Works matching DE "ENANTIOMERS"
Results: 3251
Synthesis and Applications of Functionalized Magnetic Nanomaterials in Enantioseparation.
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- Separation & Purification Reviews, 2019, v. 48, n. 1, p. 14, doi. 10.1080/15422119.2017.1419257
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Part III: Supercritical Fluid Chromatographic Separations.
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- Separation & Purification Reviews, 2008, v. 37, n. 3, p. 229, doi. 10.1080/15422110701873098
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Part II: From Dermatologicals to Sensory Organ and Various Drugs.
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- Separation & Purification Reviews, 2008, v. 37, n. 1/2, p. 1, doi. 10.1080/15422110701873007
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Commercial Chiral Stationary Phases for the Separations of Clinical Racemic Drugs.
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- Separation & Purification Reviews, 2007, v. 36, n. 4, p. 285, doi. 10.1080/15422110701826997
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Inhibitory Effect of Mispyric Acid on Mammalian DNA Polymerases.
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- Bioscience, Biotechnology & Biochemistry, 2005, v. 69, n. 8, p. 1534, doi. 10.1271/bbb.69.1534
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Formation of trans-Verbenol and Verbenone from α-Pinene Catalysed by Immobilised Picea abies Cells.
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- Bioscience, Biotechnology & Biochemistry, 2005, v. 69, n. 2, p. 321, doi. 10.1271/bbb.69.321
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Synthesis, Absolute Configuration and Biological Activities of Both Enantiomers of 2-(5,7-Dichloro-3-indolyl)propionic Acid: a Novel Dichloroindole Auxin and Antiauxin.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 6, p. 1287, doi. 10.1271/bbb.68.1287
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Niotransformation of &alpha-Isomethylionone to 1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)propan-2-one.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 5, p. 1164, doi. 10.1271/bbb.68.1164
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Synthesis of All Four Stereoisomers of 3-Amino-2-hydroxybutanoic Acids.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 3, p. 714, doi. 10.1271/bbb.68.714
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Chiral Discrimination of Branched-chain Fatty Acids by Reversed-phase HPLC after Labeling with a Chiral Fluorescent Conversation Reagent.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 1, p. 153, doi. 10.1271/bbb.68.153
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Synthetic Racemate and Enantiomers of Cytosporone E, a Metabolite of an Endophytic Fungus, Show Indistinguishably Weak Antimicrobial Activity.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 12, p. 2584, doi. 10.1271/bbb.67.2584
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Synthesis and Absolute Configuration of (-)-3-Butyl-7-hydroxyphthalide, a Cytotoxic Metabolite of Penicillium vulpinum.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 10, p. 2240, doi. 10.1271/bbb.67.2240
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Synthesis of the Enantiomers of 21-Methyl-7-hentriacontanone and a Stereoisomeric Mixture of 5-Acetoxy-19-methylnonacosane, Candidates for the Female Sex Pheromone of the Screwworm Fly, Cochliomyia hominivorax.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 10, p. 2224, doi. 10.1271/bbb.67.2224
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Synthesis of the Racemate and Both Enantiomers of Massoilactone.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 10, p. 2210, doi. 10.1271/bbb.67.2210
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Systematic Strategy for the Synthesis of Cyanobacterin and Its Stereoisomers. 1. Asymmetric Total Synthesis of Dechloro-cyanobacterin and Its Enantiomer.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 10, p. 2183, doi. 10.1271/bbb.67.2183
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New Method for Synthesizing the Intermediates to 5-HETE from Yeast-mediated Reduction Products by Employing Baeyer-Villiger Oxidation with Complete Retention of Enantiomeric Excess.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 9, p. 1959, doi. 10.1271/bbb.67.1959
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Asymmetric Chloronicotinyl Insecticide, 1-[1-(6-Chloro-3-pyridyl)ethyl]-2-nitroiminoimidazolidine: Preparation, Resolution and Biological Activities toward Insects and Their Nerve Preparations.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 5, p. 980, doi. 10.1271/bbb.67.980
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Unique Transitions in Morphology and Characteristics of Porous Poly(Lactic Acid) Enantiomers.
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- Macromolecular Chemistry & Physics, 2018, v. 219, n. 7, p. 1, doi. 10.1002/macp.201700547
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Central-to-Axial Chirality Transfer-Induced CD Sensor for Chiral Recognition and ee Value Detection of 1,2-DACH Enantiomers.
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- Macromolecular Chemistry & Physics, 2015, v. 216, n. 19, p. 1925, doi. 10.1002/macp.201500236
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AIE‐Active Circularly Polarized Thermally Activated Delayed Fluorescence Emitters for Stable Solution‐Processed Circularly Polarized Electroluminescence.
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- Chemistry - A European Journal, 2025, v. 31, n. 15, p. 1, doi. 10.1002/chem.202403970
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D‐π‐A Type [7]Helicene‐like Imide Derivatives with Tunable Photophysical Properties and Circularly Polarized Luminescence.
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- Chemistry - A European Journal, 2024, v. 30, n. 71, p. 1, doi. 10.1002/chem.202403292
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Twist along Central C−C Bonds in a Series of Fully π‐Fused Propellanes.
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- Chemistry - A European Journal, 2024, v. 30, n. 68, p. 1, doi. 10.1002/chem.202402828
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Synthesis Strategies, Preparation Methods, and Applications of Chiral Metal‐Organic Frameworks.
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- Chemistry - A European Journal, 2024, v. 30, n. 34, p. 1, doi. 10.1002/chem.202401091
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Structure and Chiroptical Properties of Anthra[1,2‐a]anthracene‐1‐yl Dimers as New Biaryls.
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- Chemistry - A European Journal, 2024, v. 30, n. 31, p. 1, doi. 10.1002/chem.202400929
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Construction and Application of a Pepsin‐Functionalized Covalent Organic Framework with Prominent Chiral Recognition Ability.
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- Chemistry - A European Journal, 2024, v. 30, n. 15, p. 1, doi. 10.1002/chem.202303827
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Total Chemical Synthesis of the SARS‐CoV‐2 Spike Receptor‐Binding Domain.
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- Chemistry - A European Journal, 2024, v. 30, n. 3, p. 1, doi. 10.1002/chem.202302969
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Asymmetric Transfer Hydrogenation as a Key Step in the Synthesis of the Phosphonic Acid Analogs of Aminocarboxylic Acids.
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- Chemistry - A European Journal, 2023, v. 29, n. 72, p. 1, doi. 10.1002/chem.202302171
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Front Cover: Chiral‐at‐Metal Racemization Unraveled for MX<sub>2</sub>(a‐chel)<sub>2</sub> by means of a Computational Analysis of MoO<sub>2</sub>(acnac)<sub>2</sub> (Chem. Eur. J. 66/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 66, p. 1, doi. 10.1002/chem.202303604
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One‐Pot Synthesis of Helical Azaheptalene and Chiroptical Switching of an Isolable Radical Cation**.
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- Chemistry - A European Journal, 2023, v. 29, n. 48, p. 1, doi. 10.1002/chem.202301759
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Crystallographic Deciphering of Spontaneous Self‐Assembly of Achiral Calciphores to Chiral Complexes.
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- Chemistry - A European Journal, 2023, v. 29, n. 10, p. 1, doi. 10.1002/chem.202203127
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Enantiomeric Resolution and Enantiomer Isolation of H<sub>2</sub>TPPS4 J‐Aggregate from Aqueous Solution Is Enabled by Vortexes.
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- Chemistry - A European Journal, 2023, v. 29, n. 7, p. 1, doi. 10.1002/chem.202202337
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Design and Synthesis of a Ferrocene‐Based Diol Library and Application in the Hetero‐Diels‐Alder Reaction.
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- Chemistry - A European Journal, 2023, v. 29, n. 6, p. 1, doi. 10.1002/chem.202203006
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Bright Organic Mechanoluminescence and Remarkable Mechanofluorochromism from Circularly Polarized TADF Enantiomers with Aggregation‐Induced Emission Properties**.
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- Chemistry - A European Journal, 2023, v. 29, n. 5, p. 1, doi. 10.1002/chem.202202594
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Synthesis of Isomeric Tb<sup>3+</sup>‐Phthalocyanine Double‐Decker Complexes Depending on the Difference in the Direction of Coordination Plane and Their Magnetic Properties.
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- Chemistry - A European Journal, 2023, v. 29, n. 1, p. 1, doi. 10.1002/chem.202203272
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Chiral‐at‐Metal Silver‐Mediated Base Pairs: Metal‐Centred Chirality versus DNA Helical Chirality.
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- Chemistry - A European Journal, 2023, v. 29, n. 3, p. 1, doi. 10.1002/chem.202202630
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YfeX – A New Platform for Carbene Transferase Development with High Intrinsic Reactivity.
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- Chemistry - A European Journal, 2022, v. 28, n. 65, p. 1, doi. 10.1002/chem.202201474
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Brønsted Acid versus Phase‐Transfer Catalysis in the Enantioselective Transannular Aminohalogenation of Enesultams.
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- Chemistry - A European Journal, 2022, v. 28, n. 62, p. 1, doi. 10.1002/chem.202202267
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Enantiomer‐Selective Molecular Sensing in the Nonlinear Optical Regime via Upconverting Chiral Metamaterials.
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- Advanced Functional Materials, 2022, v. 32, n. 43, p. 1, doi. 10.1002/adfm.202208641
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Chirality‐Based Biosensors.
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- Advanced Functional Materials, 2019, v. 29, n. 1, p. N.PAG, doi. 10.1002/adfm.201805512
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Chiral discrimination of enantiomers based on different interactions with alterable chiral oligomer.
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- Journal of Polymer Research, 2021, v. 28, n. 12, p. 1, doi. 10.1007/s10965-021-02832-3
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Multiple melting behavior of poly(epichlorohydrin) enantiomorphs.
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- Journal of Materials Science, 1999, v. 34, n. 6, p. 1323, doi. 10.1023/A:1004502232614
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Distinct binding of cetirizine enantiomers to human serum albumin and the human histamine receptor H<sub>1</sub>.
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- Journal of Computer-Aided Molecular Design, 2020, v. 34, n. 10, p. 1045, doi. 10.1007/s10822-020-00328-8
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Significantly different effects of tetrahydroberberrubine enantiomers on dopamine D1/D2 receptors revealed by experimental study and integrated in silico simulation.
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- Journal of Computer-Aided Molecular Design, 2019, v. 33, n. 4, p. 447, doi. 10.1007/s10822-019-00194-z
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pK based protonation states and microspecies for protein-ligand docking.
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- Journal of Computer-Aided Molecular Design, 2010, v. 24, n. 11, p. 935, doi. 10.1007/s10822-010-9385-x
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ElectroShape: fast molecular similarity calculations incorporating shape, chirality and electrostatics.
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- Journal of Computer-Aided Molecular Design, 2010, v. 24, n. 9, p. 789, doi. 10.1007/s10822-010-9374-0
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Enantioselectivity of mass spectrometry: Challenges and promises.
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- Mass Spectrometry Reviews, 2013, v. 32, n. 6, p. 466, doi. 10.1002/mas.21379
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Amino Acids in Life: A Prebiotic Division of Labor.
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- Journal of Molecular Evolution, 2019, v. 87, n. 1, p. 1, doi. 10.1007/s00239-018-9879-z
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Rationale and conditions for the requirement of chiral bioanalytical methods in bioequivalence studies.
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- European Journal of Clinical Pharmacology, 2010, v. 66, n. 6, p. 599, doi. 10.1007/s00228-010-0792-7
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Estimation of the area under the concentration-time curve of racemic lansoprazole by using limited plasma concentration of lansoprazole enantiomers.
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- European Journal of Clinical Pharmacology, 2008, v. 64, n. 5, p. 503, doi. 10.1007/s00228-007-0455-5
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Inhibition of CYP3A4 and CYP3A5 catalyzed metabolism of alprazolam and quinine by ketoconazole as racemate and four different enantiomers.
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- European Journal of Clinical Pharmacology, 2007, v. 63, n. 2, p. 173, doi. 10.1007/s00228-006-0230-z
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