Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/127746
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dc.contributor.authorBrun Cubero, Omar-
dc.contributor.authorArchibald, L. J.-
dc.contributor.authorAgramunt, Jordi-
dc.contributor.authorPedroso Muller, Enrique-
dc.contributor.authorGrandas Sagarra, Anna-
dc.date.accessioned2019-01-30T17:40:13Z-
dc.date.available2019-01-30T17:40:13Z-
dc.date.issued2017-03-03-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://hdl.handle.net/2445/127746-
dc.description.abstractUnprotected linear peptides containing N-terminal cysteines and another cysteine residue can be simultaneously cyclized and derivatized using 2,2-disubstituted cyclopentenediones. High yields of cyclic peptide conjugates may be obtained in short reaction times using only a slight excess of the cyclopentenedione moiety under TEMPO catalysis and in the presence of LiCl.-
dc.format.extent4 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.orglett.6b03825-
dc.relation.ispartofOrganic Letters, 2017, vol. 19, num. 5, p. 992-995-
dc.relation.urihttps://doi.org/10.1021/acs.orglett.6b03825-
dc.rights(c) American Chemical Society , 2017-
dc.sourceArticles publicats en revistes (Química Inorgànica i Orgànica)-
dc.subject.classificationPèptids-
dc.subject.classificationCisteïna-
dc.subject.classificationEstructura molecular-
dc.subject.otherPeptides-
dc.subject.otherCysteine-
dc.subject.otherMolecular structure-
dc.titleSimultaneous cyclization and derivatization of peptides using cyclopentenediones-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec669149-
dc.date.updated2019-01-30T17:40:13Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid28212041-
Appears in Collections:Articles publicats en revistes (Química Inorgànica i Orgànica)

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