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https://doi.org/10.2139/ssrn.4594473
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Enantiomeric enrichment of non-racemic mixtures of binaphthol with non-chiral packings
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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
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Enantiomer self‐disproportionation of chiral compounds on achiral ordered mesoporous silica M41S and regular silica gel as a stationary phase
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Optical Purifications via Self‐Disproportionation of Enantiomers by Achiral Chromatography: Case Study of a Series of α‐CF3‐containing Secondary Alcohols
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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?
inferredcites →https://doi.org/10.1002/hlca.19850680818openalex-extracted
Enantiomer‐Differentiation Induced by an Enantiomeric Excess during Chromatography with Achiral Phases
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Determination of the Dimerization Equilibrium Constants of Omeprazole and Pirkle's Alcohol through Optical‐Rotation Measurements
inferredcites →https://doi.org/10.1002/hlca.201500041openalex-extracted
Enantiomeric Enrichments via the Self‐Disproportionation of Enantiomers (SDE) by Achiral, Gravity‐Driven Column Chromatography: a Case Study Using N‐(1‐Phenylethyl)acetamide for Optimizing the Enantiomerically Pure Yield and Magnitude of the SDE
inferredcites →https://doi.org/10.1007/bf02272816openalex-extracted
Effect of solute association on the apparent adsorption isotherm. A model of the separation of non-racemic mixtures of enantiomers in achiral chromatographic systems
inferredcites →https://doi.org/10.1007/s00726-015-2152-5openalex-extracted
Remarkable magnitude of the self-disproportionation of enantiomers (SDE) via achiral chromatography: application to the practical-scale enantiopurification of β-amino acid esters
inferredcites →https://doi.org/10.1007/s00726-018-2664-xopenalex-extracted
The self-disproportionation of enantiomers (SDE) of α-amino acid derivatives: facets of steric and electronic properties
inferredcites →https://doi.org/10.1007/s00726-019-02774-7openalex-extracted
The self-disproportionation of enantiomers (SDE) via column chromatography of β-amino-α,α-difluorophosphonic acid derivatives
inferredcites →https://doi.org/10.1016/0021-9673(92)85233-jopenalex-extracted
Computer simulation of three scenarios for the separation of non-racemic mixtures by chromatography on achiral stationary phases
inferredcites →https://doi.org/10.1016/0021-9673(95)00385-zopenalex-extracted
Enantiomeric enrichment of partially resolved 4-hydroxy-2-carboxymethylcyclopentanone de derivatives by achiral phase chromatography
inferredcites →https://doi.org/10.1016/j.chroma.2003.10.071openalex-extracted
General model for the achiral chromatography of enantiomers forming dimers: application to binaphthol
inferredcites →https://doi.org/10.1016/j.chroma.2023.463877openalex-extracted
Separation of non-racemic mixtures of enantiomers by achiral chromatography
inferredcites →https://doi.org/10.1016/j.cis.2010.12.007openalex-extracted
Understanding protein adsorption phenomena at solid surfaces
inferredcites →https://doi.org/10.1016/j.tet.2012.03.054openalex-extracted
Self-disproportionation of enantiomers of non-racemic chiral amine derivatives through achiral chromatography
inferredcites →https://doi.org/10.1016/j.tet.2018.01.006openalex-extracted
Access to the enantiopure pyrrolobenzodiazepine (PBD) dilactam nucleus via self-disproportionation of enantiomers
inferredcites →https://doi.org/10.1016/j.tetasy.2010.04.040openalex-extracted
Rational application of self-disproportionation of enantiomers via sublimation—a novel methodological dimension for enantiomeric purifications
inferredcites →https://doi.org/10.1016/j.tetasy.2013.06.008openalex-extracted
Self-disproportionation of enantiomers of prazoles via achiral, gravity-driven silica gel column chromatography
inferredcites →https://doi.org/10.1016/j.tetasy.2016.03.004openalex-extracted
Chiral additive induced self-disproportionation of enantiomers under MPLC conditions: preparation of enantiomerically pure samples of 1-(aryl)ethylamines from racemates
inferredcites →https://doi.org/10.1016/j.tetlet.2013.07.061openalex-extracted
Chiral initiator-induces self-disproportionation of enantiomers via achiral chromatography: application to enantiomer separation of racemate
inferredcites →https://doi.org/10.1016/s0006-3495(01)76136-xopenalex-extracted
Effects of Excluded Surface Area and Adsorbate Clustering on Surface Adsorption of Proteins. II. Kinetic Models
inferredcites →https://doi.org/10.1016/s0021-9673(01)01366-8openalex-extracted
Separation of binaphthol enantiomers through achiral chromatography
inferredcites →https://doi.org/10.1016/s0021-9673(01)92750-5openalex-extracted
Self-amplification of optical activity by chromatography on an achiral adsorbent
inferredcites →https://doi.org/10.1021/ac00144a043openalex-extracted
Self-induced chiral recognition in the association of enantiomeric mixtures on silica gel chromatography
inferredcites →https://doi.org/10.1021/acs.jpcc.6b07758openalex-extracted
Competing Forces in Chiral Surface Chemistry: Enantiospecificity versus Enantiomer Aggregation
inferredcites →https://doi.org/10.1021/ja065603aopenalex-extracted
Phenomenon of Optical Self-Purification of Chiral Non-Racemic Compounds
inferredcites →https://doi.org/10.1021/jo00081a015openalex-extracted
Enantiomeric enrichment of sulfoxides by preparative flash chromatography on an achiral phase
inferredcites →https://doi.org/10.1021/jp020352nopenalex-extracted
Measurement of the Dimerization Equilibrium Constants of Enantiomers
inferredcites →https://doi.org/10.1038/nchem.2250openalex-extracted
Adsorption-induced auto-amplification of enantiomeric excess on an achiral surface
inferredcites →https://doi.org/10.1038/s41598-018-35457-6openalex-extracted
Understanding the Thalidomide Chirality in Biological Processes by the Self-disproportionation of Enantiomers
inferredcites →https://doi.org/10.1039/c2cc37491aopenalex-extracted
Unconventional preparation of racemic crystals of isopropyl 3,3,3-trifluoro-2-hydroxypropanoate and their unusual crystallographic structure: the ultimate preference for homochiral intermolecular interactions
inferredcites →https://doi.org/10.1039/c2cs35006hopenalex-extracted
Self-disproportionation of enantiomers via achiral chromatography: a warning and an extra dimension in optical purifications
inferredcites →https://doi.org/10.1039/c4ra13928copenalex-extracted
A comprehensive examination of the self-disproportionation of enantiomers (SDE) of chiral amides via achiral, laboratory-routine, gravity-driven column chromatography
inferredcites →https://doi.org/10.1039/c4sc03047hopenalex-extracted
Self-disproportionation of enantiomers of thalidomide and its fluorinated analogue via gravity-driven achiral chromatography: mechanistic rationale and implications
inferredcites →https://doi.org/10.1039/c5ra01496dopenalex-extracted
Resolution of enantiomers with both achiral phases in chromatography: conceptual challenge
inferredcites →https://doi.org/10.1039/c6cs00703aopenalex-extracted
Chiral sulfoxides: advances in asymmetric synthesis and problems with the accurate determination of the stereochemical outcome
inferredcites →https://doi.org/10.1039/c7sc05138gopenalex-extracted
The self-disproportionation of enantiomers (SDE): a menace or an opportunity?
inferredcites →https://doi.org/10.1055/s-0032-1316812openalex-extracted
Self-Disproportionation of Enantiomers of Chiral, Non-Racemic Fluoroorganic Compounds: Role of Fluorine as Enabling Element
inferredcites →https://doi.org/10.2174/157017911794697303openalex-extracted
Self-Disproportionation of Enantiomers via Sublimation; New and Truly Green Dimension in Optical Purification
inferredcites →https://doi.org/10.3390/molecules26092757openalex-extracted
Recommended Tests for the Self-Disproportionation of Enantiomers (SDE) to Ensure Accurate Reporting of the Stereochemical Outcome of Enantioselective Reactions
inferredcites →https://doi.org/10.3390/separations10070382openalex-extracted
The Self-Disproportionation of Enantiomers (SDE) of α-Pinene via Evaporation off Silica Gel and Foam Fractionation—Validation of the Plausibility of SDE via Gas Chromatography (GC) for α-Pinene
inferredcites →https://doi.org/10.3390/sym12071106openalex-extracted
Potentially Mistaking Enantiomers for Different Compounds Due to the Self-Induced Diastereomeric Anisochronism (SIDA) Phenomenon
inferredcites →https://doi.org/10.3390/sym13040543openalex-extracted
Flurbiprofen: A Study of the Behavior of the Scalemate by Chromatography, Sublimation, and NMR
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