1. Dipòsit Digital de la Universitat de Barcelona
  2. Recerca
  3. Química Inorgànica i Orgànica
  4. Articles publicats en revistes (Química Inorgànica i Orgànica)
Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/160840
Full metadata record
DC FieldValueLanguage
dc.contributor.authorAgramunt, Jordi-
dc.contributor.authorGinesi, Rebecca-
dc.contributor.authorPedroso Muller, Enrique-
dc.contributor.authorGrandas Sagarra, Anna-
dc.date.accessioned2020-05-18T08:04:31Z-
dc.date.available2021-04-22T05:10:20Z-
dc.date.issued2020-04-22-
dc.identifier.issn0022-3263-
dc.identifier.urihttp://hdl.handle.net/2445/160840-
dc.description.abstractOligonucleotides, peptides, and peptide nucleic acids incorporating 7-oxanorbornene as a dienophile were reacted with tetrazines linked to either a peptide, d-biotin, BODIPY, or N-acetyl-d-galactosamine. The inverse electron-demand Diels-Alder (IEDDA) cycloaddition, which was performed overnight at 37 °C, in all cases furnished the target conjugate in good yields. IEDDA reactions with 7-oxanorbornenes produce a lower number of stereoisomers than that of IEDDA cycloadditions with other dienophiles.-
dc.format.extent12 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherAmerican Chemical Society-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1021/acs.joc.0c00583-
dc.relation.ispartofJournal of Organic Chemistry, 2020, vol. 85, num. 10, p. 6593-6604-
dc.relation.urihttps://doi.org/10.1021/acs.joc.0c00583-
dc.rights(c) American Chemical Society , 2020-
dc.sourceArticles publicats en revistes (Química Inorgànica i Orgànica)-
dc.subject.classificationSolucions (Química)-
dc.subject.classificationPèptids-
dc.subject.classificationProteïnes-
dc.subject.classificationBiopolímers-
dc.subject.classificationDissolvents-
dc.subject.otherSolution (Chemistry)-
dc.subject.otherPeptides-
dc.subject.otherProteins-
dc.subject.otherBiopolymers-
dc.subject.otherSolvents-
dc.titleInverse electron-demand Diels-Alder bioconjugation using 7-oxanorbornenes as dienophiles-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec700346-
dc.date.updated2020-05-18T08:04:31Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Química Inorgànica i Orgànica)

Files in This Item:
File Description SizeFormat 
700346.pdf1.05 MBAdobe PDFView/Open
Show simple item record


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.