1. Dipòsit Digital de la Universitat de Barcelona
  2. Recerca
  3. Mineralogia, Petrologia i Geologia Aplicada
  4. Articles publicats en revistes (Mineralogia, Petrologia i Geologia Aplicada)
Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/164843
Full metadata record
DC FieldValueLanguage
dc.contributor.authorCamps García, Pelayo-
dc.contributor.authorLozano Mena, David-
dc.contributor.authorFont Bardia, Ma. Mercedes-
dc.date.accessioned2020-06-08T18:27:32Z-
dc.date.available2020-06-08T18:27:32Z-
dc.date.issued2015-06-22-
dc.identifier.issn1434-193X-
dc.identifier.urihttp://hdl.handle.net/2445/164843-
dc.description.abstractNew hexacyclo and octacyclo compounds have been synthesized by a short route whose key step consists of a single or double domino nucleophilic substitution of neopentyl‐type iodides with potassium cyclopentadienide, followed by intramolecular Diels-Alder cycloaddition.-
dc.format.extent24 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.201500601-
dc.relation.ispartofEuropean Journal of Organic Chemistry, 2015, vol. 2015, num. 22, p. 5013-5020-
dc.relation.urihttps://doi.org/10.1002/ejoc.201500601-
dc.rights(c) Wiley-VCH, 2015-
dc.sourceArticles publicats en revistes (Mineralogia, Petrologia i Geologia Aplicada)-
dc.subject.classificationReacció de Diels-Alder-
dc.subject.otherDiels-Alder reaction-
dc.titleSynthesis of polycycles by single or double domino nucleophilic substitution. Diels-Alder reaction-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec653816-
dc.date.updated2020-06-08T18:27:32Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Mineralogia, Petrologia i Geologia Aplicada)

Files in This Item:
File Description SizeFormat 
653816.pdf2.47 MBAdobe PDFView/Open
Show simple item record


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.