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Recommended Tests for the Self-Disproportionation of Enantiomers (SDE) to Ensure Accurate Reporting of the Stereochemical Outcome of Enantioselective Reactions
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Nonlinear Effects in Asymmetric Synthesis and Stereoselective Reactions: Ten Years of Investigation
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Assembly of Fluorinated Quaternary Stereogenic Centers through Catalytic Enantioselective Detrifluoroacetylative Aldol Reactions
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Possible Case of Halogen Bond‐Driven Self‐Disproportionation of Enantiomers (SDE) via Achiral Chromatography
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Enantiomer‐Differentiation Induced by an Enantiomeric Excess during Chromatography with Achiral Phases
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Self-disproportionation of Enantiomers of Enantiomerically Enriched Compounds
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Remarkable magnitude of the self-disproportionation of enantiomers (SDE) via achiral chromatography: application to the practical-scale enantiopurification of β-amino acid esters
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The self-disproportionation of enantiomers (SDE) via column chromatography of β-amino-α,α-difluorophosphonic acid derivatives
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Tailor-made amino acid-derived pharmaceuticals approved by the FDA in 2019
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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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Resolution of non-racemic mixtures in achiral chromatographic systems: A model for, the enantioselective effects observed
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Enantiomeric enrichment by the use of density differences between racemic compounds and optically active enantiomers
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Catalytic asymmetric synthesis of binaphthol derivatives by aerobic oxidative coupling of 3-hydroxy-2-naphthoates with chiral diamine-copper complex
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Fluorine-containing drugs approved by the FDA in 2019
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General model for the achiral chromatography of enantiomers forming dimers: application to binaphthol
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Elaborate treatment of retention in chemoselective chromatography—The retention increment approach and non-linear effects
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Self-disproportionation of enantiomers of (R)-ethyl 3-(3,5-dinitrobenzamido)-4,4,4-trifluorobutanoate on achiral silica gel stationary phase
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Catalytic asymmetric synthesis of α-(trifluoromethyl)benzylamine via cinchonidine derived base-catalyzed biomimetic 1,3-proton shift reaction
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Self-disproportionation of enantiomers of 3,3,3-trifluorolactic acid amides via sublimation
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Self-disproportionation of enantiomers of α-trifluoromethyl lactic acid amides via sublimation
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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
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Self-disproportionation of enantiomers of isopropyl 3,3,3-(trifluoro)lactate via sublimation: Sublimation rates vs. enantiomeric composition
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Self-disproportionation of enantiomers of heterocyclic compounds having a tertiary trifluoromethyl alcohol center on chromatography with a non-chiral system
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Discrimination of enantiomeric excess of optically active trifluorolactate by distillation: Evidence for a multi-center hydrogen bonding network in the liquid state
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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?
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Successful fluorine-containing herbicide agrochemicals
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Recent advances in the trifluoromethylation methodology and new CF3-containing drugs
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Catalytic asymmetric detrifluoroacetylative aldol reactions of aliphatic aldehydes for construction of C-F quaternary stereogenic centers
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Self-Disproportionation of Enantiomers (SDE) via achiral gravity-driven column chromatography of N -fluoroacyl-1-phenylethylamines
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Detrifluoroacetylative generation and chemistry of fluorine containing tertiary enolates
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Self-disproportionation of enantiomers of non-racemic chiral amine derivatives through achiral chromatography
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Trifluoromethyl aldimines: an overview in the last ten years
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Asymmetric Michael addition reaction organocatalyzed by stereoisomeric pyrrolidine sulfinamides under neat conditions. A brief study of self-disproportionation of enantiomers
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Access to the enantiopure pyrrolobenzodiazepine (PBD) dilactam nucleus via self-disproportionation of enantiomers
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Enantiodifferentiation of phytoalexin spirobrassinin derivatives using the chiral solvating agent (R)-(+)-1,1′-bi-2-naphthol in conjunction with molecular modeling
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Rational application of self-disproportionation of enantiomers via sublimation—a novel methodological dimension for enantiomeric purifications
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Self-disproportionation of enantiomers of prazoles via achiral, gravity-driven silica gel column chromatography
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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
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A question of policy: should tests for the self-disproportionation of enantiomers (SDE) be mandatory for reports involving scalemates?
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Chiral initiator-induces self-disproportionation of enantiomers via achiral chromatography: application to enantiomer separation of racemate
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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
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Self-amplification of optical activity by chromatography on an achiral adsorbent
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Enantiomeric enrichment of α-amino acid derivatives: recrystallization of N-Fmoc α-amino acid tert-butyl esters
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Biomimetic transamination of α-keto perfluorocarboxylic esters. An efficient preparative synthesis of β,β,β-trifluoroalanine
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Chiral sulfoxide controlled asymmetric additions to CN double bond. An efficient approach to stereochemically defined α-fluoroalkyl amino compounds
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Stereoselective synthesis of conformationally constrained reverse turn dipeptide mimetics
inferredcites →https://doi.org/10.1016/s0040-4039(00)73320-xopenalex-snapshot
Catalytic asymmetric synthesis of β-fluoroalkyl-β-amino acids via biomimetic [1,3]-proton shift reaction
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Transamination of fluorinated β-keto carboxylic esters. A biomimetic approach to β-polyfluoroalkyl-β-amino acids.
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A highly stereoselective synthesis of s(-)-[1,1′-binaphthalene]-2,2′-diol
inferredcites →https://doi.org/10.1016/s0957-4166(98)00168-2openalex-snapshot
Nonlinear effects as `indicators' in the tuning of asymmetric catalysts
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Intellectual property and chirality of drugs
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Self-induced chiral recognition in the association of enantiomeric mixtures on silica gel chromatography
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Chemical Aspects of Human and Environmental Overload with Fluorine
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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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Chiral Organosulfur Ligands/Catalysts with a Stereogenic Sulfur Atom: Applications in Asymmetric Synthesis
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Localized Partitioning of Enantiomers in Solid Samples of Sulfoxides: Importance of Sampling Method in Determination of Enantiopurity
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Fluorine in Pharmaceutical Industry: Fluorine-Containing Drugs Introduced to the Market in the Last Decade (2001–2011)
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Enantioselective Synthesis of Sulfoxides: 2000−2009
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Synthesis and Applications of tert-Butanesulfinamide
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On the validity of Wallach's rule: on the density and stability of racemic crystals compared with their chiral counterparts
inferredcites →https://doi.org/10.1021/ja028403hopenalex-snapshot
Homochiral Supramolecular Polymerization of an “S”-Shaped Chiral Monomer: Translation of Optical Purity into Molecular Weight Distribution
inferredcites →https://doi.org/10.1021/ja065603aopenalex-snapshot
Phenomenon of Optical Self-Purification of Chiral Non-Racemic Compounds
inferredcites →https://doi.org/10.1021/ja067905iopenalex-snapshot
Separation of Racemate from Excess Enantiomer of Chiral Nonracemic Compounds via Density Gradient Ultracentrifugation
inferredcites →https://doi.org/10.1021/ja1018628openalex-snapshot
Stereoselective Construction of Halogenated Quaternary Stereogenic Centers via Catalytic Asymmetric Diels−Alder Reaction
inferredcites →https://doi.org/10.1021/ja104184ropenalex-snapshot
Photopromoted Ru-Catalyzed Asymmetric Aerobic Sulfide Oxidation and Epoxidation Using Water as a Proton Transfer Mediator
inferredcites →https://doi.org/10.1021/ja304806jopenalex-snapshot
Highly Enantioselective Chlorination of β-Keto Esters and Subsequent SN2 Displacement of Tertiary Chlorides: A Flexible Method for the Construction of Quaternary Stereogenic Centers
inferredcites →https://doi.org/10.1021/jo00081a015openalex-snapshot
Enantiomeric enrichment of sulfoxides by preparative flash chromatography on an achiral phase
inferredcites →https://doi.org/10.1021/jo00427a033openalex-snapshot
Enhancement of optical activity by fractional sublimation. An alternative to fractional crystallization and a warning
inferredcites →https://doi.org/10.1021/jo01281a037openalex-snapshot
Separation of an enantiomorph and its racemate by sublimation
inferredcites →https://doi.org/10.1021/jo0155052openalex-snapshot
Synthesis, Absolute Configuration, and Enantiomeric Enrichment of a Cruciferous Oxindole Phytoalexin, (S)-(−)-Spirobrassinin, and Its Oxazoline Analog
inferredcites →https://doi.org/10.1021/jo040221dopenalex-snapshot
Efficient Asymmetric Oxidation of Sulfides and Kinetic Resolution of Sulfoxides Catalyzed by a Vanadium−Salan System
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/jo9710238openalex-snapshot
Enantioselective Biomimetic Transamination of β-Keto Carboxylic Acid Derivatives. An Efficient Asymmetric Synthesis of β-(Fluoroalkyl) β-Amino Acids
inferredcites →https://doi.org/10.1021/jo981808topenalex-snapshot
Enantioselective Synthesis of Binaphthol Derivatives by Oxidative Coupling of Naphthol Derivatives Catalyzed by Chiral Diamine·Copper Complexes
inferredcites →https://doi.org/10.1021/jo991691oopenalex-snapshot
Asymmetric Catalysis of the Friedel−Crafts Reaction with Fluoral by Chiral Binaphthol-Derived Titanium Catalysts through Asymmetric Activation
inferredcites →https://doi.org/10.1021/jp020352nopenalex-snapshot
Measurement of the Dimerization Equilibrium Constants of Enantiomers
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Enantiomeric Excess of a Cruciferous Phytoalexin, Spirobrassinin, and Its Enantiomeric Enrichment in an Achiral HPLC System
inferredcites →https://doi.org/10.1021/ol0521681openalex-snapshot
Using Enzyme Inhibition as a High Throughput Method to Measure the Enantiomeric Excess of a Chiral Sulfoxide
inferredcites →https://doi.org/10.1021/ol201007eopenalex-snapshot
Enantioselective gem -Chlorofluorination of Active Methylene Compounds Using a Chiral Spiro Oxazoline Ligand
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Understanding the Thalidomide Chirality in Biological Processes by the Self-disproportionation of Enantiomers
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A study of asymmetric protonation with chiral β-hydroxy sulfoxides. Asymmetric synthesis of (–)-epibatidine
inferredcites →https://doi.org/10.1039/a707196eopenalex-snapshot
Synthesis, enzymic resolution and enantiomeric enhancement of bis(hydroxymethyl)[7]thiaheterohelicenes
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Role of sulfur chirality in the chemical processes of biology
inferredcites →https://doi.org/10.1039/b709314bopenalex-snapshot
Spoilt for choice: assessing phase behavior models for the evolution of homochirality
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/c0cp01155jopenalex-snapshot
Theoretical investigations into the enantiomeric and racemic forms of α-(trifluoromethyl)lactic acid
inferredcites →https://doi.org/10.1039/c1cc10403aopenalex-snapshot
Highly enantioselective zinc/BINOL-catalyzed alkynylation of α-ketoimine ester: a new entry to optically active quaternary α-CF 3 α-amino acids
inferredcites →https://doi.org/10.1039/c2cc32757kopenalex-snapshot
Practical synthesis of 4,4,4-trifluorocrotonaldehyde: a versatile precursor for the enantioselective formation of trifluoromethylated stereogenic centers via organocatalytic 1,4-additions
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/c4cc02604gopenalex-snapshot
Separation and enrichment of enantiopure from racemic compounds using magnetic levitation
inferredcites →https://doi.org/10.1039/c4cs00524dopenalex-snapshot
The emergence of sulfoxides as efficient ligands in transition metal catalysis
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/c4ra13928copenalex-snapshot
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-snapshot
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/c6cs00703aopenalex-snapshot
Chiral sulfoxides: advances in asymmetric synthesis and problems with the accurate determination of the stereochemical outcome
inferredcites →https://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
inferredcites →https://doi.org/10.1039/c6ob02454hopenalex-snapshot
Catalytic asymmetric aldol addition reactions of 3-fluoro-indolinone derived enolates
inferredcites →https://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
inferredcites →https://doi.org/10.1039/c7cs00555eopenalex-snapshot
Enantiomer surface chemistry: conglomerate versus racemate formation on surfaces
inferredcites →https://doi.org/10.1039/c7sc05138gopenalex-snapshot
The self-disproportionation of enantiomers (SDE): a menace or an opportunity?
inferredcites →https://doi.org/10.1039/c9ce00320gopenalex-snapshot
Chirality-dependent halogen bonds in axially chiral quinazolin-4-one derivatives bearing ortho -halophenyl groups
inferredcites →https://doi.org/10.1055/s-0030-1259018openalex-snapshot
On the Practical Limits of Determining Isolated Product Yields and Ratios of Stereoisomers: Reflections, Analysis, and Redemption
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/10.1071/ch9920651openalex-snapshot
Partially Racemic Compounds as Brushtail Possum Urinary Metabolites
inferredcites →https://doi.org/10.1080/10426509608038790openalex-snapshot
RECENT ADVANCES IN THE SYNTHESIS OF SULFOXIDES FROM SULFIDES
inferredcites →https://doi.org/10.1080/10826079208018806openalex-snapshot
Resolution of Enantiomers with Achiral Phase Chromatography
inferredcites →https://doi.org/10.1080/17415993.2012.725247openalex-snapshot
Asymmetric oxidation of sulfides
inferredcites →https://doi.org/10.1142/9781786347336_0006openalex-snapshot
The Role of Fluorine in the Self-Disproportionation of Enantiomers (SDE) Phenomenon of Scalemic Samples of Fluoroorganics
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.2001.1330openalex-snapshot
Chiral Recognition by Multicenter Single Proton Hydrogen Bonding of Trifluorolactates
inferredcites →https://doi.org/10.2165/00003495-199856030-00002openalex-snapshot
Proton Pump Inhibitors
inferredcites →https://doi.org/10.2174/157017911794697277openalex-snapshot
Biomimetic Transamination – a Metal-Free Alternative to the Reductive Amination. Application for Generalized Preparation of Fluorine-Containing Amines and Amino Acids
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/10.24820/ark.5550190.p009.829openalex-snapshot
Self-disproportionation of enantiomers (SDE) of chiral sulfur-containing compounds via achiral chromatography
inferredcites →https://doi.org/10.31635/ccschem.021.202000664openalex-snapshot
Organocatalytic Stereoselective [8+2] Cycloaddition of Tropones with Azlactones
inferredcites →https://doi.org/10.3390/molecules25020405openalex-snapshot
The Synthesis of α-Aminophosphonates via Enantioselective Organocatalytic Reaction of 1-(N-Acylamino)alkylphosphonium Salts with Dimethyl Phosphite
inferredcites →https://doi.org/10.3390/sym11050680openalex-snapshot
A General Phenomenon of Spontaneous Amplification of Optical Purity under Achiral Chromatographic Conditions
inferredcites →https://doi.org/10.3390/sym12071106openalex-snapshot
Potentially Mistaking Enantiomers for Different Compounds Due to the Self-Induced Diastereomeric Anisochronism (SIDA) Phenomenon
inferredcites →https://doi.org/10.3390/sym13040543openalex-snapshot
Flurbiprofen: A Study of the Behavior of the Scalemate by Chromatography, Sublimation, and NMR
inferredcites →https://doi.org/10.3390/sym13040667openalex-snapshot
The Stoichiometry, Structure and Possible Formation of Crystalline Diastereomeric Salts
inferredcites →https://doi.org/10.3998/ark.5550190.0012.101openalex-snapshot
Synthesis of enantioenriched sulfoxides
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/adsc.202100493openalex-snapshot
DBU Catalysed Enantioselective Degradative Rearrangement: a Way to Tetrasubstituted 2‐Aryl‐2‐Amino Esters
inferred← citeshttps://doi.org/10.1002/adsc.202201268openalex-snapshot
Evolution and Future of Hetero‐ and Hydro‐Trifluoromethylations of Unsaturated C−C Bonds
inferred← citeshttps://doi.org/10.1002/chem.202500662openalex-snapshot
Fluorine in the Pharmaceutical Industry: FDA‐Approved Fluorine‐Containing Drugs in 2024
inferred← citeshttps://doi.org/10.1002/chir.23376openalex-snapshot
New pharmaceuticals approved by FDA in 2020: Small‐molecule drugs derived from amino acids and related compounds
inferred← citeshttps://doi.org/10.1002/cjoc.202100824openalex-snapshot
Stereodivergent Synthesis of Carbocyclic Quaternary α‐Amino Acid Derivatives Containing Two Contiguous Stereocenters
inferred← citeshttps://doi.org/10.1016/j.cclet.2022.06.001openalex-snapshot
Fluorine-containing drugs approved by the FDA in 2021
inferred← citeshttps://doi.org/10.1016/j.cclet.2024.109780openalex-snapshot
FDA approved fluorine-containing drugs in 2023
inferred← citeshttps://doi.org/10.1016/j.chempr.2023.02.022openalex-snapshot
NMR in operando monitoring of mechanochemically accelerated sublimations
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.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.2022.109978openalex-snapshot
Successful trifluoromethoxy-containing pharmaceuticals and agrochemicals
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.145422openalex-snapshot
Synthesis of five-membered, CF3-containing lactones: structural and biological examinations
inferred← citeshttps://doi.org/10.1039/d5ob01564bopenalex-snapshot
A one-pot visible-light strategy for cyclobutanone synthesis via sequential [2 + 2] cycloaddition and Nef reaction of nitroalkenes and 2-vinylpyridines
inferred← citeshttps://doi.org/10.15407/bioorganica2023.02.003openalex-snapshot
Discovery of biomimetic transamination as a general synthetic method for preparation of fluorine-containing amines and amino acids
inferred← citeshttps://doi.org/10.15407/bioorganica2024.01.003openalex-snapshot
New drugs appearing on the market in 2023: molecules containing fluorine and fragments of tailor-made amino acids
inferred← citeshttps://doi.org/10.15407/bioorganica2024.01.021openalex-snapshot
Enzymatic approaches for preparation of α-aminophosphonic acids and fluorine-containing β-amino acids
inferred← citeshttps://doi.org/10.33609/2708-129x.91.10.2025.27-71openalex-snapshot
CUTTING-EDGE STRATEGIES IN THE ASYMMETRIC SYNTHESIS OF α-AMINOCYCLOPROPANE CARBOXYLIC ACIDS: ESSENTIAL SCAFFOLDS FOR DRUG DISCOVERY
inferred← citeshttps://doi.org/10.33609/2708-129x.91.12.2025.33-72openalex-snapshot
ENANTIOSELECTIVE CATALYSIS FOR THE SYNTHESIS OF 1-SUBSTITUTED-2,2,2-TRIFLUOROETHYLAMINES
inferred← citeshttps://doi.org/10.33609/2708-129x.91.2.2025.55-90openalex-snapshot
CHIRAL, FLUORINE-CONTAINING PHARMACEUTICALS
inferred← citeshttps://doi.org/10.33609/2708-129x.91.3.2025.34-48openalex-snapshot
ENANTIOMER PURIFICATION THROUGH ACHIRAL CHROMATOGRAPHY: INTEGRATING SIMULATED MOVING BED AND SELF-DISPROPORTIONATION OF ENANTIOMERS
inferred← citeshttps://doi.org/10.33609/2708-129x.91.6.2025.15-54openalex-snapshot
MODERN PHARMACEUTICAL DRUGS FEATURING ALIPHATIC FLUORINE-CONTAINING GROUPS
inferred← citeshttps://doi.org/10.33609/2708-129x.91.8.2025.36-64openalex-snapshot
SYNTHESIS OF TAILOR-MADE AMINO ACIDS CONTAINING C(sp2)–F BONDS
inferred← citeshttps://doi.org/10.33609/2708-129x.92.4.2026.52-78openalex-snapshot
ORGANOFLUORINE CHEMISTRY IN ONCOLOGY: A REVIEW OF US FDA-APPROVED ANTICANCER DRUGS IN 2025 (review)
inferred← citeshttps://doi.org/10.33609/2708-129x.92.5.2026.31-63openalex-snapshot
APPLICATION OF D-AMINO ACIDS IN DRUG DESIGN (review)
inferred← citeshttps://doi.org/10.3389/fspas.2024.1427260openalex-snapshot
On the correlation between the enantiomeric excess of L-isovaline and the level of aqueous alteration in carbonaceous meteorites
inferred← citeshttps://doi.org/10.3390/molecules26133994openalex-snapshot
A Call for a Change in Policy Regarding the Necessity for SDE Tests to Validate the Veracity of the Outcome of Enantioselective Syntheses, the Inherent Chiral State of Natural Products, and Other Cases Involving Enantioenriched Samples
inferred← citeshttps://doi.org/10.3390/molecules26175166openalex-snapshot
Application of Polyamines and Amino Acid Derivatives Based on 2-Azabicycloalkane Backbone in Enantioselective Aldol Reaction
inferred← citeshttps://doi.org/10.3390/molecules27030825openalex-snapshot
Special Issue “Feature Review Papers in Organic Synthesis”
inferred← citeshttps://doi.org/10.3390/molecules27123797openalex-snapshot
Asymmetric Michael Addition in Synthesis of β-Substituted GABA Derivatives
inferred← citeshttps://doi.org/10.3390/molecules28041584openalex-snapshot
Enantioseparation of P-Stereogenic 1-Adamantyl Arylthiophosphonates and Their Stereospecific Transformation to 1-Adamantyl Aryl-H-phosphinates
inferred← citeshttps://doi.org/10.3390/molecules28052115openalex-snapshot
Experimental Determination of a Chiral Ternary Solubility Diagram and Its Interpretation in Gas Antisolvent Fractionation
inferred← citeshttps://doi.org/10.3390/molecules28062694openalex-snapshot
Catalytic Asymmetric α-Functionalization of α-Branched Aldehydes
inferred← citeshttps://doi.org/10.3390/ph15080999openalex-snapshot
The Latest FDA-Approved Pharmaceuticals Containing Fragments of Tailor-Made Amino Acids and Fluorine
inferred← citeshttps://doi.org/10.3390/separations10070382openalex-snapshot
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
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