Aiguabella Font, NúriaArce, Elsa M.Pozo, Carlos delVerdaguer i Espaulella, XavierRiera i Escalé, Antoni2014-05-222014-05-222014-02-031420-3049https://hdl.handle.net/2445/54408Abstract: The scope of the Pauson-Khand reaction (PKR) of internal trifluoromethyl alkynes, previously described with norbornadiene, is expanded to norbornene and ethylene. A thorough structural analysis of the resulting PK adducts has been carried out to unveil that α-trifluoromethylcyclopentenones are preferred in all cases, independently of the electronic properties of the alkyne. The regioselectivity observed with norbornadiene and ethylene is higher than in the case of norbornene.12 p.application/pdfengcc-by (c) Aiguabella Font, Núria et al., 2014http://creativecommons.org/licenses/by/3.0/esCiclització (Química)Química organometàl·licaCobaltRing formation (Chemistry)Organometallic chemistryCobaltPauson-Khand reaction of internal dissymmetric trifluoromethyl alkynes. influence of the alkene on the regioselectivityinfo:eu-repo/semantics/article6334582014-05-22info:eu-repo/semantics/openAccess24496269