University of Strasbourg-ko ikertzaileekin lankidetzan egindako argitalpenak (12)

2009

  1. Application of the DFT Method to the Study of Intramolecular Palladium Shifts in Aryl and Polyaryl Complexes

    Computational Methods in Catalysis and Materials Science: An Introduction for Scientists and Engineers (Wiley-VCH Verlag GmbH & Co. KGaA), pp. 341-357

  2. Efficient, nickel-catalysed Kumada-Tamao-Corriu cross-coupling with a calix[4]arene-diphosphine ligand

    Advanced Synthesis and Catalysis, Vol. 351, Núm. 9, pp. 1383-1389

  3. Palladium motion in cyclomeric compounds: A theoretical study

    Inorganic Chemistry, Vol. 48, Núm. 23, pp. 11131-11141

2006

  1. Ethylene oligomerisation and polymerisation with nickel phosphanylenolates bearing electron-withdrawing substituents: Structure-reactivity relationships

    Chemistry - A European Journal, Vol. 12, Núm. 20, pp. 5210-5219

  2. Intramolecular 1,n palladium migrations in polycyclic aromatic hydrocarbons. Palladium(II) versus palladium(iv) mechanisms: A theoretical study

    Organometallics, Vol. 25, Núm. 13, pp. 3130-3142

2005

  1. Can weak interactions modify the binding properties of a strong nitrogen donor? Unusual N-coordination of a phosphoranylidene-substituted pyrazolone unit towards palladium(II) centres: An experimental and theoretical study

    Dalton Transactions, pp. 3155-3160

  2. Controlled synthesis of α-allenic ester and spiro ketone derivatives from tailored α-substituted cycloalkanones through cascade reactions: Exploring the possible reaction pathways by means of semiempirical MO calculations

    European Journal of Organic Chemistry, pp. 4346-4358

  3. Convenient synthesis of nucleoside and isonucleoside analogues

    Organic Letters, Vol. 7, Núm. 11, pp. 2161-2164

  4. Cyclocarbopalladation involving an unusual 1,5-palladium vinyl to aryl shift as termination step: Theoretical study of the mechanism

    Journal of the American Chemical Society, Vol. 127, Núm. 19, pp. 7171-7182

  5. Erratum: Semiempirical MO approach to the mechanism of the NIS-mediated nucleophilic addition to glycals: Multicomponent intermediates as models to tackle reactivity in organic chemistry (Tetrahedron: Asymmetry (2005) 16 (1615) DOI: 10.1016/j.tetasy.2005.03.010)

    Tetrahedron Asymmetry

  6. Semiempirical MO approach to the mechanism of the NIS-mediated nucleophilic addition to glycals: Multicomponent intermediates as models to tackle reactivity in organic chemistry

    Tetrahedron Asymmetry, Vol. 16, Núm. 9, pp. 1615-1629

2004

  1. Thermodynamic and kinetic considerations in the chemoselective O-acylation by mixed anhydrides. A semiempirical MO approach

    Tetrahedron Letters, Vol. 45, Núm. 17, pp. 3349-3353