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Measurement of the Dimerization Equilibrium Constants of Enantiomers
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.198906261openalex-snapshot
Chromatographic Separation of the Excess Enantiomer under Achiral Conditions
inferredcites →https://doi.org/10.1007/978-3-030-84961-0openalex-snapshot
Stereochemistry of Organic Compounds
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Computer simulation of three scenarios for the separation of non-racemic mixtures by chromatography on achiral stationary phases
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Enantiomeric enrichment of partially resolved 4-hydroxy-2-carboxymethylcyclopentanone de derivatives by achiral phase chromatography
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Fourier transform pulsed-gradient spin-echo studies of molecular diffusion
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Deviations from Beer's law due to dimerization equilibria: theoretical comparison of absorbance, fluorescence and thermal lens measurements
inferredcites →https://doi.org/10.1016/s0021-9673(00)00486-6openalex-snapshot
On-line monitoring of enantiomer concentration in chiral simulated moving bed chromatography
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Separation of binaphthol enantiomers through achiral chromatography
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Unexpected pehnomenon in the high-performance liquid chromatographic anlaysis of racemic 14C-labelled nicotine: Separation of enantiomers in a totally achiral system
inferredcites →https://doi.org/10.1016/s0021-9673(98)00339-2openalex-snapshot
Enantiomeric enrichment of non-racemic antihistamines by achiral high-performance liquid chromatography
inferredcites →https://doi.org/10.1016/s0040-4020(01)97323-5openalex-snapshot
Interactions diastereoisomeres d'antipodes en phase liquide
inferredcites →https://doi.org/10.1021/ac00144a043openalex-snapshot
Self-induced chiral recognition in the association of enantiomeric mixtures on silica gel chromatography
inferredcites →https://doi.org/10.1021/j100099a048openalex-snapshot
Enantiomer Recognition of Asymmetric Catalysts. Thermodynamic Properties of Homochiral and Heterochiral Dimers of the Methylzinc Alkoxide Formed from Dimethylzinc and Enantiomeric 3-exo-(Dimethylamino)isoborneol
inferredcites →https://doi.org/10.1021/ja00269a036openalex-snapshot
Nonlinear effects in asymmetric synthesis. Examples in asymmetric oxidations and aldolization reactions
inferredcites →https://doi.org/10.1021/om000104iopenalex-snapshot
Applications of Pulsed Field Gradient Spin−Echo Measurements to the Determination of Molecular Diffusion (and Thus Size) in Organometallic Chemistry
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Specific Optical Rotations and the Horeau Effect
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The self‐disproportionation of enantiomers (SDE): The effect of scaling down, potential problems versus prospective applications, possible new occurrences, and unrealized opportunities?
inferred← citeshttps://doi.org/10.1002/hlca.200490172openalex-snapshot
Determination of the Dimerization Equilibrium Constants of Omeprazole and Pirkle's Alcohol through Optical‐Rotation Measurements
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Enantioseparations in Achiral Environments and Chromatographic Systems
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Probing interactions by means of pulsed field gradient nuclear magnetic resonance spectroscopy
inferred← citeshttps://doi.org/10.1007/128_2013_434openalex-snapshot
Self-disproportionation of Enantiomers of Enantiomerically Enriched Compounds
inferred← citeshttps://doi.org/10.1007/s11084-012-9265-6openalex-snapshot
Separation of Chiral Molecules: A Way to Homochirality
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Probing Interactions Between Small Molecules and Polymers by Means of NMR Spectroscopy
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General model for the achiral chromatography of enantiomers forming dimers: application to binaphthol
inferred← citeshttps://doi.org/10.1016/j.chroma.2006.02.001openalex-snapshot
Adsorption behavior of the ()-Tröger’s base enantiomers in the phase system of a silica-based packing coated with amylose tri(3,5-dimethyl carbamate) and 2-propanol and molecular modeling interpretation
inferred← citeshttps://doi.org/10.1016/j.chroma.2008.11.016openalex-snapshot
Elaborate treatment of retention in chemoselective chromatography—The retention increment approach and non-linear effects
inferred← citeshttps://doi.org/10.1016/j.chroma.2023.463877openalex-snapshot
Separation of non-racemic mixtures of enantiomers by achiral chromatography
inferred← citeshttps://doi.org/10.1016/j.chroma.2023.464603openalex-snapshot
Altering the mobile phase composition to enhance self-disproportionation of enantiomers in achiral chromatography
inferred← citeshttps://doi.org/10.1016/j.chroma.2025.466175openalex-snapshot
Effect of temperature on chromatographic separation driven by enantiomer self-disproportionation
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2009.12.002openalex-snapshot
Self-disproportionation of enantiomers of heterocyclic compounds having a tertiary trifluoromethyl alcohol center on chromatography with a non-chiral system
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2005.06.020openalex-snapshot
Chiral recognition and behavior of [1,1′-binaphthalene]-2,2′-diol in aqueous solution by fluorescence spectroscopy
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2008.06.021openalex-snapshot
Fluorescence properties of (R)- and (S)-[1,1′-binaphthalene]-2,2′-diols solutions and their complexes with cyclodextrins in aqueous medium
inferred← citeshttps://doi.org/10.1016/j.molstruc.2010.07.026openalex-snapshot
Structural characterization of racemic 1,1′-bi-(2-naphthol) monopivalate and its 6-nitro derivative
inferred← citeshttps://doi.org/10.1016/j.phytol.2017.09.017openalex-snapshot
Benzoate esters and flavonoids from Desmos pedunculosus
inferred← citeshttps://doi.org/10.1016/j.tetasy.2006.12.028openalex-snapshot
First catalytic enantioselective synthesis of the cocaine abuse therapeutic agent (S)-(+)-1-(4-{2-[bis(4-fluorophenyl)methoxy]ethyl}piperazin-1-yl)-2-phenyl-2-propanol
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.03.035openalex-snapshot
Enantiodifferentiation of phytoalexin spirobrassinin derivatives using the chiral solvating agent (R)-(+)-1,1′-bi-2-naphthol in conjunction with molecular modeling
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.04.027openalex-snapshot
Nonlinear effects in enantioselective chromatography: prediction of unusual elution profiles of enantiomers in non-racemic mixtures on an achiral stationary phase doped with small amounts of a chiral selector
inferred← citeshttps://doi.org/10.1016/j.trac.2018.07.020openalex-snapshot
Self-induced recognition of enantiomers (SIRE) and its application in chiral NMR analysis
inferred← citeshttps://doi.org/10.1016/s0021-9673(01)01366-8openalex-snapshot
Separation of binaphthol enantiomers through achiral chromatography
inferred← citeshttps://doi.org/10.1021/cg901219fopenalex-snapshot
The Origin of Life and the Crystallization of Aspartic Acid in Water
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Optical Rotation of Noncovalent Aggregates
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Thermo-/Mechano-Chromic Chiral Coordination Dimer: Formation of Switchable and Metastable Discrete Structure through Chiral Self-Sorting
inferred← citeshttps://doi.org/10.1021/jacs.5c01251openalex-snapshot
Toward Chiral Recognition by Design: Uncovering the Self-Enantioresolving Properties of Chiral Amine Derivatives
inferred← citeshttps://doi.org/10.1021/jacs.5c20238openalex-snapshot
Aromatic Interactions Select for Homodimeric Assembly in a Quadruply Hydrogen-Bonded DADA 1,2-Azaphosphinine Dimer
inferred← citeshttps://doi.org/10.1021/jp0721806openalex-snapshot
Specific Anion Effects on the Optical Rotation of α-Amino Acids
inferred← citeshttps://doi.org/10.1039/b607100gopenalex-snapshot
Experimental evidence for the homochiral aggregation of ammonium salts in solution
inferred← citeshttps://doi.org/10.1039/b814905dopenalex-snapshot
NMR and molecular modeling of the dimeric self-association of the enantiomers of 1,1′-bi-2-naphthol and 1-phenyl-2,2,2-trifluoroethanol in the solution state and their relevance to enantiomer self-disproportionation on achiral-phase chromatography (ESDAC)
inferred← citeshttps://doi.org/10.1039/c2cs35006hopenalex-snapshot
Self-disproportionation of enantiomers via achiral chromatography: a warning and an extra dimension in optical purifications
inferred← citeshttps://doi.org/10.1039/c5cp01834jopenalex-snapshot
Wavelength resolved specific optical rotations and homochiral equilibria
inferred← citeshttps://doi.org/10.1039/c6cp01247gopenalex-snapshot
Solvation dependence observed in the electronic dissymmetry factor spectra: how much information are we missing by analyzing the circular dichroism spectra alone?
inferred← citeshttps://doi.org/10.1039/c7sc05138gopenalex-snapshot
The self-disproportionation of enantiomers (SDE): a menace or an opportunity?
inferred← citeshttps://doi.org/10.1039/d0ob01497dopenalex-snapshot
Optical purity, enantiomeric excess and the Horeau effect
inferred← citeshttps://doi.org/10.1201/9781315374888-10openalex-snapshot
Chiral Aggregation, Equilibria, and the Horeau Effect
inferred← citeshttps://doi.org/10.3390/molecules26092757openalex-snapshot
Recommended Tests for the Self-Disproportionation of Enantiomers (SDE) to Ensure Accurate Reporting of the Stereochemical Outcome of Enantioselective Reactions
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