Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/50383
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dc.contributor.authorSánchez-Moya, Albert-
dc.contributor.authorPedroso Muller, Enrique-
dc.contributor.authorGrandas Sagarra, Anna-
dc.date.accessioned2014-02-18T15:19:49Z-
dc.date.available2014-12-31T23:02:05Z-
dc.date.issued2013-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/2445/50383-
dc.description.abstractA novel method to synthesize cyclic oligonucleotides (5- to 26-mer) using the thiol-maleimide reaction is described. The target molecules were obtained after subsequent removal of thiol and maleimide protecting groups from 5′-maleimido-3′-thiol-derivatized linear precursors. Retro-Diels-Alder conditions deprotecting the maleimide simultaneously promoted cyclization cleanly and in high yield.-
dc.format.extent3 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherRoyal Society of Chemistry-
dc.relation.isformatofVersió postprint del document publicat a: http://dx.doi.org/ 10.1039/C2CC35357A-
dc.relation.ispartofChemical Communications, 2013, vol. 49, p. 309-311-
dc.relation.urihttp://dx.doi.org/10.1039/C2CC35357A-
dc.rights(c) Sánchez, Albert et al., 2013-
dc.sourceArticles publicats en revistes (Química Inorgànica i Orgànica)-
dc.subject.classificationBioquímica-
dc.subject.classificationÀcids nucleics-
dc.subject.classificationBacteris-
dc.subject.classificationMicrobiologia-
dc.subject.classificationCiclització (Química)-
dc.subject.otherBiochemistry-
dc.subject.otherNucleic acids-
dc.subject.otherBacteria-
dc.subject.otherMicrobiology-
dc.subject.otherRing formation (Chemistry)-
dc.titleOligonucleotide cyclization: The thiol-maleimide reaction revisitedeng
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec619951-
dc.date.updated2014-02-18T11:02:41Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid23183555-
Appears in Collections:Articles publicats en revistes (Química Inorgànica i Orgànica)

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