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Access to the enantiopure pyrrolobenzodiazepine (PBD) dilactam nucleus via self-disproportionation 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.200503373openalex-snapshot
Remarkable Amplification of the Self‐Disproportionation of Enantiomers on Achiral‐Phase Chromatography Columns
inferredcites →https://doi.org/10.1002/anie.201510610openalex-snapshot
From Anthramycin to Pyrrolobenzodiazepine (PBD)‐Containing Antibody–Drug Conjugates (ADCs)
inferredcites →https://doi.org/10.1002/chem.200501128openalex-snapshot
Synthesis and Evaluation of Acyl Protein Thioesterase 1 (APT1) Inhibitors
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/ejoc.201100409openalex-snapshot
Cooperative Catalysis for the First Asymmetric Formal [3+2] Cycloaddition Reaction of Isocyanoacetates to α,β‐Unsaturated Ketones
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/hlca.201400122openalex-snapshot
Terminology Related to the Phenomenon ‘Self‐Disproportionation of Enantiomers’ (SDE)
inferredcites →https://doi.org/10.1002/hlca.201500041openalex-snapshot
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/10.1002/ijch.201600077openalex-snapshot
Self‐disproportionation of Enantiomers (SDE) of Chiral Nonracemic Amides via Achiral Chromatography
inferredcites →https://doi.org/10.1002/med.20212openalex-snapshot
Biosynthesis, synthesis, and biological activities of pyrrolobenzodiazepines
inferredcites →https://doi.org/10.1007/128_2013_434openalex-snapshot
Self-disproportionation of Enantiomers of Enantiomerically Enriched Compounds
inferredcites →https://doi.org/10.1007/s00726-015-2152-5openalex-snapshot
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/s11084-013-9333-6openalex-snapshot
Deracemization of Amino Acids by Partial Sublimation and via Homochiral Self-Organization
inferredcites →https://doi.org/10.1016/j.bmc.2007.01.054openalex-snapshot
Synthesis of a novel C2-aryl pyrrolo[2,1-c][1,4]benzodiazepine-5,11-dione library: Effect of C2-aryl substitution on cytotoxicity and non-covalent DNA binding
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.2009.11.010openalex-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.2009.12.008openalex-snapshot
Attempts to explain the self-disproportionation observed in the partial sublimation of enantiomerically enriched carboxylic acids
inferredcites →https://doi.org/10.1016/j.tet.2004.07.040openalex-snapshot
Synthetic study of (+)-anthramycin using ring-closing enyne metathesis and cross-metathesis
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.tetasy.2017.08.020openalex-snapshot
A question of policy: should tests for the self-disproportionation of enantiomers (SDE) be mandatory for reports involving scalemates?
inferredcites →https://doi.org/10.1021/acschembio.7b00335openalex-snapshot
Diversity of Alkylproline Moieties in Pyrrolobenzodiazepines Arises from Postcondensation Modifications of a Unified Building Block
inferredcites →https://doi.org/10.1021/cc0501458openalex-snapshot
Solid-Phase Synthesis of a Library of Pyrrolo[2,1-c][1,4]benzodiazepine-5,11-diones with Potential Antitubercular Activity
inferredcites →https://doi.org/10.1021/cr100120fopenalex-snapshot
Synthesis of DNA-Interactive Pyrrolo[2,1-c][1,4]benzodiazepines (PBDs)
inferredcites →https://doi.org/10.1021/ja065603aopenalex-snapshot
Phenomenon of Optical Self-Purification of Chiral Non-Racemic Compounds
inferredcites →https://doi.org/10.1021/jm901722vopenalex-snapshot
Structure−Activity Relationships of Monomeric C2-Aryl Pyrrolo[2,1-c][1,4]benzodiazepine (PBD) Antitumor Agents
inferredcites →https://doi.org/10.1021/jo00026a035openalex-snapshot
Synthesis of (.+-.)-.alpha.-allokainic acid via the zinc acetate catalyzed cyclization of .gamma.-isocyano silyl enolates
inferredcites →https://doi.org/10.1021/np800827wopenalex-snapshot
Limazepines A−F, Pyrrolo[1,4]benzodiazepine Antibiotics from an Indonesian Micrococcus sp.
inferredcites →https://doi.org/10.1039/b616196kopenalex-snapshot
Serine sublimes with spontaneous chiral amplification
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/c39750000742openalex-snapshot
Synthesis of the 5,11-dioxo-1H-pyrrolo[2,1-c][1,4]benzodiazepine nucleus of anthramycin and related natural products
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/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/10.1111/jam.12136openalex-snapshot
Neuraminidase Inhibitors from marine-derived actinomycete Streptomyces seoulensis
inferredcites →https://doi.org/10.1517/13543784.2011.573477openalex-snapshot
The development of pyrrolobenzodiazepines as antitumour agents
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/10.3390/molecules21020154openalex-snapshot
An Update on the Synthesis of Pyrrolo[1,4]benzodiazepines
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/chem.201801670openalex-snapshot
Palladium‐Catalyzed Asymmetric Allylic Alkylations of Colby Pro‐Enolates with MBH Carbonates: Enantioselective Access to Quaternary C−F Oxindoles
inferred← citeshttps://doi.org/10.1002/ejoc.202000890openalex-snapshot
Recent Advances in the Chemistry of Isocyanides with Activated Methylene Group
inferred← citeshttps://doi.org/10.1007/s00044-023-03177-wopenalex-snapshot
Pyrrolobenzodiazepines: natural sources, therapeutic uses, and future in neurological treatments
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/b978-0-12-819962-6.00016-6openalex-snapshot
Seven-Membered Rings
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.ejmech.2019.111826openalex-snapshot
Applications of fluorine-containing amino acids for drug design
inferred← citeshttps://doi.org/10.1039/d2ob01117dopenalex-snapshot
Synthesis of bridgehead-azacycles via dual C–N/C–C annulation of α-amino acids, aminals and maleimides
inferred← citeshttps://doi.org/10.14201/gredos.159160openalex-snapshot
Aplicación de nuevas isoxazolidinas quirales en síntesis orientada a la diversidad
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/10.3390/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/10.3390/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/molecules28155908openalex-snapshot
Copper (II) Ions Induced Self-Disproportionation of Enantiomers in Capillary Electrophoresis for the Quantification of Atenolol Enantiomers
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
inferred← citeshttps://doi.org/10.3390/sym13040543openalex-snapshot
Flurbiprofen: A Study of the Behavior of the Scalemate by Chromatography, Sublimation, and NMR
inferred← citeshttps://doi.org/10.3390/sym18040699openalex-snapshot
Investigation of Self-Disproportionation of Enantiomers via Column Chromatography (SDEvCC) Using 3-(ortho-Substituted-phenyl)quinazolin-4-one Derivatives
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