Argitalpenak (79) MARIA LUZ CARDONA PROSPER argitalpenak

2022

  1. Cytotoxicity, Molecular Docking, ADMET and DFT Analysis of Alkaloids from the Roots and Fruits of Vepris dainelli

    Current Bioactive Compounds, Vol. 18, Núm. 8

  2. Cytotoxicity, antimicrobial activity, molecular docking, drug likeness and dft analysis of benzo[c]phenanthridine alkaloids from roots of zanthoxylum chalybeum

    Biointerface Research in Applied Chemistry, Vol. 12, Núm. 2, pp. 1569-1586

  3. Implementación de los ODS en las Asignaturas de Laboratorio de Química Orgánica en el Grado de Química de la UV

    In-Red 2022. VIII Congreso nacional de innovación educativa y docencia en red

2021

  1. Antimicrobial activity, in silico molecular docking, admet and dft analysis of secondary metabolites from roots of three ethiopian medicinal plants

    Advances and Applications in Bioinformatics and Chemistry, Vol. 14, pp. 117-132

  2. Chemical composition, cytotoxicity and larvicidal activity of essential oils of three medicinal plants of Ethiopian flora against anisakis L3 larvae

    Research Journal of Pharmacognosy, Vol. 8, Núm. 4, pp. 21-30

  3. Mg/BOX complexes as efficient catalysts for the enantioselective Michael addition of malonates to β-trifluoromethyl-α,β-unsaturated ketones and their N-tosyl imines

    Tetrahedron, Vol. 80

2019

  1. Asymmetric diastereodivergent Michael addition of 2-chloromalonate esters to conjugated imines enabled by catalyst metal change

    Organic Chemistry Frontiers, Vol. 6, Núm. 16, pp. 2907-2915

  2. Regio-, Diastereo-, and Enantioselective Organocatalytic Addition of 4-Substituted Pyrazolones to Isatin-Derived Nitroalkenes

    European Journal of Organic Chemistry, Vol. 2019, Núm. 19, pp. 3040-3044

2018

  1. Lanthanum-pyBOX complexes as catalysts for the enantioselective conjugate addition of malonate esters to β,γ-unsaturated α-ketimino esters

    Journal of Coordination Chemistry, Vol. 71, Núm. 6, pp. 864-873

2017

  1. Catalytic Asymmetric Formal [3+2] Cycloaddition of 2-Isocyanatomalonate Esters and Unsaturated Imines: Synthesis of Highly Substituted Chiral γ-Lactams

    Chemistry - A European Journal, Vol. 23, Núm. 59, pp. 14707-14711

  2. Copper-catalysed enantioselective Michael addition of malonic esters to β-Trifluoromethyl-α,β-unsaturated imines

    Organic and Biomolecular Chemistry, Vol. 15, Núm. 18, pp. 3849-3853

2016

  1. E,Z-Stereodivergent synthesis of N-tosyl α,β-dehydroamino esters via a Mukaiyama-Michael addition

    RSC Advances, Vol. 6, Núm. 19, pp. 15655-15659

2013

  1. Asymmetric CONJUGATE ADDITION of MALONATE ESTERS to α,β- UNSATURATED N-sulfonyl imines: An expeditious route to chiral δ-aminoesters and piperidones

    Chemistry - A European Journal, Vol. 19, Núm. 44, pp. 14861-14866

  2. Erratum: Asymmetric conjugate addition of malonate esters to α,β-unsaturated N-sulfonyl imines: An expeditious route to chiral δ-aminoesters and piperidones (Chem. Eur. J. (2013) 19 DOI: 10.1002/chem.201302687)

    Chemistry - A European Journal

2012

  1. Enantioselective zinc-mediated conjugate addition of terminal alkynes to enones

    Chemistry - A European Journal, Vol. 18, Núm. 41, pp. 12966-12969

  2. NMR spectroscopic characterization and DFT calculations of zirconium(IV)-3,3′-Br2a-BINOLate and related complexes used in an enantioselective friedela-crafts alkylation of indoles with α,β-unsaturated ketones

    Journal of Organic Chemistry, Vol. 77, Núm. 23, pp. 10545-10556

2011

  1. Exo-selective asymmetric inverse-electron demand hetero-diels-alder reaction catalyzed by Cu(II)-hydroxy oxazoline ligands

    Synlett, pp. 1592-1596

2009

  1. Catalytic enantioselective addition of terminal alkynes to aromatic aldehydes using zinc-hydroxyamide complexes

    Organic and Biomolecular Chemistry, Vol. 7, Núm. 20, pp. 4301-4308

2008

  1. Highly enantioselective zinc/binol-catalyzed alkynylation of N-sulfonyl aldimines

    Angewandte Chemie - International Edition, Vol. 47, Núm. 30, pp. 5593-5596

2007

  1. Cobalt(III) complex catalyzed aerobic oxidation of propargylic alcohols

    Synthesis, pp. 3329-3332