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Green HPLC Enantioseparation of Chemopreventive Chiral Isothiocyanates Homologs on an Immobilized Chiral Stationary Phase Based on Amylose tris-[(S)-α-Methylbenzylcarbamate].
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- Molecules, 2024, v. 29, n. 12, p. 2895, doi. 10.3390/molecules29122895
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- Article
Chiral Hydroxy Metabolite of Mebendazole: Analytical and Semi-Preparative High-Performance Liquid Chromatography Resolution and Chiroptical Properties.
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- Pharmaceuticals (14248247), 2024, v. 17, n. 6, p. 696, doi. 10.3390/ph17060696
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- Article
Enantioselective high‐performance liquid chromatography combined with spectroscopic methods and theoretical calculations: A valid strategy to determine the absolute configuration of eugenol derivatives.
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- Chirality, 2024, v. 36, n. 5, p. 1, doi. 10.1002/chir.23668
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- Article
Improving the Current European Pharmacopoeia Enantio-Selective HPLC Method for the Determination of Enantiomeric Purity in Atorvastatin Calcium Salt Drug Substance.
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- Separations (2297-8739), 2024, v. 11, n. 5, p. 154, doi. 10.3390/separations11050154
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- Article
Designing Powerful Biindole‐Based Inherently Chiral Selectors: Enhancing Enantiodiscrimination by Core Functionalization with Additional Coordination Elements.
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- Chemistry - A European Journal, 2024, v. 30, n. 23, p. 1, doi. 10.1002/chem.202303530
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- Article
A New Ultra High-Performance Liquid Chromatography-Tandem Mass Spectrometry Method to Monitor 1-Amino-4-Methyl-Piperazine and 1-Methyl-4-Nitroso-Piperazine in Rifampicin Hydrolysis: A Standard Addition Approach to Quantify Nitrosamine in Rifampicin.
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- Separations (2297-8739), 2024, v. 11, n. 2, p. 54, doi. 10.3390/separations11020054
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- Article
Kinetic Study on the Base-Catalyzed Imine-Enamine Tautomerism of a Chiral Biologically Active Isoxazoline Derivative by HPLC on Amylose Tris(3,5-dimethylphenylcarbamate) Chiral Stationary Phase.
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- Molecules, 2023, v. 28, n. 18, p. 6518, doi. 10.3390/molecules28186518
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- Article
Evaluation of the Stereochemical Lability of Benzo‐Cycloheptene‐Based Drugs Endowed with Potentially Modulable Planar Chirality.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 33, p. 1, doi. 10.1002/ejoc.202300568
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- Article
A New C 2 -Symmetric Atropisomeric Thiophene-Based Monomer for Inherently Chiral Electroactive Materials: Synthesis, HPLC Resolution, and Absolute Configuration Assignment.
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- Applied Sciences (2076-3417), 2023, v. 13, n. 3, p. 1407, doi. 10.3390/app13031407
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- Article
Bipolar Electrochemical Analysis of Chirality in Complex Media through Miniaturized Stereoselective Light-Emitting Systems.
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- Chemosensors, 2023, v. 11, n. 2, p. 131, doi. 10.3390/chemosensors11020131
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- Article
Cover Image, Volume 35, Issue 2.
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- Chirality, 2023, v. 35, n. 2, p. 1, doi. 10.1002/chir.23533
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- Article
Wireless electromechanical enantio‐responsive valves.
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- Chirality, 2023, v. 35, n. 2, p. 110, doi. 10.1002/chir.23521
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- Article
A Novel Validated UHPLC Method for the Estimation of Rosuvastatin and Its Complete Impurity Profile in Tablet Formulations.
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- Molecules, 2023, v. 28, n. 1, p. 431, doi. 10.3390/molecules28010431
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- Article
HPLC Enantioseparation of Rigid Chiral Probes with Central, Axial, Helical, and Planar Stereogenicity on an Amylose (3,5-Dimethylphenylcarbamate) Chiral Stationary Phase.
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- Molecules, 2022, v. 27, n. 23, p. 8527, doi. 10.3390/molecules27238527
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- Article
Autonomous Chiral Microswimmers with Self‐mixing Capabilities for Highly Efficient Enantioselective Synthesis.
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- Angewandte Chemie, 2022, v. 134, n. 40, p. 1, doi. 10.1002/ange.202209098
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- Article
Autonomous Chiral Microswimmers with Self‐mixing Capabilities for Highly Efficient Enantioselective Synthesis.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 40, p. 1, doi. 10.1002/anie.202209098
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- Article
Single‐run chemo‐ and enantio‐selective high‐performance liquid chromatography separation of tramadol and its principal metabolite, O‐desmethyltramadol, using a chlorinated immobilized amylose‐based chiral stationary phase under multimodal elution conditions
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- Separation Science Plus, 2022, v. 5, n. 5, p. 99, doi. 10.1002/sscp.202200009
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- Article
Trópos and Átropos Biindole Chiral Electroactive Monomers: A Voltammetry and HPLC Comparative Insight.
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- ChemElectroChem, 2022, v. 9, n. 6, p. 1, doi. 10.1002/celc.202100903
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- Article
Cover Feature: Trópos and Átropos Biindole Chiral Electroactive Monomers: A Voltammetry and HPLC Comparative Insight (ChemElectroChem 6/2022).
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- ChemElectroChem, 2022, v. 9, n. 6, p. 1, doi. 10.1002/celc.202200132
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- Article
Anticancer Activity of (S)-5-Chloro-3-((3,5-dimethylphenyl)sulfonyl)- N -(1-oxo-1-((pyridin-4-ylmethyl)amino)propan-2-yl)-1 H -indole-2-carboxamide (RS4690), a New Dishevelled 1 Inhibitor.
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- Cancers, 2022, v. 14, n. 5, p. 1358, doi. 10.3390/cancers14051358
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- Article
Enantioselective HPLC analysis of escitalopram oxalate and its impurities using a cellulose‐based chiral stationary phase under normal‐ and green reversed‐phase conditions.
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- Journal of Separation Science, 2022, v. 45, n. 5, p. 1059, doi. 10.1002/jssc.202100913
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- Article
Featured Cover.
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- Chirality, 2021, v. 33, n. 12, p. i, doi. 10.1002/chir.23398
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- Article
Hybrid light‐emitting devices for the straightforward readout of chiral information.
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- Chirality, 2021, v. 33, n. 12, p. 875, doi. 10.1002/chir.23370
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- Article
Triptycene derivatives as chiral probes for studying the molecular enantiorecognition on sub‐2‐μm particle cellulose tris(3,5‐dimethylphenylcarbamate) chiral stationary phase.
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- Chirality, 2021, v. 33, n. 12, p. 883, doi. 10.1002/chir.23358
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- Article
Modulating the Enantiodiscrimination Features of Inherently Chiral Selectors by Molecular Design: A HPLC and Voltammetry Study Case with Atropisomeric 2,2'‐Biindole‐Based Monomers and Oligomer Films.
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- Chemistry - A European Journal, 2021, v. 27, n. 52, p. 13190, doi. 10.1002/chem.202101170
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- Article
Cover Feature: In Situ Electrochemical Investigations of Inherently Chiral 2,2′‐Biindole Architectures with Oligothiophene Terminals (ChemElectroChem 17/2021).
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- ChemElectroChem, 2021, v. 8, n. 17, p. 3204, doi. 10.1002/celc.202100989
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- Article
In Situ Electrochemical Investigations of Inherently Chiral 2,2′‐Biindole Architectures with Oligothiophene Terminals.
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- ChemElectroChem, 2021, v. 8, n. 17, p. 3250, doi. 10.1002/celc.202100511
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- Article
2,12-Diaza[6]helicene: An Efficient Non-Conventional Stereogenic Scaffold for Enantioselective Electrochemical Interphases.
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- Chemosensors, 2021, v. 9, n. 8, p. 216, doi. 10.3390/chemosensors9080216
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- Article
PHANE-TetraPHOS, the First D<sub>2</sub> Symmetric Chiral Tetraphosphane. Synthesis, Metal Complexation, and Application in Homogeneous Stereoselective Hydrogenation.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 17, p. 2367, doi. 10.1002/ejoc.202100109
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- Article
Multimilligram‐scale production implementation of atropisomers of 2,2′‐bis(2,2′‐bithiophene‐5‐yl)‐3,3′‐bithianaphthene.
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- Chirality, 2021, v. 33, n. 4, p. 146, doi. 10.1002/chir.23294
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- Article
Screening of Benzimidazole-Based Anthelmintics and Their Enantiomers as Repurposed Drug Candidates in Cancer Therapy.
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- Pharmaceuticals (14248247), 2021, v. 14, n. 4, p. 372, doi. 10.3390/ph14040372
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- Publication type:
- Article
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.
- Published in:
- Molecules, 2021, v. 26, n. 6, p. 1747, doi. 10.3390/molecules26061747
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- Article
Helicity: A Non-Conventional Stereogenic Element for Designing Inherently Chiral Ionic Liquids for Electrochemical Enantiodifferentiation.
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- Molecules, 2021, v. 26, n. 2, p. 311, doi. 10.3390/molecules26020311
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- Article
Characterization of Inherently Chiral Electrosynthesized Oligomeric Films by Voltammetry and Scanning Electrochemical Microscopy (SECM).
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- Molecules, 2020, v. 25, n. 22, p. 5368, doi. 10.3390/molecules25225368
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- Article
Widening the Scope of "Inherently Chiral" Electrodes: Enantiodiscrimination of Chiral Electroactive Probes with Planar Stereogenicity.
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- ChemElectroChem, 2020, v. 7, n. 16, p. 3382, doi. 10.1002/celc.202000891
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- Article
Widening the Scope of "Inherently Chiral" Electrodes: Enantiodiscrimination of Chiral Electroactive Probes with Planar Stereogenicity.
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- ChemElectroChem, 2020, v. 7, n. 16, p. 3429, doi. 10.1002/celc.202000657
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- Article
Direct separation of the enantiomers of ramosetron on a chlorinated cellulose‐based chiral stationary phase in hydrophilic interaction liquid chromatography mode.
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- Journal of Separation Science, 2020, v. 43, n. 13, p. 2589, doi. 10.1002/jssc.202000290
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- Article
Self‐Standing Membranes Consisting of Inherently Chiral Electroactive Oligomers: Electrosynthesis, Characterization and Preliminary Tests in Potentiometric Setups.
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- ChemElectroChem, 2019, v. 6, n. 16, p. 4204, doi. 10.1002/celc.201900779
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- Article
Design, Synthesis, Docking Studies and Monoamine Oxidase Inhibition of a Small Library of 1-acetyl- and 1-thiocarbamoyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazoles.
- Published in:
- Molecules, 2019, v. 24, n. 3, p. 484, doi. 10.3390/molecules24030484
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- Article
A chromatographic study on the retention behavior of the amylose tris(3‐chloro‐5‐methylphenylcarbamate) chiral stationary phase under aqueous conditions.
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- Journal of Separation Science, 2018, v. 41, n. 21, p. 4014, doi. 10.1002/jssc.201800696
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- Article
Searching for Models Exhibiting High Circularly Polarized Luminescence: Electroactive Inherently Chiral Oligothiophenes.
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- Chemistry - A European Journal, 2018, v. 24, n. 43, p. 11082, doi. 10.1002/chem.201801158
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- Article
Progress in the pharmacological treatment of human cystic and alveolar echinococcosis: Compounds and therapeutic targets.
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- PLoS Neglected Tropical Diseases, 2018, v. 12, n. 4, p. 1, doi. 10.1371/journal.pntd.0006422
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- Article
Development of a high‐performance liquid chromatography method for the simultaneous determination of chiral impurities and assay of (<italic>S</italic>)‐clopidogrel using a cellulose‐based chiral stationary phase in methanol/water mode.
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- Journal of Separation Science, 2018, v. 41, n. 6, p. 1208, doi. 10.1002/jssc.201701191
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- Article
Erratum to: 'Inherently chiral' thiophene-based electrodes at work: a screening of enantioselection ability toward a series of pharmaceutically relevant phenolic or catecholic amino acids, amino esters, and amine.
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- 2017
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- Erratum
'Inherently Chiral' Ionic-Liquid Media: Effective Chiral Electroanalysis on Achiral Electrodes.
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- Angewandte Chemie, 2017, v. 129, n. 8, p. 2111, doi. 10.1002/ange.201607344
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- Article
Rücktitelbild: 'Inherently Chiral' Ionic-Liquid Media: Effective Chiral Electroanalysis on Achiral Electrodes (Angew. Chem. 8/2017).
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- Angewandte Chemie, 2017, v. 129, n. 8, p. 2254, doi. 10.1002/ange.201700414
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- Publication type:
- Article
'Inherently Chiral' Ionic-Liquid Media: Effective Chiral Electroanalysis on Achiral Electrodes.
- Published in:
- Angewandte Chemie International Edition, 2017, v. 56, n. 8, p. 2079, doi. 10.1002/anie.201607344
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- Article
Back Cover: 'Inherently Chiral' Ionic-Liquid Media: Effective Chiral Electroanalysis on Achiral Electrodes (Angew. Chem. Int. Ed. 8/2017).
- Published in:
- Angewandte Chemie International Edition, 2017, v. 56, n. 8, p. 2218, doi. 10.1002/anie.201700414
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- Publication type:
- Article
'Inherently chiral' thiophene-based electrodes at work: a screening of enantioselection ability toward a series of pharmaceutically relevant phenolic or catecholic amino acids, amino esters, and amine.
- Published in:
- Analytical & Bioanalytical Chemistry, 2016, v. 408, n. 26, p. 7243, doi. 10.1007/s00216-016-9852-x
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- Article
Cover Picture: Inherently Chiral Spider-Like Oligothiophenes (Chem. Eur. J. 31/2016).
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- Chemistry - A European Journal, 2016, v. 22, n. 31, p. 10681, doi. 10.1002/chem.201602280
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- Article