosylaminees_ES
dc.subjectDisaccharidees_ES
dc.titleGeneralized Anomeric Effect in gem-Diamines: Stereoselective Synthesis of α-N-Linked Disaccharide Mimicses_ES
dc.typeartículoes_ES
dc.identifier.doi10.1021/ol901125n-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1021/ol901125nes_ES
dc.relation.csices_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.languageiso639-1en-
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