Simultaneous cyclization and derivatization of peptides using cyclopentenediones

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.date.updated2019-01-30T17:40:13Z
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.identifier.idgrec669149
dc.identifier.issn1523-7060
dc.identifier.pmid28212041
dc.identifier.urihttps://hdl.handle.net/2445/127746
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.rights.accessRightsinfo:eu-repo/semantics/openAccess
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

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