Publications by the researcher in collaboration with Pedro José González Liste (12)

2017

  1. Broad Scope Synthesis of Ester Precursors of Nonfunctionalized Chiral Alcohols Based on the Asymmetric Hydrogenation of α,β-Dialkyl-, α,β-Diaryl-, and α-Alkyl-β-aryl-vinyl Esters

    Journal of Organic Chemistry, Vol. 82, Núm. 11, pp. 5852-5867

  2. Gold(i)-catalyzed addition of carboxylic acids to internal alkynes in aqueous medium

    Organic and Biomolecular Chemistry, Vol. 15, Núm. 7, pp. 1670-1679

  3. Gold-Catalyzed Regio- and Stereoselective Addition of Carboxylic Acids to Iodoalkynes: Access to (Z)-β-Iodoenol Esters and 1,4-Disubstituted (Z)-Enynyl Esters

    Journal of Organic Chemistry, Vol. 82, Núm. 3, pp. 1507-1516

  4. The intermolecular hydro-oxycarbonylation of internal alkynes: Current state of the art

    Arkivoc, Vol. 2018, Núm. 2, pp. 17-39

2016

  1. Bis(allyl)-ruthenium(IV) complexes with phosphinous acid ligands as catalysts for nitrile hydration reactions

    Dalton Transactions, Vol. 45, Núm. 34, pp. 13590-13603

  2. Chlorophosphines as auxiliary ligands in ruthenium-catalyzed nitrile hydration reactions: Application to the preparation of β-ketoamides

    Catalysis Science and Technology, Vol. 6, Núm. 12, pp. 4398-4409

  3. Half-Sandwich Guanidinate-Osmium(II) Complexes: Synthesis and Application in the Selective Dehydration of Aldoximes

    European Journal of Inorganic Chemistry, Vol. 2016, Núm. 3, pp. 393-402

  4. Highly Stereoselective Synthesis and Hydrogenation of (Z)-1-Alkyl-2-arylvinyl Acetates: A Wide Scope Procedure for the Preparation of Chiral Homobenzylic Esters

    ACS Catalysis, Vol. 6, Núm. 5, pp. 3056-3060

2015

  1. Catalytic Rearrangement of Aldoximes to Primary Amides in Environmentally Friendly Media under Thermal and Microwave Heating: Another Application of the Bis(allyl)-Ruthenium(IV) Dimer [{RuCl(μ-Cl)(η3:η3-C10H16)}2]

    ACS Sustainable Chemistry and Engineering, Vol. 3, Núm. 11, pp. 3004-3011

2014

  1. Asymmetric hydrogenation of 1-alkyl and 1-aryl vinyl benzoates: A broad scope procedure for the highly enantioselective synthesis of 1-substituted ethyl benzoates

    ACS Catalysis, Vol. 4, Núm. 12, pp. 4398-4408

  2. Erratum: Highly Enantioselective Hydrogenation of 1-Alkylvinyl Benzoates: A Simple, Nonenzymatic Access to Chiral 2-Alkanols (Chemistry - A European Journal (2013) 19 DOI: 10.1002/chem.201303500)

    Chemistry - A European Journal

2013

  1. Highly enantioselective hydrogenation of 1-alkylvinyl benzoates: A simple, nonenzymatic access to chiral 2-alkanols

    Chemistry - A European Journal, Vol. 19, Núm. 48, pp. 16209-16212