Publications in collaboration with researchers from Universidad del País Vasco/Euskal Herriko Unibertsitatea (43)

2023

  1. Enantioselective C–C, C–halogen and C–H bond forming reactions promoted by organocatalysts based on non-proteinogenic α-amino acid derivatives

    Advances in Catalysis (Academic Press Inc.), pp. 143-210

  2. Remote Asymmetric Bisvinylogous [4+2] Cycloaddition Reaction to Synthesize Spirocyclic Frameworks

    Advanced Synthesis and Catalysis, Vol. 365, Núm. 19, pp. 3253-3259

2022

  1. Synthesis of Bicyclic Hemiacetals Catalyzed by Unnatural Densely Substituted γ-Dipeptides

    Journal of Organic Chemistry, Vol. 87, Núm. 21, pp. 14819-14824

2021

  1. Additive and Emergent Catalytic Properties of Dimeric Unnatural Amino Acid Derivatives: Aldol and Conjugate Additions

    Chemistry - A European Journal, Vol. 27, Núm. 63, pp. 15671-15687

  2. Biological properties and conformational studies of amphiphilic Pd(II) and Ni(II) complexes bearing functionalized aroylaminocarbo-N-thioylpyrrolinate units

    Beilstein Journal of Organic Chemistry, Vol. 17, pp. 2812-2821

2019

  1. From Bioactive Pyrrolidino[3,4- c ]pyrrolidines to more Bioactive Pyrrolidino[3,4- b ]pyrrolidines via Ring-Opening/Ring-Closing Promoted by Sodium Methoxide

    Synthesis (Germany), Vol. 51, Núm. 7, pp. 1565-1577

  2. Switching Diastereoselectivity in Catalytic Enantioselective (3+2) Cycloadditions of Azomethine Ylides Promoted by Metal Salts and Privileged Segphos-Derived Ligands

    Journal of Organic Chemistry, Vol. 84, Núm. 17, pp. 10593-10605

2018

  1. A Three-Component Enantioselective Cyclization Reaction Catalyzed by an Unnatural Amino Acid Derivative

    Angewandte Chemie - International Edition, Vol. 57, Núm. 3, pp. 668-672

  2. Cooperative Catalysis with Coupled Chiral Induction in 1,3-Dipolar Cycloadditions of Azomethine Ylides

    Chemistry - A European Journal, Vol. 24, Núm. 32, pp. 8092-8097

2017

  1. Diastereoselective [3 + 2] vs [4 + 2] Cycloadditions of Nitroprolinates with α,β-Unsaturated Aldehydes and Electrophilic Alkenes: An Example of Total Periselectivity

    Journal of Organic Chemistry, Vol. 82, Núm. 12, pp. 6298-6312

  2. Stereoselective Coupling of N-tert-Butanesulfinyl Aldimines and β-Keto Acids: Access to β-Amino Ketones

    Journal of Organic Chemistry, Vol. 82, Núm. 14, pp. 7481-7491

2016

  1. Bifunctional primary amine 2-aminobenzimidazole organocatalyst anchored to trans-cyclohexane-1,2-diamine in enantioselective conjugate additions of aldehydes

    Tetrahedron Asymmetry, Vol. 27, Núm. 2-3, pp. 118-122

  2. Enantioselective Synthesis of Polysubstituted Spiro-nitroprolinates Mediated by a (R,R)-Me-DuPhos·AgF-Catalyzed 1,3-Dipolar Cycloaddition

    Organic Letters, Vol. 18, Núm. 12, pp. 2926-2929

  3. Heterocycle-based bifunctional organocatalysts in asymmetric synthesis

    Pure and Applied Chemistry

  4. Taniaphos·AgF-catalyzed enantioselective 1,3-dipolar cycloaddition of stabilized azomethine ylides derived from 2,2-dimethoxyacetaldehyde

    Tetrahedron, Vol. 72, Núm. 40, pp. 6043-6051

2015

  1. Aromatic Esters of Bicyclic Amines as Antimicrobials against Streptococcus pneumoniae

    Angewandte Chemie - International Edition, Vol. 54, Núm. 46, pp. 13673-13677

  2. Densely substituted l -proline esters as catalysts for asymmetric michael additions of ketones to nitroalkenes

    Journal of Organic Chemistry, Vol. 80, Núm. 11, pp. 5588-5599

  3. Enantioselective Synthesis of exo -4-Nitroprolinates from Nitroalkenes and Azomethine Ylides Catalyzed by Chiral Phosphoramidite·Silver(I) or Copper(II) Complexes

    Synthesis (Germany), Vol. 47, Núm. 7, pp. 934-943

  4. Primary Amine-2-Aminopyrimidine Chiral Organocatalysts for the Enantioselective Conjugate Addition of Branched Aldehydes to Maleimides

    Synthesis (Germany), Vol. 47, Núm. 15, pp. 2199-2206

  5. Pyrimidine-derived prolinamides as recoverable bifunctional organocatalysts for enantioselective inter- and intramolecular aldol reactions under solvent-free conditions

    European Journal of Organic Chemistry, Vol. 2015, Núm. 12, pp. 2614-2621