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Comparison of Coated and Immobilized Chiral Stationary Phases Based on Amylose tris-[(S)-α-Methylbenzylcarbamate] for the HPLC Enantiomer Separation of α-Lipoic Acid and Its Reduced Form
Pubblicato su: Molecules (Basel, Switzerland)
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Chromatographic separation of the interconverting enantiomers of imidazo- and triazole-fused benzodiazepines
Pubblicato su: Journal of Chromatography A
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On-column quantification of amino functionalities bonded to solid porous matrices packed within high performance liquid chromatography columns
Pubblicato su: Journal of Chromatography A
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Molecular recognition of the hplc whelk-o1 selector towards the conformational enantiomers of nevirapine and oxcarbazepine
Pubblicato su: International Journal of Molecular Sciences
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Phenyl(thio)phosphon(amid)ate Benzenesulfonamides as Potent and Selective Inhibitors of Human Carbonic Anhydrases II and VII Counteract Allodynia in a Mouse Model of Oxaliplatin-Induced Neuropathy
Pubblicato su: Journal of Medicinal Chemistry
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Site-Directed Antibody Immobilization by Resorc[4]arene-Based Immunosensors
Pubblicato su: Chemistry - A European Journal
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1,3-Dipolar Cycloaddition, HPLC Enantioseparation, and Docking Studies of Saccharin/Isoxazole and Saccharin/Isoxazoline Derivatives as Selective Carbonic Anhydrase IX and XII Inhibitors
Pubblicato su: Journal of Medicinal Chemistry
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High-performance liquid chromatography enantioseparation of chiral 2-(benzylsulfinyl)benzamide derivatives on cellulose tris(3,5-dichlorophenylcarbamate) chiral stationary phase
Pubblicato su: Journal of Chromatography A
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Chiral (cyclopentadienone)iron complexes with a stereogenic plane as pre-catalysts for the asymmetric hydrogenation of polar double bonds
Pubblicato su: Tetrahedron
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Modular and conservative procedure for the quantification of amino functionalities bonded to solid porous matrices
Pubblicato su: Analytica Chimica Acta
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TetraPh-Tol-BITIOPO: a new atropisomeric 3,3′-bithiophene based phosphine oxide as an organocatalyst in Lewis base-catalyzed Lewis acid mediated reactions
Pubblicato su: Organic and Biomolecular Chemistry
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Recognition mechanism of aromatic derivatives resolved by argentation chromatography: The driving role played by substituent groups
Pubblicato su: Analytica Chimica Acta
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A chromatographic study on the retention behavior of the amylose tris(3-chloro-5-methylphenylcarbamate) chiral stationary phase under aqueous conditions
Pubblicato su: Journal of Separation Science
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Ionic Liquids as “Masking” Solvents of the Relative Strength of Bases in Proton Transfer Reactions
Pubblicato su: ChemPlusChem
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“Inherently Chiral” Ionic-Liquid Media: Effective Chiral Electroanalysis on Achiral Electrodes
Pubblicato su: Angewandte Chemie - International Edition
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BITHIENOLs: Promising C2-Symmetric Biheteroaromatic Diols for Organic Transformation
Pubblicato su: European Journal of Organic Chemistry
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3-(Phenyl-4-oxy)-5-phenyl-4;5-dihydro-(1H)-pyrazole: A fascinating molecular framework to study the enantioseparation ability of the amylose (3;5-dimethylphenylcarbamate) chiral stationary phase. Part II. Solvophobic effects in enantiorecognition process
Pubblicato su: Journal of Chromatography A
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Enantiomers of triclabendazole sulfoxide: Analytical and semipreparative HPLC separation; absolute configuration assignment; and transformation into sodium salt
Pubblicato su: Journal of Pharmaceutical and Biomedical Analysis
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Chiral Separations. Chiral Dynamic Chromatography in the Study of Stereolabile Compounds
Pubblicato su: Handbook of Advanced Chromatography/ Mass Spectrometry Techniques
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Enantiopure C1-symmetric N-heterocyclic carbene ligands from desymmetrized meso-1;2-diphenylethylenediamine: Application in ruthenium-catalyzed olefin metathesis
Pubblicato su: Catalysts
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Synthetic strategies to serine-proline chimeras: An overview
Pubblicato su: Current Bioactive Compounds
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Ultra-fast high-efficiency enantioseparations by means of a teicoplanin-based chiral stationary phase made on sub-2μm totally porous silica particles of narrow size distribution
Pubblicato su: Journal of Chromatography A
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3-(Phenyl-4-oxy)-5-phenyl-4;5-dihydro-(1H)-pyrazole: A fascinating molecular framework to study the enantioseparation ability of the amylose (3;5-dimethylphenylcarbamate) chiral stationary phase. Part I. Structure-enantioselectivity relationships
Pubblicato su: Journal of Chromatography A
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Elucidation of the mechanisms governing the thermal diastereomerization of bioactive chiral 1;3;4-thiadiazoline spiro-cyclohexyl derivatives towards their anancomeric stereoisomers
Pubblicato su: RSC Advances
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Efficient organic monoliths prepared by γ-radiation induced polymerization in the evaluation of histone deacetylase inhibitors by capillary(nano)-high performance liquid chromatography and ion trap mass spectrometry
Pubblicato su: Journal of Chromatography A
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