Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/165543
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dc.contributor.authorPrieur, Vanessa-
dc.contributor.authorRubio Martínez, Jaime-
dc.contributor.authorFont Bardia, Ma. Mercedes-
dc.contributor.authorGuillaumet, Gérald-
dc.contributor.authorPujol Dilmé, M. Dolors-
dc.date.accessioned2020-06-15T10:08:19Z-
dc.date.available2020-06-15T10:08:19Z-
dc.date.issued2014-02-02-
dc.identifier.issn1434-193X-
dc.identifier.urihttp://hdl.handle.net/2445/165543-
dc.description.abstractA new synthetic routes to the triaryl pyrrolo[2,3-d]pyrimidines from common 4,6-dichloropyrimidine have been developed. The triarylated compounds are synthesized by three cross-coupling reactions using three different catalysts. The introduction of C-6-aryl was allowed in two step process using Sonogashira conditions followed by intramolecular cyclization and the Suzuki-Miyaura conditions led the C-4 and C-5 diarylation. This sequence allows a flexible approach to the highly arylated pyrrolopyrimidines containing different aryl groups-
dc.format.extent31 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherWiley-VCH-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1002/ejoc.201301496-
dc.relation.ispartofEuropean Journal of Organic Chemistry, 2014, vol. 2014, num. 7, p. 1514-1524-
dc.relation.urihttps://doi.org/10.1002/ejoc.201301496-
dc.rights(c) Wiley-VCH, 2014-
dc.subject.classificationNitrogen-
dc.subject.classificationMicroones-
dc.subject.otherNitrogen-
dc.subject.otherMicrowaves-
dc.titleMicrowave-Assisted Synthesis of Substituted Pyrrolo[2,3-d]pyrimidines-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec636482-
dc.date.updated2020-06-15T10:08:19Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Mineralogia, Petrologia i Geologia Aplicada)

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