Works matching DE "ENANTIOMERS analysis"
Results: 68
Multifunctional organoboron compounds for scalable natural product synthesis.
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- Nature, 2014, v. 513, n. 7518, p. 367, doi. 10.1038/nature13735
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Organic chemistry: Reactivity tamed one bond at a time.
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- Nature, 2014, v. 513, n. 7518, p. 324, doi. 10.1038/513324a
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Chiral analysis of amphetamine, methamphetamine, MDMA and MDA enantiomers in human hair samples.
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- Journal of Analytical Toxicology, 2024, v. 48, n. 4, p. 226, doi. 10.1093/jat/bkae026
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Chiral Analysis of Methadone and its Main Metabolite, EDDP, in Postmortem Brain and Blood by Automated SPE and Liquid Chromatography-Mass Spectrometry.
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- Journal of Analytical Toxicology, 2012, v. 36, n. 7, p. 487, doi. 10.1093/jat/bks057
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In Situ Aggregates of Enantiomeric Poly(styrene)- block-Poly(lactide) Diblock Copolymers via Stereocomplexation in a Non-selective Solvent.
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- Macromolecular Chemistry & Physics, 2013, v. 214, n. 14, p. 1569, doi. 10.1002/macp.201300216
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Comment on Hu et al. Determination of 2-Pentanol Enantiomers via Chiral GC-MS and Its Sensory Evaluation in Baijiu. Foods 2022, 11 , 2584.
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- Foods, 2023, v. 12, n. 7, p. 1449, doi. 10.3390/foods12071449
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Qualitative and Quantitative Analyses of the Enantiomers of Nicotine and Nornicotine Employing Chiral Supercritical Fluid Chromatography.
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- Journal of Chromatographic Science, 2024, v. 62, n. 5, p. 492, doi. 10.1093/chromsci/bmad048
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Preparation and Enantioseparation Characteristics of a Novel β-Cyclodextrin Derivative Chiral Stationary Phase in High-Performance Liquid Chromatography.
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- Journal of Chromatographic Science, 2015, v. 53, n. 5, p. 676, doi. 10.1093/chromsci/bmu099
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Synthesis, lipase catalyzed kinetic resolution, and determination of the absolute configuration of enantiomers of the Morita-Baylis-Hillman adduct 3- hydroxy-2-methylenebutanenitrile.
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- ARKIVOC: Online Journal of Organic Chemistry, 2017, v. 2017, p. 313, doi. 10.3998/ark.5550190.p009.749
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Larger laboratory scale synthesis of 5-methyluridine and formal synthesis of its L-enantiomer.
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- ARKIVOC: Online Journal of Organic Chemistry, 2017, v. 2017, p. 249, doi. 10.3998/ark.5550190.0018.400
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Enantioselective residue analysis of oxathiapiprolin and its metabolite in tea and other crops by ultra‐high performance liquid chromatography–tandem mass spectrometry.
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- Journal of Separation Science, 2020, v. 43, n. 20, p. 3856, doi. 10.1002/jssc.202000457
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Simultaneous determination of enantiomers of carfentrazone‐ethyl and its metabolite in eight matrices using high‐performance liquid chromatography with tandem mass spectrometry.
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- Journal of Separation Science, 2018, v. 41, n. 19, p. 3697, doi. 10.1002/jssc.201701349
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Simultaneous enantioselective determination of six pesticides in aqueous environmental samples by chiral liquid chromatography with tandem mass spectrometry.
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- Journal of Separation Science, 2018, v. 41, n. 6, p. 1287, doi. 10.1002/jssc.201701259
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Thermodynamic enantioseparation behavior of phenylthiohydantoin‐amino acid derivatives in supercritical fluid chromatography on polysaccharide chiral stationary phases.
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- Journal of Separation Science, 2018, v. 41, n. 6, p. 1450, doi. 10.1002/jssc.201701196
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Development of a capillary electrophoresis method for the determination of the chiral purity of dextromethorphan by a dual selector system using quality by design methodology.
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- Journal of Separation Science, 2018, v. 41, n. 6, p. 1405, doi. 10.1002/jssc.201701166
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Validation of warfarin enantiomer analysis method in plasma using high-performance liquid chromatography fluorescence detector.
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- Journal of Advanced Pharmaceutical Technology & Research, 2022, v. 13, n. 1, p. 18, doi. 10.4103/japtr.japtr_259_21
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Positron Annihilation Lifetime Analysis of Left- and Right-Handed Alanine Single Crystals.
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- Acta Physica Polonica: A, 2017, v. 132, n. 5, p. 1456, doi. 10.12693/APhysPolA.132.1456
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Synthesis and characterization of novel silica coated magnetic nanoparticles with tags of β-cyclodextrin: application as an eco-friendly and chiral micro-vessel catalyst in the enantioselective reduction of ketones.
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- Research on Chemical Intermediates, 2018, v. 44, n. 4, p. 2719, doi. 10.1007/s11164-018-3256-9
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Distinction of clenbuterol intake from drug or contaminated food of animal origin in a controlled administration trial – the potential of enantiomeric separation for doping control analysis.
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- Food Additives & Contaminants. Part A: Chemistry, Analysis, Control, Exposure & Risk Assessment, 2017, v. 34, n. 4, p. 525, doi. 10.1080/19440049.2016.1242169
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Mirror-Image Packing Provides a Molecular Basis for the Nanomolar Equipotency of Enantiomers of an Experimental Herbicide.
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- Angewandte Chemie, 2016, v. 128, n. 43, p. 13683, doi. 10.1002/ange.201607185
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Electrochemical recognition for tryptophan enantiomers based on 3, 4, 9, 10-perylenetetracarboxylic acid-chitosan composite film.
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- Journal of Solid State Electrochemistry, 2018, v. 22, n. 8, p. 2405, doi. 10.1007/s10008-018-3960-9
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Cu(I)-Catalyzed Asymmetric Cross-Coupling of N-Tosylhydrazones and Trialkylsilylethynes: Enantioselective Construction of C(sp)--C(sp³) Bonds.
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- Chinese Journal of Chemistry, 2018, v. 36, n. 3, p. 217, doi. 10.1002/cjoc.201700633
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Chiral analysis of E‐ε‐viniferin enantiomers, towards a new chemotaxonomic marker of the vine.
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- Journal of the Science of Food & Agriculture, 2023, v. 103, n. 5, p. 2295, doi. 10.1002/jsfa.12444
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Cage-Like B<sub>41</sub><sup>+</sup> and B<sub>42</sub><sup>2+</sup>: New Chiral Members of the Borospherene Family.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 28, p. 8160, doi. 10.1002/anie.201501588
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Total Synthesis and Biological Evaluation of the Antibiotic Lysocin E and Its Enantiomeric, Epimeric, and N-Demethylated Analogues.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 5, p. 1556, doi. 10.1002/anie.201410270
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Three-Dimensional Near-Surface Imaging of Chirality Domains with Circularly Polarized X-rays.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 33, p. 8718, doi. 10.1002/anie.201303023
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Fabrication of Chiral Stationary Phases via Continuous Assembly of Polymers for Resolution of Enantiomers by Liquid Chromatography.
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- Macromolecular Materials & Engineering, 2014, v. 299, n. 11, p. 1285, doi. 10.1002/mame.201400103
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A New Benzyl Phenethanolamine-b-Cyclodextrin Bonded Phase: Chiral Chromatography Performance and Application for LC-MS/MS Analysis of Pesticide Enantiomers in Fruits and Vegetables.
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- Journal of AOAC International, 2022, v. 105, n. 5, p. 1319, doi. 10.1093/jaoacint/qsac047
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Combination of the Suzuki–Miyaura Cross‐Coupling Reaction with Engineered Transaminases.
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- Chemistry - A European Journal, 2018, v. 24, n. 60, p. 16009, doi. 10.1002/chem.201804366
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Separation and analysis of nicotine enantiomers in tobacco and tobacco products using chiral column-HPLC-DAD method.
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- Journal of Light Industry, 2018, v. 33, n. 5, p. 44, doi. 10.3969/j.issn.2096-1553.2018.05.006
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Comparison of Enantiomeric Separations and Screening Protocols for Chiral Primary Amines by SFC and HPLC.
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- LC-GC Europe, 2015, v. 28, n. 1, p. 26
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Precise analysis of thyroxine enantiomers in pharmaceutical formulation by mobility difference based on cyclodextrin.
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- Arabian Journal of Chemistry, 2023, v. 16, n. 6, p. N.PAG, doi. 10.1016/j.arabjc.2023.104718
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Novel N-Doped Carbon Dots/β-Cyclodextrin Nanocomposites for Enantioselective Recognition of Tryptophan Enantiomers.
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- Sensors (14248220), 2016, v. 16, n. 11, p. 1874, doi. 10.3390/s16111874
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Cyclodextrin-based Gas Chromatography and GC/MS methods for determination of chiral pair constituents in mint essential oils.
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- Journal of Essential Oil Research, 2021, v. 33, n. 1, p. 23, doi. 10.1080/10412905.2020.1835744
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Non-Equimolar Discrete Phases Formed in the System of Malic Acid Enantiomers.
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- Chemical Engineering & Technology, 2015, v. 38, n. 6, p. 1047, doi. 10.1002/ceat.201400753
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Enantioselective Multidimensional Gas Chromatography for the Analysis of Selected Monoterpenic Compounds in Melaleuca alternifolia (Tea Tree) oil.
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- Reinvention: An International Journal of Undergraduate Research, 2015, v. 8, n. 2, p. 1
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Study on kinetics of reactive extraction of propranolol enantiomers by multiple linear regression method.
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- Asia-Pacific Journal of Chemical Engineering, 2017, v. 12, n. 4, p. 551, doi. 10.1002/apj.2097
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Chiral Teropyrenes: Synthesis, Structure, and Spectroscopic Studies.
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- Angewandte Chemie, 2024, v. 136, n. 33, p. 1, doi. 10.1002/ange.202404849
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Structure‐retention relationship for enantioseparation of selected fluoroquinolones.
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- Chirality, 2018, v. 30, n. 6, p. 828, doi. 10.1002/chir.22861
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Enantioselective resolution of <italic>Rac</italic>‐terbutaline and evaluation of optically pure <italic>R</italic>‐terbutaline hydrochloride as an efficient anti‐asthmatic drug.
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- Chirality, 2018, v. 30, n. 6, p. 759, doi. 10.1002/chir.22846
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Production of (R)‐1‐(1,3‐benzodioxol‐5‐yl)ethanol in high enantiomeric purity by Lactobacillus paracasei BD101.
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- Chirality, 2018, v. 30, n. 2, p. 189, doi. 10.1002/chir.22782
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Chiral exploration of 6,12-diphenyldibenzo[ b, f][1,5]diazocine with stable conformation.
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- Chirality, 2017, v. 29, n. 3/4, p. 134, doi. 10.1002/chir.22680
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Comparison of intestinal permeability and p-glycoprotein effects on the intestinal absorption of enantiomers of 2-(2-hydroxypropanamido) benzoic acid in rats.
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- Chirality, 2017, v. 29, n. 1, p. 26, doi. 10.1002/chir.22662
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Analysis of flumequine enantiomers in rat plasma by UFLC-ESI-MS/MS.
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- Chirality, 2016, v. 28, n. 11, p. 737, doi. 10.1002/chir.22654
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Cyclodextrin-Functionalized Monolithic Capillary Columns: Preparation and Chiral Applications.
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- Chirality, 2016, v. 28, n. 2, p. 97, doi. 10.1002/chir.22550
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Separation of Enantiomers by Inclusion.
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- Chirality, 2016, v. 28, n. 2, p. 124, doi. 10.1002/chir.22557
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Simultaneous Chiral Separation of Flavanone, Naringenin, and Hesperetin Enantiomers by RP-UHPLC-DAD.
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- Chirality, 2016, v. 28, n. 2, p. 147, doi. 10.1002/chir.22559
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Determination of Trantinterol Enantiomers in Human Plasma by High-Performance.
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- Chirality, 2015, v. 27, n. 5, p. 327, doi. 10.1002/chir.22432
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GC Separation of Enantiomers of Alkyl Esters of 2-Bromo Substituted.
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- Chirality, 2014, v. 26, n. 6, p. 279, doi. 10.1002/chir.22310
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Reviews.
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- Chirality, 2013, v. 25, n. 10, p. 622, doi. 10.1002/chir.22187
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