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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 |