Publicacións nas que colabora con VICTORIO CADIERNO MENENDEZ (93)

2010

  1. Access to the first (iminophosphoranyl)(selenophosphoranyl)methane ligands Ph2P(Se)CH2P(NR)Ph2: Coordination of their methanide and methandiide anions to ruthenium

    Dalton Transactions, Vol. 39, Núm. 3, pp. 941-956

  2. Atom-economic transformations of propargylic alcohols catalyzed by the 16-electron allyl-ruthenium(II) complex [Ru(η3-2-C3H4Me)(CO)(dppf)][SbF6] (dppf = 1,1′-bis(diphenylphosphino)ferrocene)

    Inorganica Chimica Acta, Vol. 363, Núm. 9, pp. 1912-1934

  3. Bis(allyl)ruthenium(rV) complexes containing water-soluble phosphane ligands: Synthesis, structure, and application as catalysts in the Selective hydration of organonitriles into amides

    Chemistry - A European Journal, Vol. 16, Núm. 32, pp. 9808-9817

  4. Cationic rhodium(I)-diolefin complexes containing an optically active C2-symmetric bis(sulfoximine) ligand: Synthesis and catalytic activity

    Polyhedron, Vol. 29, Núm. 18, pp. 3380-3386

  5. Metal-catalyzed transformations of propargylic alcohols into α,β-unsaturated carbonyl compounds: From the Meyer-Schuster and Rupe rearrangements to redox isomerizations

    Dalton Transactions, Vol. 39, Núm. 17, pp. 4015-4031

  6. Novel push-pull butadienes derived from 1,1-diaryl-2-propyn-1-ols and 1,1,1,5,5,5-hexafluoro-2,4-pentanedione: Synthesis, absorption spectra and solvatochromic behaviour

    Dyes and Pigments, Vol. 87, Núm. 3, pp. 209-217

  7. One-Pot Synthesis of Bicyclic Fused Cyclopentenone Derivatives from 1-Ethynylcycloalkanols and Aldehydes

    ChemCatChem, Vol. 2, Núm. 5, pp. 519-522

  8. One-pot three-component synthesis of tetrasubstituted N - H pyrroles from secondary propargylic alcohols, 1,3-dicarbonyl compounds and tert-butyl carbamate

    Journal of Heterocyclic Chemistry, Vol. 47, Núm. 1, pp. 233-236

  9. Ruthenium-catalyzed synthesis of β-oxo esters in aqueous medium: Scope and limitations

    Green Chemistry, Vol. 12, Núm. 1, pp. 135-143

  10. Ruthenium/TFA-catalyzed regioselective C-3-alkylation of indoles with terminal alkynes in water: Efficient and unprecedented access to 3-(1-methylalkyl)-1H-indoles

    Chemical Communications, Vol. 46, Núm. 23, pp. 4175-4177