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dc.contributor.authorSenge, Mathiasen
dc.date.accessioned2019-12-03T15:39:33Z
dc.date.available2019-12-03T15:39:33Z
dc.date.issued2018en
dc.date.submitted2018en
dc.identifier.citationBernhard, S.S.R. and Locke, G.M. and Plunkett, S. and Meindl, A. and Flanagan, K.J. and Senge, M.O., Cubane Cross-Coupling and Cubane-Porphyrin Arrays, Chemistry - A European Journal, 24, 2018, 1026?1030.en
dc.identifier.otherYen
dc.descriptionPUBLISHEDen
dc.description.abstractHerein, an improved methodology for aryl‐cubane cross‐coupling is reported. The peculiarities of the cubane core and its behavior during cross‐coupling conditions were analyzed, while the versatility of this adapted Baran cross‐coupling methodology was demonstrated by the synthesis of various aryl‐cubane systems, including coupling products of cubanes and porphyrins. Furthermore, arm extension of alkynyl‐cubanes by Sonogashira reactions is demonstrated, showcasing the first proof of the stability of the cubane core in the presence of palladium catalysts.en
dc.format.extent1026?1030.en
dc.language.isoenen
dc.relation.ispartofseriesChemistry - A European Journalen
dc.relation.ispartofseries24en
dc.rightsYen
dc.subjectCross-couplingen
dc.subjectCubanesen
dc.subjectNickel catalysisen
dc.subjectPorphyrinoidsen
dc.subjectSonogashira couplingen
dc.titleCubane Cross-Coupling and Cubane-Porphyrin Arraysen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/sengemen
dc.identifier.rssinternalid181863en
dc.identifier.doihttp://dx.doi.org/10.1002/chem.201704344en
dc.rights.ecaccessrightsopenAccess
dc.contributor.sponsorScience Foundation Ireland (SFI)en
dc.contributor.sponsorGrantNumberFI IvP 13/IA/1894en
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/full/10.1002/chem.201704344
dc.identifier.urihttp://hdl.handle.net/2262/90956


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