Vadim A.
Soloshonok
University of Oklahoma
Norman, Estados UnidosPublicaciones en colaboración con investigadores/as de University of Oklahoma (78)
2011
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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
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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
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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
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Biomimetic reductive amination under the continuous-flow reaction conditions
Journal of Fluorine Chemistry, Vol. 131, Núm. 2, pp. 261-265
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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
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Editorial
Journal of Fluorine Chemistry
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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
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Fluorine chemistry in Ukraine
Journal of Fluorine Chemistry
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Practical methods for the synthesis of symmetrically α,α- disubstituted α-amino acids
Synthesis, pp. 2319-2344
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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
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Self-disproportionation of enantiomers of 3,3,3-trifluorolactic acid amides via sublimation
Journal of Fluorine Chemistry, Vol. 131, Núm. 2, pp. 266-269
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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
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Self-disproportionation of enantiomers of α-trifluoromethyl lactic acid amides via sublimation
Journal of Fluorine Chemistry, Vol. 131, Núm. 4, pp. 540-544
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Towards modular design of chiroptically switchable molecules based on formation and cleavage of metal-ligand coordination bonds
Synthesis, pp. 49-56
2009
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Concise asymmetric synthesis of configurationally stable 4-trifluoromethyl thalidomide
Future Medicinal Chemistry, Vol. 1, Núm. 5, pp. 897-908
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Continuous-flow asymmetric biomimetic transamination
Journal of Fluorine Chemistry, Vol. 130, Núm. 5, pp. 512-515
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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
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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
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New generation of modular nucleophilic glycine equivalents for the general synthesis of α-amino acids
Synlett, pp. 0704-0715
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New sterically driven mode for generation of helical chirality
Organic Letters, Vol. 11, Núm. 8, pp. 1797-1800