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Self-induced chiral recognition in the association of enantiomeric mixtures on silica gel chromatography

https://doi.org/10.1021/ac00144a043
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/bip.1976.360151015openalex-snapshot
Étude expérimentale de l'auto‐association des molécules modèles dipeptidiques. II. Association stéréosélective des molécules énantiomères
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Enantiomer‐Differentiation Induced by an Enantiomeric Excess during Chromatography with Achiral Phases
inferredcites →https://doi.org/10.1007/bf00492792openalex-snapshot
Separations on a mercuric-acetate-substituted phenylsilica phase in normal-phase liquid chromatography
inferredcites →https://doi.org/10.1016/0016-2361(86)90019-0openalex-snapshot
Isolation of sulphur heterocycles from petroleum- and coal-derived materials by ligand exchange chromatography
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Sulphur heterocycles in coal-derived products
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An NMR study of optical isomers in solution
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Comparison of acitvity coefficients measured by a static and by a dynamic method
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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(01)92750-5openalex-snapshot
Self-amplification of optical activity by chromatography on an achiral adsorbent
inferredcites →https://doi.org/10.1021/ac00124a029openalex-snapshot
Supercritical fluid fractionation and detailed characterization of the sulfur heterocycles in a catalytically cracked petroleum vacuum residue
inferredcites →https://doi.org/10.1021/ja00262a027openalex-snapshot
Self-induced nonequivalence in the association of D- and L-amino acid derivatives
inferredcites →https://doi.org/10.1021/ja00338a042openalex-snapshot
Conformational study of N-acyl amino acid esters and thiol esters by FT-IR and x-ray crystallography: evidence for a nitrogen...sulfur interaction in thiol esters
inferredcites →https://doi.org/10.1021/ja00357a047openalex-snapshot
Hydrogen bonding in optically active and racemic 2-butanol
inferredcites →https://doi.org/10.1021/ma60053a022openalex-snapshot
Polydepsipeptides. 5. Experimental Conformational Analysis of Poly(L-alanyl-L-lactic acid) and Related Model Compounds

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Enantiomeric enrichment of non-racemic mixtures of binaphthol with non-chiral packings
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Nichtlineare Effekte bei asymmetrischen Synthesen und stereoselektiven Reaktionen
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Die chromatographische Abtrennung des überschüssigen Enantiomers unter achiralen Bedingungen
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Remarkable Amplification of the Self‐Disproportionation of Enantiomers on Achiral‐Phase Chromatography Columns
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Chromatographic Separation of the Excess Enantiomer under Achiral Conditions
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Remarkable Amplification of the Self‐Disproportionation of Enantiomers on Achiral‐Phase Chromatography Columns
inferred← citeshttps://doi.org/10.1002/bmc.502openalex-snapshot
Enantiorecognition on solid chiral selectors using microbatch technology: an example of limitation in case of strong association in the racemate
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Possible Case of Halogen Bond‐Driven Self‐Disproportionation of Enantiomers (SDE) via Achiral Chromatography
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Experimental studies of competition between enantiomers in chiral liquid chromatography through their system peaks
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Determination of the Dimerization Equilibrium Constants of Omeprazole and Pirkle's Alcohol through Optical‐Rotation Measurements
inferred← citeshttps://doi.org/10.1002/hlca.201300392openalex-snapshot
Purification of Enantiomeric Mixtures in Enantioselective Synthesis: Overlooked Errors and Scientific Basis of Separation in Achiral Environment
inferred← citeshttps://doi.org/10.1002/ijch.201600077openalex-snapshot
Self‐disproportionation of Enantiomers (SDE) of Chiral Nonracemic Amides via Achiral Chromatography
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Enantioseparations in Achiral Environments and Chromatographic Systems
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Self-disproportionation of Enantiomers of Enantiomerically Enriched Compounds
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Chiroptical Detectors for the Study of Unusual Phenomena in Chiral Chromatography
inferred← citeshttps://doi.org/10.1007/978-1-4613-0699-3_12openalex-snapshot
Other direct chiral resolution methods
inferred← citeshttps://doi.org/10.1007/978-94-009-0861-1_12openalex-snapshot
Other direct chiral resolution methods
inferred← citeshttps://doi.org/10.1007/bf02272816openalex-snapshot
Effect of solute association on the apparent adsorption isotherm. A model of the separation of non-racemic mixtures of enantiomers in achiral chromatographic systems
inferred← citeshttps://doi.org/10.1007/s00726-019-02729-yopenalex-snapshot
The self-disproportionation of enantiomers (SDE) of amino acids and their derivatives
inferred← citeshttps://doi.org/10.1016/0016-2361(93)90301-hopenalex-snapshot
Isolation of aliphatic sulfur compounds in a crude oil by a non-reactive procedure
inferred← citeshttps://doi.org/10.1016/0021-9673(94)80413-3openalex-snapshot
Resolution of non-racemic mixtures in achiral chromatographic systems: A model for, the enantioselective effects observed
inferred← citeshttps://doi.org/10.1016/0021-9673(95)00385-zopenalex-snapshot
Enantiomeric enrichment of partially resolved 4-hydroxy-2-carboxymethylcyclopentanone de derivatives by achiral phase chromatography
inferred← citeshttps://doi.org/10.1016/b978-0-08-044860-2.00002-7openalex-snapshot
Practical Aspects of Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1016/b978-0-12-812958-6.00010-0openalex-snapshot
Fluorine-Containing Pharmaceuticals and the Phenomenon of the Self-Disproportionation of Enantiomers
inferred← citeshttps://doi.org/10.1016/j.chroma.2003.10.071openalex-snapshot
General model for the achiral chromatography of enantiomers forming dimers: application to binaphthol
inferred← citeshttps://doi.org/10.1016/j.chroma.2006.08.059openalex-snapshot
Chromatographic elution profile of an analyte involved in reversible chemical reaction of the type A+B↔AB
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.2023.464603openalex-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.chroma.2025.466608openalex-snapshot
Equilibrium theory-based framework for descripting separation of enantiomers by frontal achiral chromatography
inferred← citeshttps://doi.org/10.1016/j.chroma.2026.467101openalex-snapshot
Effect of modification of silica surface on the extent of enantiomer self-disproportionation
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2005.11.004openalex-snapshot
Self-disproportionation of enantiomers of (R)-ethyl 3-(3,5-dinitrobenzamido)-4,4,4-trifluorobutanoate on achiral silica gel stationary phase
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.tet.2009.10.095openalex-snapshot
Atropisomeric lactam chemistry: catalytic enantioselective synthesis, application to asymmetric enolate chemistry and synthesis of key intermediates for NET inhibitors
inferred← citeshttps://doi.org/10.1016/j.tet.2012.03.054openalex-snapshot
Self-disproportionation of enantiomers of non-racemic chiral amine derivatives through achiral chromatography
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.tetasy.2010.04.040openalex-snapshot
Rational application of self-disproportionation of enantiomers via sublimation—a novel methodological dimension for enantiomeric purifications
inferred← citeshttps://doi.org/10.1016/j.tetasy.2012.11.004openalex-snapshot
Catalytic enantioselective synthesis of atropisomeric 2-aryl-4-quinolinone derivatives with an N–C chiral axis
inferred← citeshttps://doi.org/10.1016/j.tetasy.2016.03.004openalex-snapshot
Chiral additive induced self-disproportionation of enantiomers under MPLC conditions: preparation of enantiomerically pure samples of 1-(aryl)ethylamines from racemates
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.07.061openalex-snapshot
Chiral initiator-induces self-disproportionation of enantiomers via achiral chromatography: application to enantiomer separation of racemate
inferred← citeshttps://doi.org/10.1016/s0021-9673(01)01366-8openalex-snapshot
Separation of binaphthol enantiomers through achiral chromatography
inferred← citeshttps://doi.org/10.1016/s0021-9673(98)00339-2openalex-snapshot
Enantiomeric enrichment of non-racemic antihistamines by achiral high-performance liquid chromatography
inferred← citeshttps://doi.org/10.1016/s1460-1567(96)80024-9openalex-snapshot
Chapter 2 Analytical methods
inferred← citeshttps://doi.org/10.1021/acs.analchem.2c01212openalex-snapshot
Exploiting Self-Association to Evaluate Enantiomeric Composition by Cyclic Ion Mobility–Mass Spectrometry
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Mass Spectrometric Characterization of Organosulfur Compounds Using Palladium(II) as a Sensitivity-Enhancing Reagent
inferred← citeshttps://doi.org/10.1021/ef990207hopenalex-snapshot
Isolation and Characterization of the Saturate and Aromatic Fractions of a Maya Crude Oil
inferred← citeshttps://doi.org/10.1021/jo0155052openalex-snapshot
Synthesis, Absolute Configuration, and Enantiomeric Enrichment of a Cruciferous Oxindole Phytoalexin, (S)-(−)-Spirobrassinin, and Its Oxazoline Analog
inferred← citeshttps://doi.org/10.1021/jo971995fopenalex-snapshot
Symmetry-Assisted Synthesis of C2-Symmetric trans-α,α‘-Bis(hydroxymethyl)pyrrolidine and -piperidine Derivatives via Double Sharpless Asymmetric Dihydroxylation of α,ω-Terminal Dienes
inferred← citeshttps://doi.org/10.1021/jp020352nopenalex-snapshot
Measurement of the Dimerization Equilibrium Constants of Enantiomers
inferred← citeshttps://doi.org/10.1021/np000043topenalex-snapshot
Enantiomeric Excess of a Cruciferous Phytoalexin, Spirobrassinin, and Its Enantiomeric Enrichment in an Achiral HPLC System
inferred← citeshttps://doi.org/10.1039/a704779gopenalex-snapshot
A study of asymmetric protonation with chiral β-hydroxy sulfoxides. Asymmetric synthesis of (–)-epibatidine
inferred← citeshttps://doi.org/10.1039/a707196eopenalex-snapshot
Synthesis, enzymic resolution and enantiomeric enhancement of bis(hydroxymethyl)[7]thiaheterohelicenes
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/c5ra01496dopenalex-snapshot
Resolution of enantiomers with both achiral phases in chromatography: conceptual challenge
inferred← citeshttps://doi.org/10.1039/c6cs00703aopenalex-snapshot
Chiral sulfoxides: advances in asymmetric synthesis and problems with the accurate determination of the stereochemical outcome
inferred← citeshttps://doi.org/10.1039/c7sc05138gopenalex-snapshot
The self-disproportionation of enantiomers (SDE): a menace or an opportunity?
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Self-disproportionation of enantiomers (SDE) of chiral sulfur-containing compounds via achiral chromatography
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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A General Phenomenon of Spontaneous Amplification of Optical Purity under Achiral Chromatographic Conditions
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