Pedro José González Liste-rekin lankidetzan egindako argitalpenak (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