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Oxidative Dimerization of (E)- and (Z)-2-Propenylsesamol with O2 in the Presence and Absence of Laccases and Other Catalysts: Selective Formation of Carpanones and Benzopyrans under Different Reaction Conditions
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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/(sici)1521-3773(19980302)37:4<388::aid-anie388>3.0.co;2-vopenalex-snapshot
The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon Stereocenters
inferredcites →https://doi.org/10.1002/1521-3773(20020517)41:10<1650::aid-anie1650>3.0.co;2-bopenalex-snapshot
Catalytic Enantioselective Diels-Alder Reactions: Methods, Mechanistic Fundamentals, Pathways, and Applications
inferredcites →https://doi.org/10.1002/1521-3773(20020517)41:10<1668::aid-anie1668>3.0.co;2-zopenalex-snapshot
The Diels-Alder Reaction in Total Synthesis
inferredcites →https://doi.org/10.1002/9783527609925openalex-snapshot
Domino Reactions in Organic Synthesis
inferredcites →https://doi.org/10.1002/adsc.200700043openalex-snapshot
Laccase‐Catalyzed Dimerization of Hydroxystilbenes
inferredcites →https://doi.org/10.1002/adsc.200800775openalex-snapshot
Synthetic Applications of Laccase in Green Chemistry
inferredcites →https://doi.org/10.1002/anie.197700101openalex-snapshot
Intramolecular [4+2] and [3+2] Cycloadditions in Organic Synthesis
inferredcites →https://doi.org/10.1002/anie.200200534openalex-snapshot
Chemistry and Biology of Biosynthetic Diels–Alder Reactions
inferredcites →https://doi.org/10.1002/anie.200904622openalex-snapshot
An Enantiocomplementary Dirigent Protein for the Enantioselective Laccase‐Catalyzed Oxidative Coupling of Phenols
inferredcites →https://doi.org/10.1002/bit.10681openalex-snapshot
Combined sequence and structure analysis of the fungal laccase family
inferredcites →https://doi.org/10.1002/jhet.232openalex-snapshot
Syntheses of chromenes and chromanes via o‐quinone methide intermediates
inferredcites →https://doi.org/10.1006/bbrc.2001.5593openalex-snapshot
Polymerization of Bisphenol A by Purified Laccase from Trametes villosa
inferredcites →https://doi.org/10.1007/bf00425105openalex-snapshot
The importance of phenol oxidase activity in lignin degradation by the white-rot fungus Sporotrichum pulverulentum
inferredcites →https://doi.org/10.1007/s00203-002-0510-7openalex-snapshot
Laccases and their occurrence in prokaryotes
inferredcites →https://doi.org/10.1007/s00253-009-1869-zopenalex-snapshot
Fungal laccases as tools for the synthesis of new hybrid molecules and biomaterials
inferredcites →https://doi.org/10.1007/s002530000590openalex-snapshot
Modification of lignin for the production of new compounded materials
inferredcites →https://doi.org/10.1016/0022-2364(71)90082-5openalex-snapshot
NMR spectra of symmetric molecules. I. The spin Hamiltonian for twofold symmetry
inferredcites →https://doi.org/10.1016/1381-1169(95)00251-0openalex-snapshot
A novel method for conversion of benzyl alcohols to benzaldehydes by laccase-catalysed oxidation
inferredcites →https://doi.org/10.1016/j.abb.2008.03.009openalex-snapshot
Comparative characterization of four laccases from Trametes versicolor concerning phenolic C–C coupling and oxidation of PAHs
inferredcites →https://doi.org/10.1016/j.biotechadv.2006.04.003openalex-snapshot
Industrial and biotechnological applications of laccases: A review
inferredcites →https://doi.org/10.1016/j.femsle.2005.01.054openalex-snapshot
Phylogenetic and biochemical characterisation of a recombinant laccase fromTrametes versicolor
inferredcites →https://doi.org/10.1016/j.intimp.2010.06.001openalex-snapshot
Sauchinone, a lignan from Saururus chinensis, reduces tumor necrosis factor-α production through the inhibition of c-raf/MEK1/2/ERK 1/2 pathway activation
inferredcites →https://doi.org/10.1016/j.tet.2003.10.117openalex-snapshot
Biotransformation of resveratrol: synthesis of trans-dehydrodimers catalyzed by laccases from Myceliophtora thermophyla and from Trametes pubescens
inferredcites →https://doi.org/10.1016/j.tet.2005.12.076openalex-snapshot
Comparison of TEMPO and its derivatives as mediators in laccase catalysed oxidation of alcohols
inferredcites →https://doi.org/10.1016/j.tetasy.2004.06.034openalex-snapshot
Laccase-mediated oxidation of the steroid hormone 17β-estradiol in organic solvents
inferredcites →https://doi.org/10.1016/j.tetlet.2007.05.089openalex-snapshot
Laccase initiated oxidative domino reactions for the efficient synthesis of 3,4-dihydro-7,8-dihydroxy-2H-dibenzofuran-1-ones
inferredcites →https://doi.org/10.1016/j.tetlet.2009.04.043openalex-snapshot
Total synthesis of polemannones B and C
inferredcites →https://doi.org/10.1016/j.tibtech.2006.03.006openalex-snapshot
Laccases: blue enzymes for green chemistry
inferredcites →https://doi.org/10.1016/s0031-9422(00)84743-3openalex-snapshot
Benzoxanthenone derivatives from Polemannia montana
inferredcites →https://doi.org/10.1016/s0031-9422(02)00171-1openalex-snapshot
Laccase: new functions for an old enzyme
inferredcites →https://doi.org/10.1016/s0040-4020(00)00949-2openalex-snapshot
Oxidative conjugation of catechols with proteins in insect skeletal systems
inferredcites →https://doi.org/10.1016/s0040-4020(02)00496-9openalex-snapshot
o-Quinone methides: intermediates underdeveloped and underutilized in organic synthesis
inferredcites →https://doi.org/10.1016/s0040-4039(01)82977-4openalex-snapshot
Transition metal(ii) schiff's base complexes catalyzed oxidation of trans-2-(1-propenyl)-4,5-methylenedioxyphenol to carpanone by molecular oxygen
inferredcites →https://doi.org/10.1016/s0040-4039(01)88911-5openalex-snapshot
Novel lignans from a sp. from bougainville
inferredcites →https://doi.org/10.1016/s0040-4039(03)00902-xopenalex-snapshot
Synthesis of coumarins by ring-closing metathesis using Grubbs’ catalyst
inferredcites →https://doi.org/10.1016/s0040-4039(98)01215-5openalex-snapshot
Synthesis of aromatic aldehydes by laccase-mediator assisted oxidation
inferredcites →https://doi.org/10.1016/s0141-0229(02)00214-4openalex-snapshot
Applications of laccases and tyrosinases (phenoloxidases) immobilized on different supports: a review
inferredcites →https://doi.org/10.1016/s1381-1177(00)00184-3openalex-snapshot
Oxidation of isoeugenol and coniferyl alcohol catalyzed by laccases isolated from Rhus vernicifera Stokes and Pycnoporus coccineus
inferredcites →https://doi.org/10.1021/cr100334xopenalex-snapshot
Redox Reactions Catalyzed by Isolated Enzymes
inferredcites →https://doi.org/10.1021/ja056338gopenalex-snapshot
Synthesis of a 10,000-Membered Library of Molecules Resembling Carpanone and Discovery of Vesicular Traffic Inhibitors
inferredcites →https://doi.org/10.1021/ja0585533openalex-snapshot
Palladium(II)-Catalyzed Aerobic Hydroalkoxylation of Styrenes Containing a Phenol
inferredcites →https://doi.org/10.1021/ja993674mopenalex-snapshot
Solid-Phase Biomimetic Synthesis of Carpanone-like Molecules
inferredcites →https://doi.org/10.1021/jf60059a002openalex-snapshot
Insecticide Synergists, 3,4-Methylenedioxyphenoxy Compounds as Synergists for Natural and Synthetic Pyrethrins
inferredcites →https://doi.org/10.1021/jo01092a029openalex-snapshot
Synthesis of Methylenedioxyphenyl Compounds from Isosafrole and Sesamol
inferredcites →https://doi.org/10.1021/jo201789kopenalex-snapshot
Applications of ortho-Quinone Methide Intermediates in Catalysis and Asymmetric Synthesis
inferredcites →https://doi.org/10.1021/jo202082vopenalex-snapshot
Laccase-Catalyzed Domino Reactions between Hydroquinones and Cyclic 1,3-Dicarbonyls for the Regioselective Synthesis of Substitutedp-Benzoquinones
inferredcites →https://doi.org/10.1021/jo9011915openalex-snapshot
The Laccase-Catalyzed Domino Reaction between Catechols and Heterocyclic 1,3-Dicarbonyls and the Unambiguous Structure Elucidation of the Products by NMR Spectroscopy and X-ray Crystal Structure Analysis
inferredcites →https://doi.org/10.1021/np990499eopenalex-snapshot
Hepatoprotective Diastereomeric Lignans from Saururus chinensis Herbs
inferredcites →https://doi.org/10.1021/ol801643topenalex-snapshot
A New Catalytic Cu(II)/Sparteine Oxidant System for β,β-Phenolic Couplings of Styrenyl Phenols: Synthesis of Carpanone and Unnatural Analogs
inferredcites →https://doi.org/10.1021/ol9017326openalex-snapshot
A New Cross-Coupling-Based Synthesis of Carpanone
inferredcites →https://doi.org/10.1039/b203388gopenalex-snapshot
A concise synthesis of carpanone using solid-supported reagents and scavengers
inferredcites →https://doi.org/10.1039/b210978fopenalex-snapshot
A study of the oxidation of ethers with the enzyme laccase under mediation by two N–OH–type compounds
inferredcites →https://doi.org/10.1039/b507657aopenalex-snapshot
New mediators for the enzyme laccase: mechanistic features and selectivity in the oxidation of non-phenolic substrates
inferredcites →https://doi.org/10.1039/b800799copenalex-snapshot
O2 Reduction to H2O by the multicopper oxidases
inferredcites →https://doi.org/10.1039/b822977eopenalex-snapshot
Combined action of enzymes: the first domino reaction catalyzed by Agaricus bisporus
inferredcites →https://doi.org/10.1039/c1ob00012hopenalex-snapshot
Laccase-catalyzed phenol oxidation. Rapid assignment of ring-proton deficient polycyclic benzofuran regioisomers by experimental 1H–13C long-range coupling constants and DFT-predicted product formation
inferredcites →https://doi.org/10.1042/bj2680475openalex-snapshot
Comparison of lignin peroxidase, horseradish peroxidase and laccase in the oxidation of methoxybenzenes
inferredcites →https://doi.org/10.1042/bst0340304openalex-snapshot
Green oxidations with laccase–mediator systems
inferredcites →https://doi.org/10.1055/s-2001-16783openalex-snapshot
A Concise Synthesis of the Natural Product Carpanone Using Solid-Supported Reagents and Scavengers
inferredcites →https://doi.org/10.1055/s-2007-981525openalex-snapshot
Immunosuppressive Lignans Isolated from Saururus chinensis
inferredcites →https://doi.org/10.1071/ch9691803openalex-snapshot
trans -2-Methoxy-4,5-methylenedioxypropenylbenzene (carpacin) from a Cinnamomum sp. from Bougainville
inferredcites →https://doi.org/10.1099/13500872-140-1-19openalex-snapshot
The structure and function of fungal laccases
inferredcites →https://doi.org/10.1104/pp.010988openalex-snapshot
Laccase Down-Regulation Causes Alterations in Phenolic Metabolism and Cell Wall Structure in Poplar
inferredcites →https://doi.org/10.1104/pp.99.3.1162openalex-snapshot
Laccase from Sycamore Maple (Acer pseudoplatanus) Polymerizes Monolignols
inferredcites →https://doi.org/10.1111/j.1574-6968.1993.tb06100.xopenalex-snapshot
Polyphenol oxidase inAzospirillum lipoferumisolated from rice rhizosphere: Evidence for laccase activity in non-motile strains ofAzospirillum lipoferum
inferredcites →https://doi.org/10.1126/science.260.5108.672openalex-snapshot
A Laccase Associated with Lignification in Loblolly Pine Xylem
inferredcites →https://doi.org/10.1246/bcsj.65.1662openalex-snapshot
Silver(I) Oxide Catalyzed Oxidation of o-Allyl- and o-(1-Propenyl)phenols
inferredcites →https://doi.org/10.3987/com-95-7370openalex-snapshot
Studies of Constituents of Saururus chinensis
inferredcites →https://doi.org/10.7164/antibiotics.46.141openalex-snapshot
Enzymatic dimerization of penicillin X.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4666804openalex-extracted
Inverse Electron Demand Diels-Alder Reaction in Total Synthesis of Bioactive Natural Products
inferred← citeshttps://doi.org/10.1002/047084289x.rn01457.pub2openalex-snapshot
Cyclohexanediylbis(nitrilomethylidyne)]bis[4,6‐bis(1,1‐dimethylethyl)‐phenolato]](2‐)‐ N , N ′ , O , O ′ ]‐,[SP‐4‐2‐(1 R ‐ trans )]‐; N , N ′ ‐bis(3,5‐di‐ tert ‐butylsalicylidene)‐1,2‐diaminocyclohexanecobalt(II)
inferred← citeshttps://doi.org/10.1002/9783527671304.ch5openalex-snapshot
Radical Reactions in Domino Processes
inferred← citeshttps://doi.org/10.1002/adsc.201300960openalex-snapshot
Laccase and Laccase‐Mediated Systems in the Synthesis of Organic Compounds
inferred← citeshttps://doi.org/10.1002/asia.201901727openalex-snapshot
Diastereoselective Synthesis of Benzoxanthenones
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Antioxidant Chemistry of Phenolics in Chinese Herbal Medicines: A Holism‐Based Review
inferred← citeshttps://doi.org/10.1002/cctc.201200266openalex-snapshot
Selective Catalytic Oxidation of CH Bonds with Molecular Oxygen
inferred← citeshttps://doi.org/10.1007/978-3-032-09901-3_1openalex-snapshot
The Diels–Alder Reaction as a Key Step in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1007/s11172-014-0688-2openalex-snapshot
Spatial structure of 2-(2´-hydroxyphenyl)-4-methylchromanes and some specific features of intramolecular hydrogen bond
inferred← citeshttps://doi.org/10.1016/b978-0-12-812823-7.00318-9openalex-snapshot
Solutions 251 – 300
inferred← citeshttps://doi.org/10.1016/j.procbio.2015.05.011openalex-snapshot
Laccase initiated C C couplings: Various techniques for reaction monitoring
inferred← citeshttps://doi.org/10.1016/j.tchem.2024.100066openalex-snapshot
Inverse electron demand Diels-Alder reaction in total synthesis of bioactive natural products
inferred← citeshttps://doi.org/10.1016/j.tet.2013.03.023openalex-snapshot
Laccase-catalyzed reaction of 3-tert-butyl-1H-pyrazol-5(4H)-one with substituted catechols using air as an oxidant
inferred← citeshttps://doi.org/10.1016/j.tet.2014.05.043openalex-snapshot
Studies on synthesis of spirolactone annulated bicyclo[2.2.2]octanes: tricyclic core of yaoshanenolides
inferred← citeshttps://doi.org/10.1016/j.tet.2014.08.044openalex-snapshot
Molecular complexity from aromatics. Studies on synthesis of polycyclic system related to crotogoudin
inferred← citeshttps://doi.org/10.1016/j.tet.2014.12.033openalex-snapshot
Molecular diversity from aromatics. Cycloaddition of cyclohexa-2,4-dienones, ring-closing metathesis and sigmatropic shifts: a general and stereoselective route to novel spirocarbocyclics
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Benzofuran as a dienophile in π4s+π2s cycloaddition with cyclohexa-2,4-dienones. Studies on synthesis and photoreaction of dihydrobenzofuran annulated bicyclo[2.2.2]octenones
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Molecular complexity and diversity from aromatics. Intramolecular cycloaddition of cyclohexa-2,4-dienones and sigmatropic shift in excited state: a unified approach towards synthesis of polycyclic frameworks related to crotogoudin, conidiogenol, and crinipellins
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Studies on cycloaddition of spiroepoxycyclohexa-2,4-dienones with indene and sigmatropic shifts in excited states: Synthesis of benzotricyclo[5.2.2.02,6]undec-10-en-9-ones, annulated polyquinanes and bicyclo[4.2.0]octanoids
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131645openalex-snapshot
Chiral vanadium complex-catalyzed oxidative coupling of arenols
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Oxidative dearomatization and unusual intramolecular Diels–Alder reaction of cyclohexa-2,4-dienone: synthesis and photoreaction of oxa-tricyclo[5.2.2.01,5]undec-10-ene-8-ones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.11.119openalex-snapshot
Green and mild laccase-catalyzed aerobic oxidative coupling of benzenediol derivatives with various sodium benzenesulfinates
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Laccase-catalyzed, aerobic oxidative coupling of 4-substituted urazoles with sodium arylsulfinates: Green and mild procedure for the synthesis of arylsulfonyl triazolidinediones
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Oxidative dearomatization and retro-Diels-Alder/Diels-Alder cascade: Synthesis and photoreactions of azepane annulated bicyclo[2.2.2]octenone
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An unexpected Pummerer rearrangement in the synthetic route to ethyl (2′-hydroxy-4′,5′-methylenedioxyphenyl)acetate: An alternative approach to 2,3-dimethylthio benzofurans
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Isomerization of Allylbenzenes
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Enantiomeric Prenylated Neolignans from the Roots of Illicium verum with Analgesic Activity
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Taicrypnacids A and B, a Pair of C37 Heterodimeric Diterpenoid Stereoisomers from Taiwania cryptomerioides
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π4s + π2s Cycloaddition of Spiroepoxycyclohexa-2,4-dienone, Radical Cyclization, and Oxidation–Aldol–Oxidation Cascade: Synthesis of BCDE Ring of Atropurpuran
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Cycloaddition of Spiroepoxycyclohexa-2,4-dienones, Radical Cyclization and 1,3-Acyl Shift in Excited State: Aromatics to Sterpuren-4-one
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01821openalex-snapshot
An Autonomous Self-Optimizing Flow Reactor for the Synthesis of Natural Product Carpanone
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Reconfigurable Flow Platform for Automated Reagent Screening and Autonomous Optimization for Bioinspired Lignans Synthesis
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Comparing Gas–Liquid Segmented and Tube-in-Tube Setups for the Aerobic Dimerization of Desmethoxycarpacine with an Automated Flow Platform
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N-Iodosuccinimide-Mediated Dimerization of 2-Alkynylnaphthols: A Highly Diastereoselective Construction of Bridged Polycyclic Compounds via Vinylidene ortho-Quinone Methide Intermediate
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Selectfluor-Mediated Stereoselective [1 + 1 + 4 + 4] Dimerization of Styrylnaphthols
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Aerobic Oxidative Cascade Reaction of ortho -Alkenylphenols for Asymmetric Synthesis of Benzoxanthenones
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Laccase-catalyzed oxidative phenolic coupling of vanillidene derivatives
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Laccase-catalyzed oxidation of Hantzsch 1,4-dihydropyridines to pyridines and a new one pot synthesis of pyridines
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Synthesis of disulfides by laccase-catalyzed oxidative coupling of heterocyclic thiols
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Laccase-catalyzed synthesis of catechol thioethers by reaction of catechols with thiols using air as an oxidant
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Eugenol isomerization promoted by arene–ruthenium(ii) complexes in aqueous media: influence of the pH on the catalytic activity
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The first enzymatic Achmatowicz reaction: selective laccase-catalyzed synthesis of 6-hydroxy-(2H)-pyran-3(6H)-ones and (2H)-pyran-2,5(6H)-diones
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Laccase-catalyzed green synthesis and cytotoxic activity of novel pyrimidobenzothiazoles and catechol thioethers
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Laccase-mediated synthesis of bioactive natural products and their analogues
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Total syntheses of ericifolione and its analogues via a biomimetic inverse-electron-demand Diels–Alder reaction
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Oxidative dehydrogenative couplings of alkenyl phenols
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Divergent cyclodimerizations of styrylnaphthols under aerobic visible-light irradiation and Brønsted acid catalysis
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3.2.2 Oxidation Other Than with Cytochrome P450s
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7 Enzymatic Oxidative Dearomatization Reactions
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Selection of organic solvents as reaction media for laccase from Trametes versicolor
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Applications of Flow Chemistry in Total Synthesis of Natural Products
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Antifungal Activity against Botrytis cinerea of 2,6-Dimethoxy-4-(phenylimino)cyclohexa-2,5-dienone Derivatives
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Benzoxanthenone Lignans Related to Carpanone, Polemanone, and Sauchinone: Natural Origin, Chemical Syntheses, and Pharmacological Properties
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