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Synthesis and application of new iminopyridine ligands in the enantioselective palladium-catalyzed allylic alkylation

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Synthesis and application of new iminopyridine ligands in the enantioselective palladium-catalyzed allylic alkylation

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dc.contributor.author Solinas, Maurizio
dc.contributor.author Sechi, Barbara
dc.contributor.author Chelucci, Giorgio
dc.contributor.author Baldino, Salvatore
dc.contributor.author Pedro, José Ramón
dc.contributor.author Blay Llinares, Gonzalo
dc.date.accessioned 2014-02-26T09:11:17Z
dc.date.available 2014-02-26T09:11:17Z
dc.date.issued 2014
dc.identifier.citation Solinas, Maurizio Sechi, Barbara Chelucci, Giorgio Baldino, Salvatore Pedro, José Ramón Blay Llinares, Gonzalo 2014 Synthesis and application of new iminopyridine ligands in the enantioselective palladium-catalyzed allylic alkylation Journal of Molecular Catalysis A-Chemical 385 73 77
dc.identifier.uri http://hdl.handle.net/10550/33330
dc.description.abstract A variety of iminopyridines were obtained by condensation of chiral amines with pyridine-2-carboxaldehyde and quinoline-8-carbaldehyde, or of aminoalkylpyridine derivatives with chiral ketones. These ligands were assessed in the enantioselective palladium catalyzed allylic substitutionof 1,3-diphenylprop-2-enyl acetate with dimethyl malonate affording the product dimethyl 1,3-diphenylprop-2-enylmalonate in good yields and moderate enantioselectivities (up to 62% ee). Catalytic activity and enantioselectivity were found to be highly dependent upon the steric properties of the ligands. The best enantioselectivity (62% ee) was obtained by an iminopyridine based on a camphane skeleton.
dc.relation.ispartof Journal of Molecular Catalysis A-Chemical, 2014, vol. 385, p. 73-77
dc.subject Química
dc.title Synthesis and application of new iminopyridine ligands in the enantioselective palladium-catalyzed allylic alkylation
dc.type journal article es_ES
dc.date.updated 2014-02-26T09:11:17Z
dc.identifier.doi 10.1016/j.molcata.2014.01.006
dc.identifier.idgrec 093689
dc.rights.accessRights open access es_ES
dc.identifier.url 10.1016/j.molcata.2014.01.006

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