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S(+)-ketamine.
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- Wiener Klinische Wochenschrift, 2018, v. 130, n. 9/10, p. 356, doi. 10.1007/s00508-017-1299-3
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Application of the method of projective representations to the analysis of exciton-phonon transitions in enantiomorphous tetragonal crystals ZnP<sub>2</sub> and CdP<sub>2</sub>.
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- Semiconductor Physics, Quantum Electronics & Optoelectronics, 2005, v. 8, n. 1, p. 19, doi. 10.15407/spqeo8.01.019
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Determination of Concentration of Methotrexate Enantiomers in Intracellular and Extracellular Fluids of HepG<sub>2</sub> Cells by Liquid Chromatography–Tandem Mass Spectrometry.
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- Cell Biochemistry & Biophysics, 2013, v. 67, n. 3, p. 1343, doi. 10.1007/s12013-013-9666-9
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Synthesis of both enantiomers of lycoperdic acid, an unusual mushroom-derived amino acid.
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- Bioscience, Biotechnology & Biochemistry, 2021, v. 85, n. 1, p. 154, doi. 10.1093/bbb/zbaa027
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Synthesis of (12R,13S)-pyriculariol and (12R,13S)-dihydropyriculariol revealed that the rice blast fungus, Pyricularia oryzae, produces these phytotoxins as racemates.
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- Bioscience, Biotechnology & Biochemistry, 2021, v. 85, n. 1, p. 134, doi. 10.1093/bbb/zbaa002
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Asymmetric synthesis of trans-p-menth-3-ene-1,2,8-triol, the monoterpene isolated from herbal plants.
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- Bioscience, Biotechnology & Biochemistry, 2020, v. 84, n. 1, p. 37, doi. 10.1080/09168451.2019.1671789
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Enantiospecific synthesis and filed evaluation of four stereoisomers of 10,14-dimethyloctadec-l-ene, a sex pheromone component secreted by female moths of the apple leafminer.
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- Bioscience, Biotechnology & Biochemistry, 2014, v. 78, n. 5, p. 761, doi. 10.1080/09168451.2014.905187
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Stereoselective peptide analysis.
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- Analytical & Bioanalytical Chemistry, 2005, v. 382, n. 3, p. 599, doi. 10.1007/s00216-005-3091-x
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Ultrasonic extraction followed by sulfuric acid silica gel cleanup for the determination of a-hexachlorocyclohexane enantiomers in biota samples.
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- Analytical & Bioanalytical Chemistry, 2005, v. 381, n. 6, p. 1248, doi. 10.1007/s00216-004-3041-z
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- Article
Enantiomer discrimination by mass spectrometry: noncovalent interactions of an N-derivatized dipeptide with various cinchona alkaloid derivatives and comparison with enantioselective liquid-phase separations.
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- Analytical & Bioanalytical Chemistry, 2004, v. 379, n. 7/8, p. 1039, doi. 10.1007/s00216-004-2689-8
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Liquid chromatographic method for the determination of enantiomeric composition of amphetamine and methamphetamine in hair samples.
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- Analytical & Bioanalytical Chemistry, 2004, v. 378, n. 1, p. 144, doi. 10.1007/s00216-003-2366-3
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Separation of the enantiomers of substituted dihydrofurocoumarins by HPLC using macrocyclic glycopeptide chiral stationary phases.
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- Analytical & Bioanalytical Chemistry, 2003, v. 377, n. 4, p. 639, doi. 10.1007/s00216-003-2110-z
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Quantitative enantiomeric analysis of chlorcyclizine, hydroxyzine, and meclizine by capillary electrophoresis.
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- Analytical & Bioanalytical Chemistry, 2003, v. 376, n. 6, p. 859, doi. 10.1007/s00216-003-2015-x
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Separation of positional isomers by the use of coupled shape-selective stationary phase columns.
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- Analytical & Bioanalytical Chemistry, 2003, v. 375, n. 5, p. 635, doi. 10.1007/s00216-003-1768-6
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Chiral Recognition of Tryptophan Enantiomers Based on β-Cyclodextrin-platinum Nanoparticles/Graphene Nanohybrids Modified Electrode.
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- Electroanalysis, 2016, v. 28, n. 4, p. 868, doi. 10.1002/elan.201500548
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Enantioselective Recognition of DOPA by Mesoporous Platinum Imprinted with Mandelic Acid.
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- Electroanalysis, 2015, v. 27, n. 9, p. 2209, doi. 10.1002/elan.201500145
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Chiral Recognition of Proline Enantiomers by the Catalytic Oxygen Reduction and Formation of Cu(II)-Polymer Complex Crystals.
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- Electroanalysis, 2014, v. 26, n. 10, p. 2110, doi. 10.1002/elan.201400405
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Exploiting Ternary Solubility Phase Diagrams for Resolution of Enantiomers: An Instructive Example.
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- Chemical Engineering & Technology, 2020, v. 43, n. 2, p. 329, doi. 10.1002/ceat.201900421
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Towards Diastereomeric Pure Salts with Antisolvent Methods.
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- Chemical Engineering & Technology, 2018, v. 41, n. 7, p. 1466, doi. 10.1002/ceat.201700429
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Particle Size Distributions and Performance of Preferential Crystallization of L‐Asparagine·H<sub>2</sub>O with Tailor‐Made Additives.
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- Chemical Engineering & Technology, 2018, v. 41, n. 6, p. 1173, doi. 10.1002/ceat.201700668
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Advanced Operating Strategies to Extend the Applications of Simulated Moving Bed Chromatography.
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- Chemical Engineering & Technology, 2017, v. 40, n. 12, p. 2163, doi. 10.1002/ceat.201700206
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Model of Temperature Cycle-Induced Deracemization via Differences in Crystal Growth Rate Dispersion.
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- Chemical Engineering & Technology, 2017, v. 40, n. 7, p. 1252, doi. 10.1002/ceat.201600746
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Stereoselective Crystallization as a Basis for Single-Enantiomer Drug Production.
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- Chemical Engineering & Technology, 2017, v. 40, n. 7, p. 1211, doi. 10.1002/ceat.201600649
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Stereoselective Behavior of Nafion® Membranes towards (+)- α-Pinene and (−)- α-Pinene.
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- Chemical Engineering & Technology, 2015, v. 38, n. 9, p. 1617, doi. 10.1002/ceat.201400621
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Mathematical Modeling of Chiral Symmetry Breaking due to Differences in Crystal Growth Kinetics.
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- Chemical Engineering & Technology, 2014, v. 37, n. 8, p. 1329, doi. 10.1002/ceat.201400056
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Coupled Continuous Chromatography and Racemization Processes for the Production of Pure Enantiomers.
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- Chemical Engineering & Technology, 2014, v. 37, n. 4, p. 643, doi. 10.1002/ceat.201300597
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Dynamics and Control of Coupled Continuous Chromatography and Crystallization Processes for the Production of Pure Enantiomers.
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- Chemical Engineering & Technology, 2013, v. 36, n. 8, p. 1417, doi. 10.1002/ceat.201200279
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Zwei Diterpensynthasen aus Chryseobacterium: Chryseodien‐Synthase und Wanjudien‐Synthase.
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- Angewandte Chemie, 2020, v. 132, n. 29, p. 12041, doi. 10.1002/ange.202004691
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Enantiocomplementary Epoxidation Reactions Catalyzed by an Engineered Cofactor‐Independent Non‐natural Peroxygenase.
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- Angewandte Chemie, 2020, v. 132, n. 26, p. 10460, doi. 10.1002/ange.202001373
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Synthesis of Both Enantiomers of Nine‐Membered CF<sub>3</sub>‐Substituted Heterocycles Using a Single Chiral Ligand: Palladium‐Catalyzed Decarboxylative Ring Expansion with Kinetic Resolution.
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- Angewandte Chemie, 2020, v. 132, n. 21, p. 8264, doi. 10.1002/ange.201915021
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Carbene‐Catalyzed Dynamic Kinetic Resolution and Asymmetric Acylation of Hydroxyphthalides and Related Natural Products.
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- Angewandte Chemie, 2020, v. 132, n. 10, p. 3887, doi. 10.1002/ange.201912926
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Axially Chiral TADF‐Active Enantiomers Designed for Efficient Blue Circularly Polarized Electroluminescence.
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- Angewandte Chemie, 2020, v. 132, n. 9, p. 3528, doi. 10.1002/ange.201914249
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Enantiomorphic Microvortex‐Enabled Supramolecular Sensing of Racemic Amino Acids by Using Achiral Building Blocks.
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- Angewandte Chemie, 2020, v. 132, n. 9, p. 3514, doi. 10.1002/ange.201913882
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Metastable Chiral Azobenzenes Stabilized in a Double Racemate.
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- Angewandte Chemie, 2020, v. 132, n. 8, p. 3227, doi. 10.1002/ange.201910687
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Organic Room‐Temperature Phosphorescence with Strong Circularly Polarized Luminescence Based on Paracyclophanes.
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- Angewandte Chemie, 2019, v. 131, n. 48, p. 17380, doi. 10.1002/ange.201909076
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Innentitelbild: Enantiospecific Desorption Triggered by Circularly Polarized Light (Angew. Chem. 44/2019).
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- Angewandte Chemie, 2019, v. 131, n. 44, p. 15702, doi. 10.1002/ange.201912595
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Enantiospecific Desorption Triggered by Circularly Polarized Light.
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- Angewandte Chemie, 2019, v. 131, n. 44, p. 15832, doi. 10.1002/ange.201906630
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Enantioselective Dicarbofunctionalization of Unactivated Alkenes by Palladium‐Catalyzed Tandem Heck/Suzuki Coupling Reaction.
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- Angewandte Chemie, 2019, v. 131, n. 41, p. 14795, doi. 10.1002/ange.201907840
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Stereochemical Dichotomy in Two Competing Cascade Processes: Total Syntheses of Both Enantiomers of Spiroxin A.
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- Angewandte Chemie, 2019, v. 131, n. 36, p. 12637, doi. 10.1002/ange.201906762
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Rhodium‐Catalyzed Parallel Kinetic Resolution of Racemic Internal Allenes Towards Enantiopure Allylic 1,3‐Diketones.
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- Angewandte Chemie, 2019, v. 131, n. 29, p. 10044, doi. 10.1002/ange.201903365
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Interplay of H‐Bonds with Aromatics in Isolated Complexes Identifies Isomeric Carbohydrates.
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- Angewandte Chemie, 2019, v. 131, n. 22, p. 7424, doi. 10.1002/ange.201902377
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Spontaneous Resolution by Crystallization of an Octanuclear Iron(III) Complex Using Only Racemic Reagents.
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- Angewandte Chemie, 2019, v. 131, n. 22, p. 7402, doi. 10.1002/ange.201901877
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Potential‐Induced Fine‐Tuning of the Enantioaffinity of Chiral Metal Phases.
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- Angewandte Chemie, 2019, v. 131, n. 11, p. 3509, doi. 10.1002/ange.201900408
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Design and Catalytic Asymmetric Construction of Axially Chiral 3,3′‐Bisindole Skeletons.
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- Angewandte Chemie, 2019, v. 131, n. 10, p. 3046, doi. 10.1002/ange.201981061
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Enantioselective Electrophilic Aromatic Nitration: A Chiral Auxiliary Approach.
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- Angewandte Chemie, 2019, v. 131, n. 4, p. 1047, doi. 10.1002/ange.201811517
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Catalytic Enantioselective α‐Ketol Rearrangement.
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- Angewandte Chemie, 2019, v. 131, n. 2, p. 509, doi. 10.1002/ange.201812244
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Nanographene Imides Featuring Dual‐Core Sixfold [5]Helicenes.
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- Angewandte Chemie, 2019, v. 131, n. 1, p. 184, doi. 10.1002/ange.201810734
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Incorporation of Homochirality into a Zeolitic Imidazolate Framework Membrane for Efficient Chiral Separation.
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- Angewandte Chemie, 2018, v. 130, n. 52, p. 17376, doi. 10.1002/ange.201810925
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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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Solid‐Phase Conversion of Four Stereoisomers into a Single Enantiomer.
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- Angewandte Chemie, 2018, v. 130, n. 47, p. 15667, doi. 10.1002/ange.201808913
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