Publicaciones en colaboración con investigadoras/es de University of Oklahoma (79)

2021

  1. Software for the frontiers of quantum chemistry: An overview of developments in the Q-Chem 5 package

    Journal of Chemical Physics, Vol. 155, Núm. 8

2011

  1. Alkene selenenylation: A comprehensive analysis of relative reactivities, stereochemistry and asymmetric induction, and their comparisons with sulfenylation

    Beilstein Journal of Organic Chemistry, Vol. 7, pp. 744-758

  2. Self-Disproportionation of enantiomers via sublimation; new an truly green dimension in optical purification

    Current Organic Synthesis, Vol. 8, Núm. 2, pp. 310-317

2010

  1. Asymmetric synthesis of fluorine-containing amines, amino alcohols, α- and β-amino acids mediated by chiral sulfinyl group

    Journal of Fluorine Chemistry, Vol. 131, Núm. 2, pp. 127-139

  2. Biomimetic reductive amination under the continuous-flow reaction conditions

    Journal of Fluorine Chemistry, Vol. 131, Núm. 2, pp. 261-265

  3. Chirality-dependent sublimation of α-(trifluoromethyl)-lactic acid: Relative vapor pressures of racemic, eutectic, and enantiomerically pure forms, and vibrational spectroscopy of isolated (S,S) and (S,R) dimers

    Journal of Fluorine Chemistry, Vol. 131, Núm. 4, pp. 495-504

  4. Editorial

    Journal of Fluorine Chemistry

  5. First principle lattice energy calculations for enantiopure and racemic crystals of α-(trifluoromethyl)lactic acid: Is self-disproportionation of enantiomers controlled by thermodynamic stability of crystals?

    Journal of Fluorine Chemistry, Vol. 131, Núm. 4, pp. 461-466

  6. Fluorine chemistry in Ukraine

    Journal of Fluorine Chemistry

  7. Practical methods for the synthesis of symmetrically α,α- disubstituted α-amino acids

    Synthesis, pp. 2319-2344

  8. Rational application of self-disproportionation of enantiomers via sublimation - A novel methodological dimension for enantiomeric purifications

    Tetrahedron Asymmetry, Vol. 21, Núm. 11-12, pp. 1396-1400

  9. Self-disproportionation of enantiomers of 3,3,3-trifluorolactic acid amides via sublimation

    Journal of Fluorine Chemistry, Vol. 131, Núm. 2, pp. 266-269

  10. Self-disproportionation of enantiomers of isopropyl 3,3,3-(trifluoro)lactate via sublimation: Sublimation rates vs. enantiomeric composition

    Journal of Fluorine Chemistry, Vol. 131, Núm. 4, pp. 535-539

  11. Self-disproportionation of enantiomers of α-trifluoromethyl lactic acid amides via sublimation

    Journal of Fluorine Chemistry, Vol. 131, Núm. 4, pp. 540-544

  12. Towards modular design of chiroptically switchable molecules based on formation and cleavage of metal-ligand coordination bonds

    Synthesis, pp. 49-56

2009

  1. Concise asymmetric synthesis of configurationally stable 4-trifluoromethyl thalidomide

    Future Medicinal Chemistry, Vol. 1, Núm. 5, pp. 897-908

  2. Continuous-flow asymmetric biomimetic transamination

    Journal of Fluorine Chemistry, Vol. 130, Núm. 5, pp. 512-515

  3. Michael addition reactions between nucleophilic glycine equivalents and acrylic acid derivatives as a practical and generalized approach to the asymmetric synthesis of β-substituted-α-amino acids

    ACS Symposium Series

  4. Michael addition reactions between various nucleophilic glycine equivalents and (S,E)-1-enoyl-5-oxo-N-phenylpyrrolidine-2-carboxamide, an optimal type of chiral Michael acceptor in the asymmetric synthesis of β-phenyl pyroglutamic acid and related compounds

    Tetrahedron Asymmetry, Vol. 20, Núm. 22, pp. 2629-2634

  5. New generation of modular nucleophilic glycine equivalents for the general synthesis of α-amino acids

    Synlett, pp. 0704-0715