Works matching DE "CHIRAL stationary phases"
Results: 612
Chiral Recognition Mechanism of Benzyltetrahydroisoquinoline Alkaloids: Cyclodextrin-Mediated Capillary Electrophoresis, Chiral HPLC, and NMR Spectroscopy Study.
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- Molecules, 2025, v. 30, n. 5, p. 1125, doi. 10.3390/molecules30051125
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Determination of the Enantiomerization Barrier of Midazolam in Aqueous Conditions by Electronic Circular Dichroism and Dynamic Enantioselective HPLC/UHPLC.
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- Molecules, 2025, v. 30, n. 5, p. 1108, doi. 10.3390/molecules30051108
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Chiral Separation and Determination of Enantiomer Elution Order of Novel Ketamine Derivatives Using CE-UV and HPLC-UV-ORD.
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- Separations (2297-8739), 2025, v. 12, n. 2, p. 44, doi. 10.3390/separations12020044
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Hydrophobic deep eutectic solvent-ferrofluid microextraction followed by liquid chromatography-mass spectrometry for the enantioselective determination of chiral agrochemicals in natural waters: Hydrophobic deep eutectic solvent-ferrofluid microextraction followed by liquid chromatography-mass spectrometry for the enantioselective determination of chiral agrochemicals in natural waters: Lucci et al
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- Analytical & Bioanalytical Chemistry, 2025, v. 417, n. 7, p. 1341, doi. 10.1007/s00216-024-05619-9
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Unrevealing the Nitrogen Elusive Chirality of 3‐Sulfanyl and 3‐Sulfinyl N‐Tosyl Isoindolinones by ECD Spectra: An Experimental and Theoretical Investigation.
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- Chemistry - A European Journal, 2024, v. 30, n. 29, p. 1, doi. 10.1002/chem.202400232
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Efficient Synthesis and Structural Analysis of Chiral 4,4′‐Biazulene.
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- Chemistry - A European Journal, 2024, v. 30, n. 24, p. 1, doi. 10.1002/chem.202400098
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Chiroptical Recognition of Carboxylates with Charge‐Neutral Double‐Stranded Zinc(II) Helicates.
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- Chemistry - A European Journal, 2023, v. 29, n. 61, p. 1, doi. 10.1002/chem.202301613
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One‐Handed Helical Polyacetylenes Bearing Axially‐Chiral 2‐Arylpyridyl‐N‐Oxide Units for Efficient Chromatographic Enantioseparation of Chiral Aromatic and Aliphatic Alcohols.
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- Angewandte Chemie, 2023, v. 135, n. 31, p. 1, doi. 10.1002/ange.202306252
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Multistate Aggregation‐Induced Chiroptical Properties of Enantiopure Disulfide‐Mediated Bispyrene Macrocycles.
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- Angewandte Chemie, 2023, v. 135, n. 29, p. 1, doi. 10.1002/ange.202304075
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Di‐2,7‐pyrenidecaphyrin(1.1.0.0.0.1.1.0.0.0) and Its Bis‐Organopalladium Complexes: Synthesis and Chiroptical Properties.
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- Angewandte Chemie, 2023, v. 135, n. 3, p. 1, doi. 10.1002/ange.202212770
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Monitoring Reaction Intermediates to Predict Enantioselectivity Using Mass Spectrometry**.
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- Angewandte Chemie, 2022, v. 134, n. 36, p. 1, doi. 10.1002/ange.202205720
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Rhodium(I) Complexes Bearing an Aryl‐Substituted 1,3,5‐Hexatriene Chain: Catalysts for Living Polymerization of Phenylacetylene and Potential Helical Chirality of 1,3,5‐Hexatrienes.
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- Angewandte Chemie, 2021, v. 133, n. 41, p. 22375, doi. 10.1002/ange.202108032
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Multinuclear Ag Clusters Sandwiched by Pt Complex Units: Fluxional Behavior and Chiral‐at‐Cluster Photoluminescence.
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- Angewandte Chemie, 2021, v. 133, n. 19, p. 10749, doi. 10.1002/ange.202101460
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Bright Long‐Lived Circularly Polarized Luminescence in Chiral Chromium(III) Complexes.
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- Angewandte Chemie, 2021, v. 133, n. 18, p. 10183, doi. 10.1002/ange.202101158
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Racemic Monomer‐Based One‐Handed Helical Polymer Recognizes Enantiomers through Auto‐Evolution of Its Helical Handedness Excess.
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- Angewandte Chemie, 2021, v. 133, n. 9, p. 4675, doi. 10.1002/ange.202014946
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Stimuli‐Responsive Particle‐Based Amphiphiles as Active Colloids Prepared by Anisotropic Click Chemistry.
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- Angewandte Chemie, 2020, v. 132, n. 23, p. 8987, doi. 10.1002/ange.202001423
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Covalent Organic Frameworks with Chirality Enriched by Biomolecules for Efficient Chiral Separation.
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- Angewandte Chemie, 2018, v. 130, n. 51, p. 16996, doi. 10.1002/ange.201810571
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Intramolecular enantiomerism as revealed from Raman optical activity spectrum.
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- Journal of Raman Spectroscopy, 2015, v. 46, n. 12, p. 1303, doi. 10.1002/jrs.4763
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Development of a Normal Phase Chiral HPLC Method for Analysis of Afoxolaner: Review.
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- Indian Journal of Basic & Applied Medical Research, 2023, v. 12, n. 2, p. 53, doi. 10.36855/IJBAMR/2022/98215.55620
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Validation of a Normal Phase Chiral HPLC Method for Analysis of Afoxolaner.
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- Indian Journal of Basic & Applied Medical Research, 2023, v. 12, n. 2, p. 39, doi. 10.36855/IJBAMR/2022/98215.55610
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Effect of mountain and sea level pasture on monoterpene composition in milk, curd and Ragusano cheese at 4 and 7 months of aging.
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- Journal of Animal Science, 2006, v. 84, p. 422
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Computational Quantum Chemical Study, Insilco Molecular Docking and ADMET Study of (3E,5E)-3,5-Bis((1H-Indol-3-yl)Methylene)-1-Benzylpiperidin-4-One Derivatives.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 6, p. 3807, doi. 10.1080/10406638.2023.2239984
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Liquid Chromatographic Separation of MM 302 Da Polycyclic Aromatic Hydrocarbons in Synthetic Mixtures Using Chiral Stationary Phase Material.
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- Analytical Letters, 2023, v. 56, n. 17, p. 2822, doi. 10.1080/00032719.2023.2185251
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Enantiomeric Separation of Chiral Triazole Pesticides by a mono-6-(4-Nitrophenyl)-ureido-β-cyclodextrin-Bonded Stationary Phase Using High-Performance Liquid Chromatography.
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- Analytical Letters, 2020, v. 53, n. 15, p. 2481, doi. 10.1080/00032719.2020.1745821
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Possibilities and limitations of computer assisted chiral HPLC method development for ozanimod on polysaccharide based chiral stationary phases.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-78415-1
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Altering the Stereoselectivity of Whole-Cell Biotransformations via the Physicochemical Parameters Impacting the Processes.
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- Catalysts (2073-4344), 2021, v. 11, n. 7, p. 781, doi. 10.3390/catal11070781
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Development of a Combined 2D-MGD TLC/HPTLC Method for the Separation of Terpinen-4-ol and α-Terpineol from Tea Tree, Melaleuca alternifolia , Essential Oil †.
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- Biomolecules (2218-273X), 2025, v. 15, n. 1, p. 147, doi. 10.3390/biom15010147
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Synthesis and HPLC-ECD Study of Cytostatic Condensed O,N-Heterocycles Obtained from 3-Aminoflavanones.
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- Biomolecules (2218-273X), 2020, v. 10, n. 10, p. 1462, doi. 10.3390/biom10101462
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NEW METHOD DEVELOPMENT AND VALIDATION FOR THE SIMULTANEOUS ESTIMATION OF CAPECITABINE AND GEMCITABINE BY USING RP-HPLC IN A BULK AND PHARMACEUTICAL DOAGE FORMS.
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- Pharma Science Monitor, 2017, v. 8, n. 2, p. 645
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SIMULTANEOUS ESTIMATION OF OFLOXACIN AND CEFPODOXIME PROXETIL IN TABLET DOSAGE FORM BY USING LIQUID CHROMATOGRAPHY METHODS.
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- Pharma Science Monitor, 2017, v. 8, n. 2, p. 573
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The Effect of the Stationary Phase on Resolution in the HPLC-Based Separation of Racemic Mixtures Using Vancomycin as a Chiral Selector: A Case Study with Profen Nonsteroidal Anti-Inflammatory Drugs.
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- Symmetry (20738994), 2023, v. 15, n. 12, p. 2154, doi. 10.3390/sym15122154
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Enantioseparation of β-Blockers Using Silica-Immobilised Eremomycin Derivatives as Chiral Stationary Phases in HPLC.
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- Symmetry (20738994), 2023, v. 15, n. 2, p. 373, doi. 10.3390/sym15020373
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Absolute Configuration of Aliphatic Hydrocarbon Enantiomers Identified by Gas Chromatography: Theorized Application for Isoprenoid Alkanes and the Search of Molecular Biosignatures on Mars.
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- Symmetry (20738994), 2022, v. 14, n. 2, p. N.PAG, doi. 10.3390/sym14020326
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Low Temperature Dynamic Chromatography for the Separation of the Interconverting Conformational Enantiomers of the Benzodiazepines Clonazolam, Flubromazolam, Diclazepam and Flurazepam.
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- Symmetry (20738994), 2021, v. 13, n. 6, p. 1012, doi. 10.3390/sym13061012
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Simultaneous Quantification of Mixed-Acid Triacylglycerol Positional Isomers and Enantiomers in Palm Oil and Lard by Chiral High-Performance Liquid Chromatography Coupled with Mass Spectrometry.
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- Symmetry (20738994), 2020, v. 12, n. 9, p. 1385, doi. 10.3390/sym12091385
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Venlafaxine Chiral Separation by Capillary Electrophoresis Using Cyclodextrin Derivatives as Chiral Selector and Experimental Design Method Optimization.
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- Symmetry (20738994), 2020, v. 12, n. 5, p. 849, doi. 10.3390/sym12050849
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Role of Geometric Shape in Chiral Optics.
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- Symmetry (20738994), 2020, v. 12, n. 1, p. 158, doi. 10.3390/sym12010158
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A General Phenomenon of Spontaneous Amplification of Optical Purity under Achiral Chromatographic Conditions.
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- Symmetry (20738994), 2019, v. 11, n. 5, p. 680, doi. 10.3390/sym11050680
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Chiral Stationary Phases for Liquid Chromatography Based on Chitin- and Chitosan-Derived Marine Polysaccharides.
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- Symmetry (20738994), 2017, v. 9, n. 9, p. 190, doi. 10.3390/sym9090190
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Chlorophylls, Symmetry, Chirality, and Photosynthesis.
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- Symmetry (20738994), 2014, v. 6, n. 3, p. 781, doi. 10.3390/sym6030781
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Supramolecular Chirality: Solvent Chirality Transfer in Molecular Chemistry and Polymer Chemistry.
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- Symmetry (20738994), 2014, v. 6, n. 3, p. 677, doi. 10.3390/sym6030677
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Separation of racemic mixtures of sn-1(3)-monoacylglycerols by enantioselective-HPLC/ELSD.
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- Journal of the American Oil Chemists' Society (JAOCS), 2021, v. 98, n. 11, p. 1035, doi. 10.1002/aocs.12538
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Synthesis of (<italic>R</italic>)‐ and (<italic>S</italic>)‐Ricinoleic Acid Amides and Evaluation of Their Antimicrobial Activity.
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- Journal of the American Oil Chemists' Society (JAOCS), 2018, v. 95, n. 1, p. 69, doi. 10.1002/aocs.12013
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Enantioselective Separation and Pharmacokinetics of a Chiral 1,4‐Dihydropyrimidine Derivative in Rats: A Combined Chromatography and Docking Approach.
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- Chirality, 2024, v. 36, n. 10, p. 1, doi. 10.1002/chir.23723
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Exploring a Lux® i‐Amylose‐3 column in normal phase and polar‐organic mode for chiral separation of cathinone derivatives and pyrovalerones using high‐performance liquid chromatography.
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- Chirality, 2024, v. 36, n. 5, p. 1, doi. 10.1002/chir.23679
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Screening of Astec® CHIRALDEX™ G‐PN and LIPODEX™ D gas chromatography columns for enantioseparation of amphetamine derivatives.
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- Chirality, 2024, v. 36, n. 5, p. 1, doi. 10.1002/chir.23676
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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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Chiral separations: Recent developments in chiral stationary phases and chromatographic separations of chiral compounds.
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- Chirality, 2024, v. 36, n. 3, p. 1, doi. 10.1002/chir.23657
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Investigation into the performance and stability of immobilized and coated polysaccharide columns in supercritical fluid chromatography.
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- Chirality, 2024, v. 36, n. 1, p. 1, doi. 10.1002/chir.23626
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Analytical and preparative chiral supercritical fluid chromatography resolutions using crown ether‐derived column.
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- Chirality, 2024, v. 36, n. 1, p. 1, doi. 10.1002/chir.23621
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