Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/54698
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dc.contributor.authorBruno, Paolo-
dc.contributor.authorPeña, Stella-
dc.contributor.authorJust Baringo, Xavier-
dc.contributor.authorAlbericio Palomera, Fernando-
dc.contributor.authorÁlvarez Domingo, Mercedes-
dc.date.accessioned2014-05-30T11:50:37Z-
dc.date.available2014-05-30T11:50:37Z-
dc.date.issued2011-08-03-
dc.identifier.issn1523-7060-
dc.identifier.urihttp://hdl.handle.net/2445/54698-
dc.description.abstractThe first total synthesis of Aeruginazole A, prepared via a convergent strategy that involved both solid-phase peptide synthesis and solution phase chemistry and that enabled conservation of the stereochemistry of the intermediates, is reported.-
dc.format.extent4 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherAmerican Chemical Society-
dc.relation.isformatofVersió postprint del document publicat a: http://dx.doi.org/10.1021/ol2018592-
dc.relation.ispartofOrganic Letters, 2011, vol. 13, num. 17, p. 4648-4651-
dc.relation.urihttp://dx.doi.org/10.1021/ol2018592-
dc.rights(c) American Chemical Society , 2011-
dc.sourceArticles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)-
dc.subject.classificationSíntesi de pèptids-
dc.subject.classificationQuímica heterocíclica-
dc.subject.otherPeptide synthesis-
dc.subject.otherHeterocyclic chemistry-
dc.titleTotal synthesis of aeruginazole A-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec598513-
dc.date.updated2014-05-30T11:50:37Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)

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