Publicaciones en colaboración con investigadoras/es de Universitat d'Alacant (23)

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

2020

  1. Nitroprolinates as Nucleophiles in Michael-type Additions and Acylations. Synthesis of Enantiomerically Enriched Fused Amino-pyrrolidino-[1,2-a]pyrazinones and -diketopiperazines

    ChemCatChem, Vol. 12, Núm. 7, pp. 2014-2021

2019

  1. Design, synthesis and amplified spontaneous emission of 1,2,5-benzothiadiazole derivatives

    Journal of Materials Chemistry C, Vol. 7, Núm. 32, pp. 9996-10007

  2. 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

  3. 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. 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

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. 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

  2. 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

  3. 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

  4. 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

2010

  1. Microwave-assisted stille reactions as a powerful tool for building polyheteroaryl systems bearing a (1H)-1,2,4-triazole moiety

    Synlett, pp. 55-60