Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/96758
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dc.creatorElías Quezada
dc.creatorDolores Viña
dc.creatorGiovanna Delogu
dc.creatorFernanda Borges
dc.creatorLourdes Santana
dc.creatorEugenio Uriarte
dc.date.accessioned2022-09-15T12:25:02Z-
dc.date.available2022-09-15T12:25:02Z-
dc.date.issued2010
dc.identifier.issn0018-019X
dc.identifier.othersigarra:49303
dc.identifier.urihttps://hdl.handle.net/10216/96758-
dc.description.abstractThe Mitsunobu reaction is an important tool in carbocyclic nucleoside chemistry for the direct coupling of alcohols with heterocyclic bases under mild conditions. Chemical evidences for an unusual competitive O2- vs. N1-alkylation of 3-substituted pyrimidines is presented.
dc.language.isoeng
dc.rightsrestrictedAccess
dc.subjectQuímica orgânica, Engenharia química
dc.subjectOrganic chemistry, Chemical engineering
dc.titleSynthesis of Carbocyclic Pyrimidine Nucleosides Using the Mitsunobu Reaction: O2- vs. N1-Alkylation
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoFaculdade de Ciências
dc.identifier.authenticusP-003-B34
dc.subject.fosCiências da engenharia e tecnologias::Engenharia química
dc.subject.fosEngineering and technology::Chemical engineering
Appears in Collections:FCUP - Artigo em Revista Científica Internacional

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