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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- Article
Works matching DE "CHIRAL recognition"
Results: 424
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Development of Low‐Molecular‐Weight Organogelators from Cyclic β‐Amino Acid: Effect of Stereochemistry and their Application on Visual Chiral Recognition of Amines.
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- Chemistry - A European Journal, 2023, v. 29, n. 11, p. 1, doi. 10.1002/chem.202202692
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- Article
3
A Pseudorotaxane System Containing γ‐Cyclodextrin Formed via Chiral Recognition with an Au<sup>I</sup><sub>6</sub>Ag<sup>I</sup><sub>3</sub>Cu<sup>II</sup><sub>3</sub> Molecular Cap.
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- Chemistry - A European Journal, 2021, v. 27, n. 64, p. 15981, doi. 10.1002/chem.202102769
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- Article
4
A Chiral Molecular Cage Comprising Diethynylallenes and N‐Heterotriangulenes for Enantioselective Recognition.
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- Chemistry - A European Journal, 2021, v. 27, n. 53, p. 13352, doi. 10.1002/chem.202101801
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5
Enantioselective Recognition of Racemic Amino Alcohols in Aqueous Solution by Chiral Metal‐Oxide Keplerate {Mo<sub>132</sub>} Cluster Capsules.
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- Chemistry - A European Journal, 2021, v. 27, n. 48, p. 12327, doi. 10.1002/chem.202100899
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- Article
6
Selection of Planar Chiral Conformations between Pillar[5,6]arenes Induced by Amino Acid Derivatives in Aqueous Media.
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- Chemistry - A European Journal, 2021, v. 27, n. 19, p. 5890, doi. 10.1002/chem.202004003
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7
Neutral Chiral Tetrakis‐Iodo‐Triazole Halogen‐Bond Donor for Chiral Recognition and Enantioselective Catalysis.
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- Chemistry - A European Journal, 2021, v. 27, n. 7, p. 2315, doi. 10.1002/chem.202005016
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8
Frontispiece: Through the Looking Glass: Chiral Recognition of Substrates and Products at the Active Sites of Racemases and Epimerases.
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- Chemistry - A European Journal, 2020, v. 26, n. 46, p. 1, doi. 10.1002/chem.202084661
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9
Through the Looking Glass: Chiral Recognition of Substrates and Products at the Active Sites of Racemases and Epimerases.
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- Chemistry - A European Journal, 2020, v. 26, n. 46, p. 10367, doi. 10.1002/chem.201905826
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- Article
10
Ring‐Opened Hemiporphyrazines: Helical Molecules Exhibiting Circularly Polarized Luminescence.
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- Chemistry - A European Journal, 2020, v. 26, n. 8, p. 1768, doi. 10.1002/chem.201905246
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- Article
11
Dynamic Inversion of Stereoselective Phosphate Binding to a Bisurea Receptor Controlled by Light and Heat.
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- Angewandte Chemie, 2016, v. 128, n. 3, p. 1013, doi. 10.1002/ange.201509479
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- Article
12
Photonic Patterns Printed in Chiral Nematic Mesoporous Resins.
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- Angewandte Chemie, 2015, v. 127, n. 14, p. 4378, doi. 10.1002/ange.201410411
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- Article
13
Synthesis of Bulky Cellulose Derivatives for Efficient Enantioselective Fluorescent Sensing.
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- Cellulose, 2024, v. 31, n. 9, p. 5779, doi. 10.1007/s10570-024-05959-w
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- Article
14
Synthesis by carbonate aminolysis and chiral recognition ability of cellulose 2,3-bis(3,5-dimethylphenyl carbamate)-6-(α-phenylethyl carbamate) selectors.
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- Cellulose, 2023, v. 30, n. 1, p. 153, doi. 10.1007/s10570-022-04898-8
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- Article
15
Enantioselective permeations of amino acids through L-proline-modified gold nanochannel membrane: an experimental and theoretical study.
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- Amino Acids, 2018, v. 50, n. 11, p. 1549, doi. 10.1007/s00726-018-2629-0
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16
Research Progress on the Development and Application of Cyclodextrin-Based Chromatographic Stationary Phases.
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- Separations (2297-8739), 2025, v. 12, n. 4, p. 97, doi. 10.3390/separations12040097
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- Article
17
Determination of Enantiomer in Tofacitinib Citrate Using Reversed-Phase Chiral High-Performance Liquid Chromatography.
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- Separations (2297-8739), 2024, v. 11, n. 3, p. 89, doi. 10.3390/separations11030089
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- Article
18
An Evaluation of Immobilized Poly-(S)- N -(1-phenylethyl)acrylamide Chiral Stationary Phases.
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- Separations (2297-8739), 2023, v. 10, n. 1, p. 11, doi. 10.3390/separations10010011
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19
Receptor Neuron Discrimination of the Germacrene D Enantiomers in the Moth Helicoverpa armigera.
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- Chemical Senses, 2002, v. 27, n. 2, p. 143, doi. 10.1093/chemse/27.2.143
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- Article
20
Corylus avellana L. Natural Signature: Chiral Recognition of Selected Informative Components in the Volatilome of High-Quality Hazelnuts.
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- Frontiers in Plant Science, 2022, v. 13, p. 1, doi. 10.3389/fpls.2022.844711
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- Article
21
Identifying Chirality in Line Drawings of Molecules Using Imbalanced Dataset Sampler for a Multilabel Classification Task.
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- Molecular Informatics, 2022, v. 41, n. 12, p. 1, doi. 10.1002/minf.202200068
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22
Organocatalyst Efficiency in the α-Aminoxylation and α-Hydrazination of Carbonyl Derivatives in Aqueous Media or in a Ball-Mill.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 8, p. 1191, doi. 10.1002/ejoc.201601357
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23
Recognition of PSL(2,2a) by the orders of vanishing elements.
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- Proceedings of the Indian Academy of Sciences: Mathematical Sciences, 2018, v. 128, n. 5, p. 1, doi. 10.1007/s12044-018-0435-y
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- Article
24
Frontispiece: The Hydrogen Bond and Beyond: Perspectives for Rotational Investigations of Non‐Covalent Interactions.
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- Chemistry - A European Journal, 2019, v. 25, n. 49, p. N.PAG, doi. 10.1002/chem.201984961
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25
The Hydrogen Bond and Beyond: Perspectives for Rotational Investigations of Non‐Covalent Interactions.
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- Chemistry - A European Journal, 2019, v. 25, n. 49, p. 11402, doi. 10.1002/chem.201901113
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- Article
26
Chiral Discrimination through <sup>1</sup>H NMR and Luminescence Spectroscopy: Dynamic Processes and Solid Strip for Chiral Recognition.
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- Chemistry - A European Journal, 2017, v. 23, n. 72, p. 18303, doi. 10.1002/chem.201704837
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27
Stereoselective Arene-Forming Aldol Condensation: Catalyst-Controlled Synthesis of Axially Chiral Compounds.
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- Chemistry - A European Journal, 2017, v. 23, n. 53, p. 12960, doi. 10.1002/chem.201702471
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28
Zinc-Coordinated Hierarchical Organization of Ligand-Stabilized Gold Nanoclusters for Chiral Recognition and Separation.
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- Chemistry - A European Journal, 2017, v. 23, n. 38, p. 9137, doi. 10.1002/chem.201701128
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29
C<sub>3</sub>-Symmetric Boron Lewis Acid with a Cage-Shape for Chiral Molecular Recognition and Asymmetric Catalysis.
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- Chemistry - A European Journal, 2017, v. 23, n. 6, p. 1273, doi. 10.1002/chem.201605712
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30
Anion Recognition by Aliphatic Helical Oligoureas.
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- Chemistry - A European Journal, 2016, v. 22, n. 44, p. 15549, doi. 10.1002/chem.201604240
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- Article
31
Biomimetic Taste Receptors with Chiral Recognition by Photoluminescent Metal-Organic Frameworks Chelated with Polyaniline Helices.
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- Chemistry - A European Journal, 2016, v. 22, n. 4, p. 1406, doi. 10.1002/chem.201503931
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32
Exploration of the Chiral Recognition of Sugar-Based Diindolylmethane Receptors: Anion and Receptor Structures.
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- Chemistry - A European Journal, 2015, v. 21, n. 46, p. 16585, doi. 10.1002/chem.201502932
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33
Helical Channel Mesoporous Materials with Embedded Magnetic Iron Nanoparticles: Chiral Recognition and Implications in Asymmetric Olefin Epoxidation.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 14/15, p. 3127, doi. 10.1002/adsc.201500441
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34
Chiral PDTDH-based electrode modification material for L/D-tartaric acid electrochemical sensing.
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- Journal of Polymer Research, 2020, v. 27, n. 8, p. N.PAG, doi. 10.1007/s10965-020-02181-7
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- Article
35
Kinetic and thermodynamic studies of molecularly imprinted polymers for the selective adsorption and specific enantiomeric recognition of D-mandelic acid.
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- Journal of Polymer Research, 2019, v. 26, n. 4, p. N.PAG, doi. 10.1007/s10965-019-1746-0
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- Article
36
Electrochemical Recognition of Phenylalanine Enantiomers Based on Silver Nanoparticles Modified Aminated Carbon Nanotubes.
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- Chirality, 2025, v. 37, n. 3, p. 1, doi. 10.1002/chir.70029
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37
Development of Acid‐Functionalized Molecularly Imprinted Phenolic Resin for Chiral Recognition of S‐Venlafaxine.
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- Chirality, 2025, v. 37, n. 3, p. 1, doi. 10.1002/chir.70023
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- Article
38
Voltammetric Sensor for Naproxen Enantiomers Based on a Paste Electrode Modified With a Chiral Nickel(II) Complex.
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- Chirality, 2025, v. 37, n. 2, p. 1, doi. 10.1002/chir.70025
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39
Chiral Differentiation of Chiral Lactides and Chiral Diketones on Native and Phenylcarbamoylated Cyclodextrin Chiral Stationary Phases.
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- Chirality, 2024, v. 36, n. 12, p. 1, doi. 10.1002/chir.70007
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40
Chiral Self‐Sorting Process With C<sub>2</sub> Symmetric Bisimidazoline Ligands.
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- Chirality, 2024, v. 36, n. 10, p. 1, doi. 10.1002/chir.23720
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41
Inherently Chiral Oligomers Based on Indole–Benzothiophene Core.
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- Chirality, 2024, v. 36, n. 8, p. 1, doi. 10.1002/chir.23710
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42
Enantiomeric Analysis of Chiral Drugs Using Mass Spectrometric Methods: A Comprehensive Review.
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- Chirality, 2024, v. 36, n. 8, p. 1, doi. 10.1002/chir.23705
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43
The Development of One New Normal Phase Liquid Chromatography Method and Thermodynamic Investigation of Olodaterol Hydrochloride Enantiomer.
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- Chirality, 2024, v. 36, n. 8, p. 1, doi. 10.1002/chir.23704
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- Article
44
Tandem Mass Spectrometry Approaches for Differentiation and Quantification Pidotimod and Its Three Isomers in the Gas Phase.
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- Chirality, 2024, v. 36, n. 8, p. 1, doi. 10.1002/chir.23699
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45
Preparation of amino acid chiral ionic liquid and visual chiral recognition of glutamine and phenylalanine enantiomers.
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- Chirality, 2024, v. 36, n. 4, p. 1, doi. 10.1002/chir.23665
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46
Chiral recognition and discrimination studies of tyrosine enantiomers on (−)‐18‐crown‐6‐tetracarboxylic acid as a chiral selector by nuclear magnetic resonance spectroscopy and docking simulations.
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- Chirality, 2024, v. 36, n. 3, p. 1, doi. 10.1002/chir.23656
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47
Enantiomeric separation of thiourea derivatives of naringenin on amylose and cellulose polymeric chromatographic chiral columns.
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- Chirality, 2024, v. 36, n. 3, p. 1, doi. 10.1002/chir.23659
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48
Enantioselective adsorption of ibuprofen enantiomers using chiral‐active carbon nanoparticles induced S‐α‐methylbenzylamine.
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- Chirality, 2024, v. 36, n. 1, p. 1, doi. 10.1002/chir.23628
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49
Chiral recognition mechanism studies of Tyr‐Arg‐Phe‐Lys‐NH<sub>2</sub> tetrapeptide on crown ether‐based chiral stationary phase.
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- Chirality, 2024, v. 36, n. 1, p. 1, doi. 10.1002/chir.23619
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50
Straightforward synthesis of chiral sulfonate‐based ionic liquids from amino alcohols for chiral recognition.
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- Chirality, 2023, v. 35, n. 12, p. 993, doi. 10.1002/chir.23614
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- Article