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Self-disproportionation of enantiomers of thalidomide and its fluorinated analogue via gravity-driven achiral chromatography: mechanistic rationale and implications
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1520-636x(1996)8:5<390::aid-chir6>3.0.co;2-iopenalex-snapshot
Enantioselective inhibition of TNF-? release by thalidomide and thalidomide-analogues
inferredcites →https://doi.org/10.1002/ange.19800920105openalex-snapshot
Chromatographische Racemattrennung
inferredcites →https://doi.org/10.1002/ange.200503373openalex-snapshot
Remarkable Amplification of the Self‐Disproportionation of Enantiomers on Achiral‐Phase Chromatography Columns
inferredcites →https://doi.org/10.1002/anie.200503373openalex-snapshot
Remarkable Amplification of the Self‐Disproportionation of Enantiomers on Achiral‐Phase Chromatography Columns
inferredcites →https://doi.org/10.1002/ardp.200700217openalex-snapshot
Thalidomide as a Multi‐Template for Development of Biologically Active Compounds
inferredcites →https://doi.org/10.1002/chir.20525openalex-snapshot
Enantiomer self‐disproportionation of chiral compounds on achiral ordered mesoporous silica M41S and regular silica gel as a stationary phase
inferredcites →https://doi.org/10.1002/chir.20917openalex-snapshot
Enantiomer self‐disproportionation and chiral stationary phase based selective chiral separation of organic compounds
inferredcites →https://doi.org/10.1002/chir.22180openalex-snapshot
Optical Purifications via Self‐Disproportionation of Enantiomers by Achiral Chromatography: Case Study of a Series of α‐CF3‐containing Secondary Alcohols
inferredcites →https://doi.org/10.1002/chir.530070109openalex-snapshot
Stereospecific determination, chiral inversion in vitro and pharmacokinetics in humans of the enantiomers of thalidomide
inferredcites →https://doi.org/10.1002/hlca.201300392openalex-snapshot
Purification of Enantiomeric Mixtures in Enantioselective Synthesis: Overlooked Errors and Scientific Basis of Separation in Achiral Environment
inferredcites →https://doi.org/10.1002/tera.1420380307openalex-snapshot
Proposed mechanisms of action in thalidomide embryopathy
inferredcites →https://doi.org/10.1007/128_2013_434openalex-snapshot
Self-disproportionation of Enantiomers of Enantiomerically Enriched Compounds
inferredcites →https://doi.org/10.1007/s002280100320openalex-snapshot
Clinical pharmacology of thalidomide
inferredcites →https://doi.org/10.1007/s11084-013-9333-6openalex-snapshot
Deracemization of Amino Acids by Partial Sublimation and via Homochiral Self-Organization
inferredcites →https://doi.org/10.1016/0021-9673(94)80385-4openalex-snapshot
Investigations on the in vitro racemization of thalidomide by high-performance liquid chromatography
inferredcites →https://doi.org/10.1016/0040-4020(96)00741-7openalex-snapshot
Asymmetric aldol reactions of trifluoromethyl ketones with a chiral Ni(II) complex of glycine: Stereocontrolling effect of the trifluoromethyl group
inferredcites →https://doi.org/10.1016/0957-4166(96)00177-2openalex-snapshot
Highly diastereoselective asymmetric aldol reactions of chiral Ni(II)-complex of glycine with alkyl trifluoromethyl ketones
inferredcites →https://doi.org/10.1016/j.bmcl.2009.02.108openalex-snapshot
Synthesis, configurational stability and stereochemical biological evaluations of (S)- and (R)-5-hydroxythalidomides
inferredcites →https://doi.org/10.1016/j.ejca.2004.07.023openalex-snapshot
Thalidomide in solid tumours: the resurrection of an old drug
inferredcites →https://doi.org/10.1016/j.ejps.2003.11.012openalex-snapshot
Hydrogen bond and other descriptors for thalidomide and its N-alkyl analogs; prediction of physicochemical and biological properties
inferredcites →https://doi.org/10.1016/j.ijpharm.2008.12.034openalex-snapshot
Solid state evaluation of some thalidomide raw materials
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.jfluchem.2009.10.002openalex-snapshot
Self-disproportionation of enantiomers of 3,3,3-trifluorolactic acid amides via sublimation
inferredcites →https://doi.org/10.1016/j.jfluchem.2009.10.018openalex-snapshot
NMR spectral enantioresolution of spirobrassinin and 1-methoxyspirobrassinin enantiomers using (S)-(−)-ethyl lactate and modeling of spirobrassinin self-association for rationalization of its self-induced diastereomeric anisochromism (SIDA) and enantiomer self-disproportionation on achiral-phase…
inferredcites →https://doi.org/10.1016/j.jfluchem.2009.11.010openalex-snapshot
Self-disproportionation of enantiomers of α-trifluoromethyl lactic acid amides via sublimation
inferredcites →https://doi.org/10.1016/j.jfluchem.2009.11.015openalex-snapshot
Chirality-dependent sublimation of -(trifluoromethyl)-lactic acid: Relative vapor pressures of racemic, eutectic, and enantiomerically pure forms, and vibrational spectroscopy of isolated (S,S) and (S,R) dimers
inferredcites →https://doi.org/10.1016/j.jfluchem.2009.11.026openalex-snapshot
Self-disproportionation of enantiomers of isopropyl 3,3,3-(trifluoro)lactate via sublimation: Sublimation rates vs. enantiomeric composition
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.jfluchem.2009.12.007openalex-snapshot
Discrimination of enantiomeric excess of optically active trifluorolactate by distillation: Evidence for a multi-center hydrogen bonding network in the liquid state
inferredcites →https://doi.org/10.1016/j.jfluchem.2009.12.008openalex-snapshot
Attempts to explain the self-disproportionation observed in the partial sublimation of enantiomerically enriched carboxylic acids
inferredcites →https://doi.org/10.1016/j.jfluchem.2009.12.018openalex-snapshot
First principle lattice energy calculations for enantiopure and racemic crystals of α-(trifluoromethyl)lactic acid: Is self-disproportionation of enantiomers controlled by thermodynamic stability of crystals?
inferredcites →https://doi.org/10.1016/j.molstruc.2006.11.039openalex-snapshot
Calorimetric determinations and theoretical calculations of polymorphs of thalidomide
inferredcites →https://doi.org/10.1016/j.tet.2012.03.054openalex-snapshot
Self-disproportionation of enantiomers of non-racemic chiral amine derivatives through achiral chromatography
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.tetasy.2013.06.008openalex-snapshot
Self-disproportionation of enantiomers of prazoles via achiral, gravity-driven silica gel column chromatography
inferredcites →https://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
inferredcites →https://doi.org/10.1016/s0040-4039(00)79964-3openalex-snapshot
Highly diastereoselective aldol reaction of fluoroalkyl aryl ketones with methyl isocyanoacetate catalyzed by silver(I)/triethylamine
inferredcites →https://doi.org/10.1016/s0140-6736(62)91217-5openalex-snapshot
THALIDOMIDE AND CONGENITAL ABNORMALITIES
inferredcites →https://doi.org/10.1016/s0149-2918(03)80085-1openalex-snapshot
Thalidomide: A review of approved and investigational uses
inferredcites →https://doi.org/10.1021/ja065603aopenalex-snapshot
Phenomenon of Optical Self-Purification of Chiral Non-Racemic Compounds
inferredcites →https://doi.org/10.1021/jo4017474openalex-snapshot
Partial Sublimation of Enantioenriched Amino Acids at Low Temperature. Is it Coming From the Formation of a Euatmotic Composition1 of the Gaseous Phase?
inferredcites →https://doi.org/10.1021/jo9623402openalex-snapshot
Transition Metal/Base-Catalyzed Aldol Reactions of Isocyanoacetic Acid Derivatives with Prochiral Ketones, a Straightforward Approach to Stereochemically Defined β,β-Disubstituted-β-hydroxy-α-amino Acids.1 Scope and Limitations
inferredcites →https://doi.org/10.1021/ol102818gopenalex-snapshot
Asymmetric Synthesis of Both Mirror Images of 3′-Fluorothalidomide by Enantiodivergent Fluorination Using a Single, Cinchona Alkaloid
inferredcites →https://doi.org/10.1021/ol9902172openalex-snapshot
(R)- and (S)-3-Fluorothalidomides: Isosteric Analogues of Thalidomide
inferredcites →https://doi.org/10.1021/tx200005gopenalex-snapshot
In Vivo Formation of a Glutathione Conjugate Derived from Thalidomide in Humanized uPA-NOG Mice
inferredcites →https://doi.org/10.1021/tx300009jopenalex-snapshot
In Vivo Formation of Dihydroxylated and Glutathione Conjugate Metabolites Derived from Thalidomide and 5-Hydroxythalidomide in Humanized TK-NOG Mice
inferredcites →https://doi.org/10.1021/tx400008gopenalex-snapshot
In Vivo Drug Interactions of the Teratogen Thalidomide with Midazolam: Heterotropic Cooperativity of Human Cytochrome P450 in Humanized TK-NOG Mice
inferredcites →https://doi.org/10.1021/tx4004215openalex-snapshot
Human Cytochrome P450 Oxidation of 5-Hydroxythalidomide and Pomalidomide, an Amino Analogue of Thalidomide
inferredcites →https://doi.org/10.1021/tx4004374openalex-snapshot
Thalidomide Increases Human Hepatic Cytochrome P450 3A Enzymes by Direct Activation of the Pregnane X Receptor
inferredcites →https://doi.org/10.1021/tx900367popenalex-snapshot
Human Liver Microsomal Cytochrome P450 3A Enzymes Involved in Thalidomide 5-Hydroxylation and Formation of a Glutathione Conjugate
inferredcites →https://doi.org/10.1038/215296a0openalex-snapshot
Toxicity and Teratogenicity of Optical Isomers of Thalidomide
inferredcites →https://doi.org/10.1038/nrc1323openalex-snapshot
The evolution of thalidomide and its IMiD derivatives as anticancer agents
inferredcites →https://doi.org/10.1039/b616196kopenalex-snapshot
Serine sublimes with spontaneous chiral amplification
inferredcites →https://doi.org/10.1039/b702882bopenalex-snapshot
An astrophysically-relevant mechanism for amino acid enantiomer enrichment
inferredcites →https://doi.org/10.1039/b711844aopenalex-snapshot
Understanding organofluorine chemistry. An introduction to the C–F bond
inferredcites →https://doi.org/10.1039/b802459fopenalex-snapshot
Enzymatic resolution and evaluation of enantiomers of cis-5′-hydroxythalidomide
inferredcites →https://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)
inferredcites →https://doi.org/10.1039/c0cc04271dopenalex-snapshot
Asymmetric amplification in amino acidsublimation involving racemic compound to conglomerate conversion
inferredcites →https://doi.org/10.1039/c0cp01155jopenalex-snapshot
Theoretical investigations into the enantiomeric and racemic forms of α-(trifluoromethyl)lactic acid
inferredcites →https://doi.org/10.1039/c2cc37491aopenalex-snapshot
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-snapshot
Self-disproportionation of enantiomers via achiral chromatography: a warning and an extra dimension in optical purifications
inferredcites →https://doi.org/10.1039/c4ob00831fopenalex-snapshot
The self-disproportionation of the enantiomers (SDE) of methyl n-pentyl sulfoxide via achiral, gravity-driven column chromatography: a case study
inferredcites →https://doi.org/10.1039/j29710001073openalex-snapshot
Crystal and molecular structure of thalidomide, N-(α-glutarimido)-phthalimide
inferredcites →https://doi.org/10.1039/p19930003143openalex-snapshot
General method for the synthesis of enantiomerically pure β-hydroxy-α-amino acids, containing fluorine atoms in the side chains. Case of stereochemical distinction between methyl and trifluoromethyl groups. X-Ray crystal and molecular structure of the nickel( II ) complex of…
inferredcites →https://doi.org/10.1039/p29940002063openalex-snapshot
Characterization and crystal structure of two polymorphic forms of racemic thalidomide
inferredcites →https://doi.org/10.1055/s-0032-1316812openalex-snapshot
Self-Disproportionation of Enantiomers of Chiral, Non-Racemic Fluoroorganic Compounds: Role of Fluorine as Enabling Element
inferredcites →https://doi.org/10.1080/01411591003605986openalex-snapshot
Evaluation of stability difference between asymmetric homochiral dimer in (S)-thalidomide crystal and symmetric heterochiral dimer in (RS)-thalidomide crystal
inferredcites →https://doi.org/10.1093/toxsci/kfr086openalex-snapshot
Fluorothalidomide: A Characterization of Maternal and Developmental Toxicity in Rabbits and Mice
inferredcites →https://doi.org/10.1111/j.1365-2133.2005.06747.xopenalex-snapshot
Thalidomide: dermatological indications, mechanisms of action and side-effects
inferredcites →https://doi.org/10.1126/science.154.3754.1362-bopenalex-snapshot
Response : Thalidomide Solutions
inferredcites →https://doi.org/10.1200/jco.2004.10.127openalex-snapshot
Thalidomide: Current Role in the Treatment of Non-Plasma Cell Malignancies
inferredcites →https://doi.org/10.1246/cl.1996.115openalex-snapshot
Separation of an Enantiomorph and Its Racemate by Distillation: Strong Chiral Recognizing Ability of Trifluorolactates
inferredcites →https://doi.org/10.1246/cl.2009.1046openalex-snapshot
Design and Synthesis of Thalidomide–Deoxyribonucleoside Chimeras
inferredcites →https://doi.org/10.1248/cpb.42.1157openalex-snapshot
(S)-Form of .ALPHA.-Methyl-N(.ALPHA.)-phthalimidoglutarimide, but Not Its (R)-Form, Enhanced Phorbol Ester-Induced Tumor Necrosis Factor-.ALPHA. Production by Human Leukemia Cell HL-60: Implication of Optical Resolution of Thalidomidal Effects.
inferredcites →https://doi.org/10.1248/cpb.58.110openalex-snapshot
Synthesis and Configurational Stability of (S)- and (R)-Deuteriothalidomides
inferredcites →https://doi.org/10.1358/dof.2004.029.04.792298openalex-snapshot
Thalidomide as a multitarget drug and its application as a template for drug design
inferredcites →https://doi.org/10.1517/13543776.14.2.215openalex-snapshot
Thalidomide analogues: derivatives of an orphan drug with diverse biological activity
inferredcites →https://doi.org/10.2174/157017911794697303openalex-snapshot
Self-Disproportionation of Enantiomers via Sublimation; New and Truly Green Dimension in Optical Purification
inferredcites →https://doi.org/10.3762/bjoc.6.38openalex-snapshot
The C–F bond as a conformational tool in organic and biological chemistry
inferredcites →https://doi.org/10.3816/cgc.2004.n.014openalex-snapshot
Thalidomide and Analogues: Current Proposed Mechanisms and Therapeutic Usage
inferredcites →https://doi.org/10.4161/cc.7.9.5793openalex-snapshot
Shedding light on an old mystery: Thalidomide suppresses survival pathways to induce limb defects
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9783527825158.ch9openalex-snapshot
The Self‐Disproportionation of Enantiomers ( SDE ): Fluorine as an SDE ‐Phoric Substituent
inferred← citeshttps://doi.org/10.1002/adsc.202101369openalex-snapshot
Mechanistic Insights into Annulation of Arylidene‐Δ2‐Pyrrolin‐4‐Ones by Cinchona Squaramide‐Based Organocatalysts
inferred← citeshttps://doi.org/10.1002/ange.201601928openalex-snapshot
Organocatalytic Enantioselective Nucleophilic Alkynylation of Allyl Fluorides Affording Chiral Skipped Ene‐ynes
inferred← citeshttps://doi.org/10.1002/anie.201601928openalex-snapshot
Organocatalytic Enantioselective Nucleophilic Alkynylation of Allyl Fluorides Affording Chiral Skipped Ene‐ynes
inferred← citeshttps://doi.org/10.1002/chem.201700461openalex-snapshot
Attracting Enantiomers: Chiral Analytes That Are Simultaneously Shift Reagents Allow Rapid Screening of Enantiomeric Ratios by NMR Spectroscopy
inferred← citeshttps://doi.org/10.1002/chem.201703308openalex-snapshot
Possible Case of Halogen Bond‐Driven Self‐Disproportionation of Enantiomers (SDE) via Achiral Chromatography
inferred← citeshttps://doi.org/10.1002/chem.202400623openalex-snapshot
Pronounced Self‐Induced Diastereomeric Anisochronism in Anisidine Amino Acid Diamides
inferred← citeshttps://doi.org/10.1002/chir.22683openalex-snapshot
LC–MS/MS and chiroptical spectroscopic analyses of multidimensional metabolic systems of chiral thalidomide and its derivatives
inferred← citeshttps://doi.org/10.1002/chir.22982openalex-snapshot
Internal chirality descriptors iR and iS and ire and isi. A proposed notation to extend the usefulness of the R/S system by retaining the sense of stereochemistry in cases of ligand ranking changes
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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/ijch.201600077openalex-snapshot
Self‐disproportionation of Enantiomers (SDE) of Chiral Nonracemic Amides via Achiral Chromatography
inferred← citeshttps://doi.org/10.1007/s00726-018-2664-xopenalex-snapshot
The self-disproportionation of enantiomers (SDE) of α-amino acid derivatives: facets of steric and electronic properties
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/10.1007/s00726-019-02774-7openalex-snapshot
The self-disproportionation of enantiomers (SDE) via column chromatography of β-amino-α,α-difluorophosphonic acid derivatives
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/b978-0-12-815675-9.00010-2openalex-snapshot
Thalidomide and Analogues
inferred← citeshttps://doi.org/10.1016/j.chroma.2016.05.044openalex-snapshot
Self-disproportionation of enantiomers via achiral gravity-driven column chromatography: A case study of N -acyl-α-phenylethylamines
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.cplett.2026.142877openalex-snapshot
A cooperative proton-relay pathway in imide racemization: An electronic-structure perspective
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2016.06.008openalex-snapshot
Detrifluoroacetylative cascade reactions of bicyclic fluoro-enolates with ortho -phthalaldehyde: Aspects of reactivity, diastereo- and enantioselectivity
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2016.07.016openalex-snapshot
Self-Disproportionation of Enantiomers (SDE) via achiral gravity-driven column chromatography of N -fluoroacyl-1-phenylethylamines
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2016.12.007openalex-snapshot
Detrifluoroacetylative generation and chemistry of fluorine containing tertiary enolates
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2020.109515openalex-snapshot
Professor Norio Shibata, Nagoya Institute of Technology – Recipient of the 2019 American Chemical Society Award for Creative Work in Fluorine Chemistry
inferred← citeshttps://doi.org/10.1016/j.tet.2018.01.006openalex-snapshot
Access to the enantiopure pyrrolobenzodiazepine (PBD) dilactam nucleus via self-disproportionation of enantiomers
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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.tetasy.2017.08.020openalex-snapshot
A question of policy: should tests for the self-disproportionation of enantiomers (SDE) be mandatory for reports involving scalemates?
inferred← citeshttps://doi.org/10.1021/acs.cgd.3c01030openalex-snapshot
Chiral Inversion of Thalidomide During Crystal Growth by Sublimation
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Next Generation of Fluorine-Containing Pharmaceuticals, Compounds Currently in Phase II–III Clinical Trials of Major Pharmaceutical Companies: New Structural Trends and Therapeutic Areas
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How Temperature Change Affects the Lattice Parameters, Molecular Conformation, and Reaction Cavity in Enantiomeric and Racemic Crystals of Thalidomide
inferred← citeshttps://doi.org/10.1038/s41598-018-35457-6openalex-snapshot
Understanding the Thalidomide Chirality in Biological Processes by the Self-disproportionation of Enantiomers
inferred← citeshttps://doi.org/10.1039/c6ob01152gopenalex-snapshot
Catalytic cascade aldol–cyclization of tertiary ketone enolates for enantioselective synthesis of keto-esters with a C–F quaternary stereogenic center
inferred← citeshttps://doi.org/10.1039/c6ra21253kopenalex-snapshot
Synthesis of fluorinated donepezil by palladium-catalyzed decarboxylative allylation of α-fluoro-β-keto ester with tri-substituted heterocyclic alkene and the self-disproportionation of its enantiomers
inferred← citeshttps://doi.org/10.1039/c7sc05138gopenalex-snapshot
The self-disproportionation of enantiomers (SDE): a menace or an opportunity?
inferred← citeshttps://doi.org/10.1107/s2056989018014317openalex-snapshot
Crystal structure of the thalidomide analog (3aR*,7aS*)-2-(2,6-dioxopiperidin-3-yl)hexahydro-1H-isoindole-1,3(2H)-dione
inferred← citeshttps://doi.org/10.1246/bcsj.20160223openalex-snapshot
Development of Shelf-Stable Reagents for Fluoro-Functionalization Reactions
inferred← citeshttps://doi.org/10.1371/journal.pone.0182152openalex-snapshot
Biological evaluation of both enantiomers of fluoro-thalidomide using human myeloma cell line H929 and others
inferred← citeshttps://doi.org/10.24820/ark.5550190.p009.829openalex-snapshot
Self-disproportionation of enantiomers (SDE) of chiral sulfur-containing compounds via achiral chromatography
inferred← citeshttps://doi.org/10.3390/cryst10070606openalex-snapshot
The Solid-State Structures of Cyclic NH Carboximides
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
inferred← citeshttps://doi.org/10.3762/bjoc.21.54openalex-snapshot
Origami with small molecules: exploiting the C–F bond as a conformational tool
inferred← citeshttps://doi.org/10.5530/ijper.54.4.209openalex-snapshot
An in-depth Study of the Concept of Chirality in Organic and Pharmaceutical Chemistry: Using Crystal Structure Data with 3D Visualization Software
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