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Oxetanes in Drug Discovery: Structural and Synthetic Insights
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1099-0690(199805)1998:5<925::aid-ejoc925>3.0.co;2-fopenalex-snapshot
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inferredcites →https://doi.org/10.1002/anie.200800450openalex-snapshot
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inferredcites →https://doi.org/10.1002/cbic.200301023openalex-snapshot
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inferredcites →https://doi.org/10.1002/cmdc.200700059openalex-snapshot
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inferredcites →https://doi.org/10.1016/0006-2952(71)90068-2openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmc.2006.05.020openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.molstruc.2003.08.022openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0090-9556(25)06516-xopenalex-snapshot
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inferredcites →https://doi.org/10.1515/ncrs-1999-0461openalex-snapshot
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inferredcites →https://doi.org/10.2533/chimia.2000.640openalex-snapshot
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The Enthalpies of Combustion and Formation of Some 3,3-Disubstituted Oxetanes.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1002/cssc.202501862openalex-snapshot
Copper‐Catalyzed Ring‐Opening Cross‐Coupling of Cyclopropanols with Phosphorothioates
inferred← citeshttps://doi.org/10.1002/ejic.202100168openalex-snapshot
Anticancer Activity and Mode of Action of Copper(II)‐Bis(thiosemicarbazonato) Complexes with Pendant Nitrogen Heterocycles
inferred← citeshttps://doi.org/10.1002/ejoc.201000712openalex-snapshot
Enantiomerically Pure and Highly Substituted Alicyclic α,α‐Difluoro Ketones: Potential Inhibitors for Malarial Aspartic Proteases, the Plasmepsins
inferred← citeshttps://doi.org/10.1002/ejoc.201300121openalex-snapshot
Synthesis and Characterization of β‐Trifluoromethyl‐Substituted Pyrrolidines
inferred← citeshttps://doi.org/10.1002/ejoc.201500172openalex-snapshot
Synthesis of Fluorine‐Containing 3,3‐Disubstituted Oxetanes and Alkylidene Oxetanes
inferred← citeshttps://doi.org/10.1002/ejoc.201601524openalex-snapshot
Schreiner's Thiourea Promoted [2+2] Cycloaddition of Captodative Azetidinones and Nitroolefins
inferred← citeshttps://doi.org/10.1002/ejoc.201701214openalex-snapshot
Stereoselective and Regioselective Pinacol‐Type Rearrangement of a Fused Bicyclic Oxetanol Scaffold
inferred← citeshttps://doi.org/10.1002/ejoc.201900498openalex-snapshot
Catalytic Friedel‐Crafts Reactions on Saturated Heterocycles and Small Rings for sp3‐sp2 Coupling of Medicinally Relevant Fragments
inferred← citeshttps://doi.org/10.1002/ejoc.201900499openalex-snapshot
Synthesis of Spirooxindole Oxetanes Through a Domino Reaction of 3‐Hydroxyoxindoles and Phenyl Vinyl Selenone
inferred← citeshttps://doi.org/10.1002/ejoc.201900949openalex-snapshot
First Direct Evidence of an ortho‐Lithiated Aryloxetane: Solid and Solution Structure, and Dynamics
inferred← citeshttps://doi.org/10.1002/ejoc.202001614openalex-snapshot
Monoprotected Diamines Derived from 1,5‐Disubstituted (Aza)spiro[2.3]hexane Scaffolds
inferred← citeshttps://doi.org/10.1002/ejoc.202100857openalex-snapshot
Emerging Building Blocks for Medicinal Chemistry: Recent Synthetic Advances
inferred← citeshttps://doi.org/10.1002/ejoc.202201275openalex-snapshot
Cu(OTf)2/NBS Promoted Cyclization of 1‐Cinnamyl Alcohol‐o‐Carboranes: An Efficient Approach for Synthesis ofo‐Carboranes Substituted Oxetanes
inferred← citeshttps://doi.org/10.1002/ejoc.202501098openalex-snapshot
Catalytic Asymmetric Synthesis of Vicinal Chiral Carbonyl Bioisosteres
inferred← citeshttps://doi.org/10.1002/open.202200083openalex-snapshot
Strain and Complexity, Passerini and Ugi Reactions of Four‐Membered Heterocycles and Further Elaboration of TOSMIC Product
inferred← citeshttps://doi.org/10.1007/7081_2015_5006openalex-snapshot
Synthesis of Oxygenated Heterocyclic Compounds via Gold-Catalyzed Functionalization of π-Systems
inferred← citeshttps://doi.org/10.1007/7355_2013_29openalex-snapshot
The Influence of Bioisosteres in Drug Design: Tactical Applications to Address Developability Problems
inferred← citeshttps://doi.org/10.1007/978-1-62703-730-3_11openalex-snapshot
Probing Riboswitch Binding Sites with Molecular Docking, Focused Libraries, and In-line Probing Assays
inferred← citeshttps://doi.org/10.1007/s00253-014-6003-1openalex-snapshot
Tyrosine kinase inhibitor Thiotanib targets Bcr-Abl and induces apoptosis and autophagy in human chronic myeloid leukemia cells
inferred← citeshttps://doi.org/10.1007/s00253-018-09576-zopenalex-snapshot
Oxetane-containing metabolites: origin, structures, and biological activities
inferred← citeshttps://doi.org/10.1007/s00726-013-1521-1openalex-snapshot
A compendium of cyclic sugar amino acids and their carbocyclic and heterocyclic nitrogen analogues
inferred← citeshttps://doi.org/10.1007/s10822-018-0183-1openalex-snapshot
Uncovering abnormal changes in logP after fluorination using molecular dynamics simulations
inferred← citeshttps://doi.org/10.1007/s11696-017-0194-8openalex-snapshot
Influence of the nature of the substituent in 3-(2-pyridyl)-1,2,4-triazole for complexation with Pd2+
inferred← citeshttps://doi.org/10.1007/s11696-017-0237-1openalex-snapshot
An efficient synthesis of structurally diverse 2-methyl-N-[(3-phenylamino)oxetan-3-yl]-2-propanesulfinamide derivatives under catalyst free conditions
inferred← citeshttps://doi.org/10.1007/s43630-021-00129-4openalex-snapshot
Catalyst-free [2 + 2] photocycloadditions between benzils and olefins under visible light
inferred← citeshttps://doi.org/10.1016/b978-0-08-096805-6.00004-8openalex-snapshot
Four-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00830-2openalex-snapshot
8.28 Reduction of SulfurCarbon Bonds and of Other Heteroatoms Bonded to Tetrahedral Carbon
inferred← citeshttps://doi.org/10.1016/b978-0-08-099406-2.00003-0openalex-snapshot
Four-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-382030-3.00002-7openalex-snapshot
Lead Discovery and Lead Modification
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.12291-7openalex-snapshot
Spirocyclic Scaffolds in Drug Discovery
inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00150-5openalex-snapshot
Oxetanes and Oxetenes: Fused-Ring Derivatives
inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00162-1openalex-snapshot
Oxetanes and Oxetenes: Monocyclic
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00163-0openalex-snapshot
Reduction of Sulfur–Carbon Bonds and of Other Heteroatoms Bonded to Tetrahedral Carbon
inferred← citeshttps://doi.org/10.1016/b978-0-443-13259-9.00013-3openalex-snapshot
Synthesis of azetines and oxetanes
inferred← citeshttps://doi.org/10.1016/b978-0-443-18947-0.00003-1openalex-snapshot
Synthesis of oxetanes from epoxides
inferred← citeshttps://doi.org/10.1016/b978-0-443-18947-0.00004-3openalex-snapshot
Synthesis of oxetanes from carbonyl compounds
inferred← citeshttps://doi.org/10.1016/b978-0-443-18947-0.00007-9openalex-snapshot
Synthesis of oxetanes by addition of ene and yne compounds to carbonyl compounds
inferred← citeshttps://doi.org/10.1016/b978-0-443-18947-0.00008-0openalex-snapshot
Synthesis of oxetanes under photochemical irradiation
inferred← citeshttps://doi.org/10.1016/b978-0-443-18947-0.00010-9openalex-snapshot
Synthesis of oxetanes from halo alcohols
inferred← citeshttps://doi.org/10.1016/b978-0-443-18947-0.00011-0openalex-snapshot
Synthesis of oxetanes from alcohols
inferred← citeshttps://doi.org/10.1016/b978-0-443-18947-0.00012-2openalex-snapshot
Synthesis of oxetanes from acid, alcohol, and carbonyl moiety-containing compounds
inferred← citeshttps://doi.org/10.1016/b978-0-443-18947-0.00017-1openalex-snapshot
Synthesis of oxetanes from ketenes—Part I
inferred← citeshttps://doi.org/10.1016/b978-0-443-23932-8.00028-5openalex-snapshot
Verquvo, a first-in-class soluble guanylate cyclase stimulator for the treatment of heart failure
inferred← citeshttps://doi.org/10.1016/b978-0-443-27684-2.00001-7openalex-snapshot
Synthesis of azetidines from halo and amine moieties bearing compounds
inferred← citeshttps://doi.org/10.1016/bs.aihch.2015.10.003openalex-snapshot
Recent Developments in the Lithiation Reactions of Oxygen Heterocycles
inferred← citeshttps://doi.org/10.1016/bs.aihch.2016.03.004openalex-snapshot
Saturated Heterocycles with Applications in Medicinal Chemistry
inferred← citeshttps://doi.org/10.1016/bs.aihch.2024.04.004openalex-snapshot
Recent advances in the synthesis of 3,3-disubstituted oxetanes
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103210openalex-snapshot
Spirocyclic sulfonamides with carbonic anhydrase inhibitory and anti-neuropathic pain activity
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103578openalex-snapshot
Morpholine as ubiquitous pharmacophore in medicinal chemistry: Deep insight into the structure-activity relationship (SAR)
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104425openalex-snapshot
Synthetic and medicinal chemistry of phthalazines: Recent developments, opportunities and challenges
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107458openalex-snapshot
Design and synthesis of sulfonamide phenothiazine derivatives as novel ferroptosis inhibitors and their therapeutic effects in spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.biopha.2022.112894openalex-snapshot
Development of vericiguat: The first soluble guanylate cyclase (sGC) stimulator launched for heart failure with reduced ejection fraction (HFrEF)
inferred← citeshttps://doi.org/10.1016/j.bmc.2013.06.032openalex-snapshot
Design and synthesis of novel 1,25-dihydroxyvitamin D3 analogues having a spiro-oxetane fused at the C2 position in the A-ring
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.05.021openalex-snapshot
Lead identification of benzimidazolone and azabenzimidazolone arylsulfonamides as CC-chemokine receptor 4 (CCR4) antagonists
inferred← citeshttps://doi.org/10.1016/j.bmc.2017.12.012openalex-snapshot
Densely functionalised spirocyclic oxetane-piperidine scaffolds for drug discovery
inferred← citeshttps://doi.org/10.1016/j.bmc.2023.117400openalex-snapshot
Structure Guided Design, Synthesis, and Biological Evaluation of Oxetane-Containing Indole Analogues
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.04.020openalex-snapshot
Discovery of novel tetracyclic compounds as anaplastic lymphoma kinase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2013.03.032openalex-snapshot
Discovery of ML326: The first sub-micromolar, selective M5 PAM
inferred← citeshttps://doi.org/10.1016/j.bmcl.2013.07.049openalex-snapshot
Four-membered heterocycles-containing 4-anilino-quinazoline derivatives as epidermal growth factor receptor (EGFR) kinase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2014.06.081openalex-snapshot
The use of spirocyclic scaffolds in drug discovery
inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.05.009openalex-snapshot
Synthesis and evaluation of novel benzylphthalazine derivatives as hedgehog signaling pathway inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2019.07.033openalex-snapshot
Applications of amide isosteres in medicinal chemistry
inferred← citeshttps://doi.org/10.1016/j.bmcl.2021.128111openalex-snapshot
1-Aminomethyl SAR in a novel series of flavagline-inspired eIF4A inhibitors: Effects of amine substitution on cell potency and in vitro PK properties
inferred← citeshttps://doi.org/10.1016/j.bmcl.2022.129014openalex-snapshot
Development of a putative Zn2+-chelating but highly selective MMP-13 inhibitor
inferred← citeshttps://doi.org/10.1016/j.bmcl.2023.129218openalex-snapshot
Design, synthesis, and antitumor evaluation of morpholine substituted bisnaphthalimides as DNA targeting agents
inferred← citeshttps://doi.org/10.1016/j.cclet.2024.109498openalex-snapshot
Photochemical reactions as synthetic tool for pharmaceutical industries
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.07.001openalex-snapshot
Design, synthesis and biological evaluation of novel azaspiro analogs of linezolid as antibacterial and antitubercular agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.11.037openalex-snapshot
Synthesis and anticancer activity of novel water soluble benzimidazole carbamates
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113316openalex-snapshot
Discovery of novel N-benzylbenzamide derivatives as tubulin polymerization inhibitors with potent antitumor activities
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.114028openalex-snapshot
Modulating physicochemical properties of tetrahydropyridine-2-amine BACE1 inhibitors with electron-withdrawing groups: A systematic study
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.115616openalex-snapshot
Synthesis and evaluation of dihydrofuro[2,3-b]pyridine derivatives as potent IRAK4 inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.115802openalex-snapshot
Applications of oxetanes in drug discovery and medicinal chemistry
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.117991openalex-snapshot
N-(3-Hydroxyphenyl)-3,8-diazabicyclooctanes as opioid receptors probes. 1. Investigation of the phenolic hydroxyl group
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2013.02.023openalex-snapshot
On the polarity of partially fluorinated methyl groups
inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2016.11.026openalex-snapshot
Biophysical characterization and antineoplastic activity of new bis(thiosemicarbazonato) Cu(II) complexes
inferred← citeshttps://doi.org/10.1016/j.mencom.2019.05.029openalex-snapshot
The efficient synthesis of 3-hydroxyoxetane-3-carboxamides by the reaction of carbamoylsilanes with oxetan-3-one
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.147461openalex-snapshot
Morpholine-Appended 1,8-Naphthalimide Derivatives: Synthesis, DNA Binding, Computational Insight, and in vitro Cytotoxicity
inferred← citeshttps://doi.org/10.1016/j.orgel.2023.106987openalex-snapshot
3-oxetanylmethanol as additive to PEDOT:PSS for improved conductivity and water-resistance and applications in ink-jet printed electrochemical transistors
inferred← citeshttps://doi.org/10.1016/j.talanta.2025.129074openalex-snapshot
Paternò-Büchi reaction-mediated high-selectivity screening of isoprene-containing naturals by LC-HRMS
inferred← citeshttps://doi.org/10.1016/j.tchem.2026.100153openalex-snapshot
Recent advances in the late-stage modification of complex bioactive molecules with oxetanes and azetidines
inferred← citeshttps://doi.org/10.1016/j.tet.2013.02.065openalex-snapshot
Synthesis of 1,5-diazaspiro[2.3]hexanes, a novel diazaspirocyclic system
inferred← citeshttps://doi.org/10.1016/j.tet.2013.03.067openalex-snapshot
Synthesis of 2- and 3-trifluoromethylmorpholines: useful building blocks for drug discovery
inferred← citeshttps://doi.org/10.1016/j.tet.2013.03.072openalex-snapshot
1-Amino-4,4-difluorocyclohexanecarboxylic acid as a promising building block for drug discovery: design, synthesis and characterization
inferred← citeshttps://doi.org/10.1016/j.tet.2015.07.016openalex-snapshot
Efficient one-pot synthesis of dihydroquinolinones in water at room temperature
inferred← citeshttps://doi.org/10.1016/j.tet.2016.03.078openalex-snapshot
Synthesis of oxetane-3-carboxaldehyde and methyl oxetane-3-carboxylate via homologation of oxetane-3-one
inferred← citeshttps://doi.org/10.1016/j.tet.2018.02.001openalex-snapshot
The C4-functionalized 9,10-seco-5,7,10(19)-cholestatriene derivatives: Concise synthesis and characterization of novel vitamin D analogues with a four-membered heterocyclic ether
inferred← citeshttps://doi.org/10.1016/j.tet.2018.02.069openalex-snapshot
Oxetane ethers are formed reversibly in the lithium-catalyzed Friedel–Crafts alkylation of phenols with oxetanols: Synthesis of dihydrobenzofurans, diaryloxetanes, and oxetane ethers
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133552openalex-snapshot
Synthesis of cyclobutyl-fused tetralones via photolytic [2+2] Cycloaddition
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134468openalex-snapshot
Spiro-heterocycles: Recent advances in biological applications and synthetic strategies
inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.08.017openalex-snapshot
Determination of the absolute configuration of two αvβ6 integrin inhibitors for the treatment of idiopathic pulmonary fibrosis and investigations on the asymmetric 1,4-addition of arylboronic acids to crotonate esters bearing a C4-oxygen substituent
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.11.118openalex-snapshot
Synthesis of 3,3-disubstituted oxetane building blocks
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.04.054openalex-snapshot
An improved synthesis of 2-oxa-7-azaspiro[3,5]nonane and analogs as novel reagents in medicinal chemistry
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.07.017openalex-snapshot
Synthesis of (±)-6-oxa-3-azabicyclo[3.1.1]heptan-2-thione: a potential synthon for the preparation of novel heteroaryl-annulated bicyclic morpholines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.01.010openalex-snapshot
Evaluation of a flow-photochemistry platform for the synthesis of compact modules
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.03.065openalex-snapshot
Passerini reactions for the efficient synthesis of 3,3-disubstituted oxetanes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.06.105openalex-snapshot
Trifluoroacetic anhydride—catalyzed conjugate addition of boronic acids to α,β-unsaturated ketones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.03.139openalex-snapshot
Synthesis and cycloaddition chemistry of oxetanyl-substituted sydnones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.08.074openalex-snapshot
FeCl 3 /pyridine: dual-activation in opening of epoxide with carboxylic acid under solvent free condition
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.11.077openalex-snapshot
Pictet–Spengler reactions of oxetan-3-ones and related heterocycles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.05.060openalex-snapshot
Concise synthesis and characterization of novel seco-steroids bearing a spiro-oxetane instead of a metabolically labile C3-hydroxy group
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.06.024openalex-snapshot
A new and versatile synthesis of 3-substituted oxetan-3-yl methyl alcohols
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.12.097openalex-snapshot
Synthesis of novel and conformationally constrained bridged amino acids as compact modules for drug discovery
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.05.053openalex-snapshot
Synthesis of oxetane/azetidine containing spirocycles via the 1,3-dipolar cycloaddition reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.12.054openalex-snapshot
Synthesis of aminobenzoxazoles via simple, clean and efficient electrochemical redox reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152600openalex-snapshot
An efficient and flexible route to novel triazolopiperazine scaffolds
inferred← citeshttps://doi.org/10.1016/j.xcrp.2024.102230openalex-snapshot
Radical electrophilic aromatic substitution of electron-deficient aryl halides via aerobic ternary electron donor-acceptor photocatalysis
inferred← citeshttps://doi.org/10.1021/acs.accounts.0c00814openalex-snapshot
Discovery and Surprises with Cyclizations, Cycloadditions, Fragmentations, and Rearrangements in Complex Settings
inferred← citeshttps://doi.org/10.1021/acs.chemrev.1c00416openalex-snapshot
Photocatalysis in the Life Science Industry
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00274openalex-snapshot
Oxetanes: Recent Advances in Synthesis, Reactivity, and Medicinal Chemistry
inferred← citeshttps://doi.org/10.1021/acs.chemrev.9b00155openalex-snapshot
A Million Crystal Structures: The Whole Is Greater than the Sum of Its Parts
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.0c00478openalex-snapshot
4-Acyl Pyrroles as Dual BET-BRD7/9 Bromodomain Inhibitors Address BETi Insensitive Human Cancer Cell Lines
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.0c00530openalex-snapshot
Amide Bond Bioisosteres: Strategies, Synthesis, and Successes
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