Publicaciones en las que colabora con Fernando Pedro Cossío Mora (23)

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

2019

  1. 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. 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. 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

  2. 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. 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

  2. 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

  3. Regio and diastereoselective multicomponent 1,3-dipolar cycloadditions between prolinate hydrochlorides, aldehydes and dipolarophiles for the direct synthesis of pyrrolizidines

    Tetrahedron, Vol. 71, Núm. 52, pp. 9645-9661

  4. Remote substituent effects on the stereoselectivity and organocatalytic activity of densely substituted unnatural proline esters in aldol reactions

    European Journal of Organic Chemistry, Vol. 2015, Núm. 11, pp. 2503-2516

  5. Synthesis of Chromen[4,3-b]pyrrolidines by Intramolecular 1,3-Dipolar Cycloadditions of Azomethine Ylides: An Experimental and Computational Assessment of the Origin of Stereocontrol

    European Journal of Organic Chemistry, Vol. 2015, Núm. 21, pp. 4689-4698

2014

  1. Efficient diastereo- and enantioselective synthesis of exo-nitroprolinates by 1,3-dipolar cycloadditions catalyzed by Chiral phosphoramidite·silver(I) complexes

    Advanced Synthesis and Catalysis, Vol. 356, Núm. 18, pp. 3861-3870

2013

  1. Phosphoramidite-Cu(OTf)2 complexes as chiral catalysts for 1,3-dipolar cycloaddition of iminoesters and nitroalkenes

    Organic Letters, Vol. 15, Núm. 12, pp. 2902-2905

  2. Synthetic scope and DFT analysis of the chiral binap-gold(I) complex-catalyzed 1,3-dipolar cycloaddition of azlactones with alkenes

    Beilstein Journal of Organic Chemistry, Vol. 9, pp. 2422-2433

2011

  1. Binap-gold(I) versus Binap-silver trifluoroacetate complexes as catalysts in 1,3-dipolar cycloadditions of azomethine ylides

    Chemistry - A European Journal, Vol. 17, Núm. 50, pp. 14224-14233

  2. Chiral gold(I) vs chiral silver complexes as catalysts for the enantioselective synthesis of the second generation GSK-hepatitis C virus inhibitor

    Beilstein Journal of Organic Chemistry, Vol. 7, pp. 988-996