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Electrochemical Selenation/Cyclization of Quinones: A Rapid, Green and Efficient Access to Functionalized Trypanocidal and Antitumor Compounds

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Copper‐Catalyzed C(sp2)–C(sp3) Cross‐Dehydrogenative Coupling of Quinones with Cyclic Alkanes: One‐Step Access to Parvaquone and its Analogs
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Organocatalytic Highly Enantioselective α‐Arylation of β‐Ketoesters
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Asymmetric Organocatalytic α‐Arylation of Aldehydes
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Electrochemical C−H/N−H Activation by Water‐Tolerant Cobalt Catalysis at Room Temperature
inferredcites →https://doi.org/10.1002/anie.200701009openalex-snapshot
Organocatalytic Highly Enantioselective α‐Arylation of β‐Ketoesters
inferredcites →https://doi.org/10.1002/anie.200701207openalex-snapshot
Asymmetric Organocatalytic α‐Arylation of Aldehydes
inferredcites →https://doi.org/10.1002/anie.201712647openalex-snapshot
Electrochemical C−H/N−H Activation by Water‐Tolerant Cobalt Catalysis at Room Temperature
inferredcites →https://doi.org/10.1002/chem.201000884openalex-snapshot
Selenium‐ and Tellurium‐Containing Multifunctional Redox Agents as Biochemical Redox Modulators with Selective Cytotoxicity
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Electrochemical Transition‐Metal‐Catalyzed C−H Bond Functionalization: Electricity as Clean Surrogates of Chemical Oxidants
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Cobaltaelectro‐Catalyzed C−H Activation with Carbon Monoxide or Isocyanides
inferredcites →https://doi.org/10.1002/ejoc.201001570openalex-snapshot
Organocatalytic Michael Addition of Naphthoquinone with α,β‐Unsaturated Ketones: Primary Amine Catalyzed Asymmetric Synthesis of Lapachol Analogues
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Synthesis of 2,3‐Disubstituted 1,4‐Naphthoquinones via Metal‐Free C(sp2)‐H Functionalization Followed by Suzuki Cross‐Coupling Reactions
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Anodic oxidation of diphenyldiselenide in acetonitrile
inferredcites →https://doi.org/10.1016/0022-1759(83)90303-4openalex-snapshot
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
inferredcites →https://doi.org/10.1016/b978-0-12-689650-3.x5001-4openalex-snapshot
Naturally Occurring Quinones
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Naphthoquinoidal [1,2,3]-triazole, a new structural moiety active against Trypanosoma cruzi
inferredcites →https://doi.org/10.1016/j.ejmech.2015.06.044openalex-snapshot
Hybrid compounds with two redox centres: Modular synthesis of chalcogen-containing lapachones and studies on their antitumor activity
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Combinatorial synthesis, in silico , molecular and biochemical studies of tetrazole-derived organic selenides with increased selectivity against hepatocellular carcinoma
inferredcites →https://doi.org/10.1016/j.ejmech.2016.06.019openalex-snapshot
Synthesis and antitumor activity of selenium-containing quinone-based triazoles possessing two redox centres, and their mechanistic insights
inferredcites →https://doi.org/10.1016/j.ejmech.2018.06.040openalex-snapshot
Current advances in drug discovery for Chagas disease
inferredcites →https://doi.org/10.1016/j.ejmech.2019.06.056openalex-snapshot
Synthesis of quinones with highlighted biological applications: A critical update on the strategies towards bioactive compounds with emphasis on lapachones
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2018.11.012openalex-snapshot
Mitochondrial disfunction and ROS production are essential for anti-Trypanosoma cruzi activity of β-lapachone-derived naphthoimidazoles
inferredcites →https://doi.org/10.1016/j.jchromb.2019.04.029openalex-snapshot
UPLC-HRMS and NMR applied in the evaluation of solid-phase extraction methods as a rational strategy of dereplication of Phyllanthus spp. aiming at the discovery of cytotoxic metabolites
inferredcites →https://doi.org/10.1016/j.tetlet.2018.08.052openalex-snapshot
Tetrabutylammonium iodide catalyzed hydroxylation of naphthoquinone derivatives with tert-butyl hydroperoxide as an oxidant
inferredcites →https://doi.org/10.1016/s0022-0728(96)04955-8openalex-snapshot
Electrochemistry and metal complex formation of organic diselenides
inferredcites →https://doi.org/10.1016/s0968-0896(03)00226-8openalex-snapshot
Potent antitumor activity of synthetic 1,2-Naphthoquinones and 1,4-Naphthoquinones
inferredcites →https://doi.org/10.1021/acs.joc.5b02903openalex-snapshot
Kinetic Control of Rh(III)-Catalyzed Annulation of C–H Bonds with Quinones: Chemoselective Synthesis of Hydrophenanthridinones and Phenanthridinones
inferredcites →https://doi.org/10.1021/acs.joc.8b02961openalex-snapshot
Activated Carbon-Promoted Dehydrogenation of Hydroquinones to Benzoquinones, Naphthoquinones, and Anthraquinones under Molecular Oxygen Atmosphere
inferredcites →https://doi.org/10.1021/acs.joc.9b01898openalex-snapshot
1-Methyl-1,4-cyclohexadiene as a Traceless Reducing Agent for the Synthesis of Catechols and Hydroquinones
inferredcites →https://doi.org/10.1021/acs.orglett.5b01974openalex-snapshot
Ir(III)-Catalyzed Oxidative Coupling of NH Isoquinolones with Benzoquinone
inferredcites →https://doi.org/10.1021/acs.orglett.6b01073openalex-snapshot
Ru-Catalyzed Asymmetric Hydrogenative/Transfer Hydrogenative Desymmetrization of Meso-Epoxy Diketones
inferredcites →https://doi.org/10.1021/acs.orglett.6b01586openalex-snapshot
Rh-Catalyzed Reactions of 1,4-Benzoquinones with Electrophiles: C–H Iodination, Bromination, and Phenylselenation
inferredcites →https://doi.org/10.1021/acs.orglett.6b03735openalex-snapshot
Transition-Metal-Free Selective Oxidative C(sp 3 )–S/Se Coupling of Oxindoles, Tetralone, and Arylacetamides: Synthesis of Unsymmetrical Organochalcogenides
inferredcites →https://doi.org/10.1021/acs.orglett.8b02988openalex-snapshot
Metal-, Photocatalyst-, and Light-Free, Late-Stage C–H Alkylation of Heteroarenes and 1,4-Quinones Using Carboxylic Acids
inferredcites →https://doi.org/10.1021/acs.orglett.8b03274openalex-snapshot
Electrochemical Aminoselenation and Oxyselenation of Styrenes with Hydrogen Evolution
inferredcites →https://doi.org/10.1021/acs.orglett.9b00361openalex-snapshot
Catalyst-Free, Direct Electrochemical Tri- and Difluoroalkylation/Cyclization: Access to Functionalized Oxindoles and Quinolinones
inferredcites →https://doi.org/10.1021/acscatal.8b01236openalex-snapshot
Mechanistic Studies on the Anodic Functionalization of Alkenes Catalyzed by Diselenides
inferredcites →https://doi.org/10.1021/acscatal.8b01697openalex-snapshot
Recent Advances in C–H Functionalization Using Electrochemical Transition Metal Catalysis
inferredcites →https://doi.org/10.1021/acscatal.9b02348openalex-snapshot
Cupraelectro-Catalyzed Alkyne Annulation: Evidence for Distinct C–H Alkynylation and Decarboxylative C–H/C–C Manifolds
inferredcites →https://doi.org/10.1021/ja00852a019openalex-snapshot
Organoselenium chemistry. Conversion of ketones to enones by selenoxide syn elimination
inferredcites →https://doi.org/10.1021/ja01190a005openalex-snapshot
Naphthoquinone Antimalarials. XII. The Hooker Oxidation Reaction1
inferredcites →https://doi.org/10.1021/ja01690a026openalex-snapshot
THE ALKYLATION OF HYDROXYNAPHTHOQUINONE I. ORTHO-ETHERS
inferredcites →https://doi.org/10.1021/ja111152zopenalex-snapshot
Practical C−H Functionalization of Quinones with Boronic Acids
inferredcites →https://doi.org/10.1021/ja904380qopenalex-snapshot
Isoquinoline Synthesis via Rhodium-Catalyzed Oxidative Cross-Coupling/Cyclization of Aryl Aldimines and Alkynes
inferredcites →https://doi.org/10.1021/jacs.7b11025openalex-snapshot
Electrochemical Cobalt-Catalyzed C–H Oxygenation at Room Temperature
inferredcites →https://doi.org/10.1021/jacs.8b13371openalex-snapshot
Electrochemical Dearomative 2,3-Difunctionalization of Indoles
inferredcites →https://doi.org/10.1021/jacs.9b07763openalex-snapshot
Flow Rhodaelectro-Catalyzed Alkyne Annulations by Versatile C–H Activation: Mechanistic Support for Rhodium(III/IV)
inferredcites →https://doi.org/10.1021/jo302480jopenalex-snapshot
Transition-Metal-Free Synthesis of Unsymmetrical Diaryl Chalcogenides from Arenes and Diaryl Dichalcogenides
inferredcites →https://doi.org/10.1021/jo501419sopenalex-snapshot
Substituent-Enabled Oxidative Dehydrogenative Cross-Coupling of 1,4-Naphthoquinones with Alkenes
inferredcites →https://doi.org/10.1021/jo502621aopenalex-snapshot
Catalytic Chalcogenylation under Greener Conditions: A Solvent-Free Sulfur- and Seleno-functionalization of Olefins via I2/DMSO Oxidant System
inferredcites →https://doi.org/10.1021/ol402229mopenalex-snapshot
γ-Carbonyl Quinones: Radical Strategy for the Synthesis of Evelynin and Its Analogues by C–H Activation of Quinones Using Cyclopropanols
inferredcites →https://doi.org/10.1021/tx200180yopenalex-snapshot
Preclinical Genotoxicology of Nor-β-lapachone in Human Cultured Lymphocytes and Chinese Hamster Lung Fibroblasts
inferredcites →https://doi.org/10.1021/tx7002257openalex-snapshot
Quinone Formation as a Chemoprevention Strategy for Hybrid Drugs: Balancing Cytotoxicity and Cytoprotection
inferredcites →https://doi.org/10.1039/a804287jopenalex-snapshot
Pyranonaphthoquinone antibiotics—isolation, structure and biological activity
inferredcites →https://doi.org/10.1039/b107972gopenalex-snapshot
Electrochemistry of chalcogen compounds: prediction of antioxidant activity.
inferredcites →https://doi.org/10.1039/b802259nopenalex-snapshot
Dialkyl dichalcogen cations
inferredcites →https://doi.org/10.1039/b823149dopenalex-snapshot
Multicomponent reactions for the synthesis of multifunctional agents with activity against cancer cells
inferredcites →https://doi.org/10.1039/b907831bopenalex-snapshot
Exploring synthetic avenues for the effective synthesis of selenium- and tellurium-containing multifunctional redox agents
inferredcites →https://doi.org/10.1039/c2cc30931aopenalex-snapshot
An organocatalytic Michael-aldol cascade: formal [3+2] annulation to construct enantioenriched spirocyclic oxindole derivatives
inferredcites →https://doi.org/10.1039/c4np00127copenalex-snapshot
Naphthopyranones – isolation, bioactivity, biosynthesis and synthesis
inferredcites →https://doi.org/10.1039/c4ob02624aopenalex-snapshot
Rh( iii )-catalyzed direct C–H/C–H cross-coupling of quinones with arenes assisted by a directing group: identification of carbazole quinones as GSKβ inhibitors
inferredcites →https://doi.org/10.1039/c5ra16213kopenalex-snapshot
On the investigation of hybrid quinones: synthesis, electrochemical studies and evaluation of trypanocidal activity
inferredcites →https://doi.org/10.1039/c6ob01119eopenalex-snapshot
Catalytic asymmetric reactions and synthesis of quinones
inferredcites →https://doi.org/10.1039/c6ob01856dopenalex-snapshot
Regioselective transition metal- and halogen-free direct dithiolation at C(sp 3 )–H of nitrotoluenes with diaryl disulfides
inferredcites →https://doi.org/10.1039/c6sc00302hopenalex-snapshot
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C–H iodination as a gateway to functionalized derivatives
inferredcites →https://doi.org/10.1039/c7cs00553aopenalex-snapshot
Quinone-based fluorophores for imaging biological processes
inferredcites →https://doi.org/10.1039/c7cs00619eopenalex-snapshot
Electrochemical strategies for C–H functionalization and C–N bond formation
inferredcites →https://doi.org/10.1039/c8cc03147aopenalex-snapshot
Weakly-coordinating N -oxide and carbonyl groups for metal-catalyzed C–H activation: the case of A-ring functionalization
inferredcites →https://doi.org/10.1039/c8cc08768gopenalex-snapshot
Electrochemical benzylic oxidation of C–H bonds
inferredcites →https://doi.org/10.1039/c8ob00196kopenalex-snapshot
Direct sequential C–H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones
inferredcites →https://doi.org/10.1039/c9cc04203bopenalex-snapshot
2-Iodoxybenzoic acid ditriflate: the most powerful hypervalent iodine( v ) oxidant
inferredcites →https://doi.org/10.1039/c9nj02026hopenalex-snapshot
Copper complexes and carbon nanotube–copper ferrite-catalyzed benzenoid A-ring selenation of quinones: an efficient method for the synthesis of trypanocidal agents
inferredcites →https://doi.org/10.1039/c9qo01005jopenalex-snapshot
Clavipines A–C, antiproliferative meroterpenoids with a fused azepine skeleton from the basidiomycete Clitocybe clavipes
inferredcites →https://doi.org/10.1039/c9sc02289aopenalex-snapshot
Total synthesis of griseusins and elucidation of the griseusin mechanism of action
inferredcites →https://doi.org/10.1055/s-0037-1611568openalex-snapshot
Metallaelectro-Catalyzed C–H Activation by Weak Coordination
inferredcites →https://doi.org/10.1055/s-0037-1612080openalex-snapshot
A Copper Halide Promoted Regioselective Halogenation of Coumarins Using N-Halosuccinimide as Halide Source
inferredcites →https://doi.org/10.1056/nejmoa1507574openalex-snapshot
Randomized Trial of Benznidazole for Chronic Chagas’ Cardiomyopathy
inferredcites →https://doi.org/10.1128/aac.01241-09openalex-snapshot
In Vitro and In Vivo Activities of 1,3,4-Thiadiazole-2-Arylhydrazone Derivatives of Megazol against Trypanosoma cruzi
inferredcites →https://doi.org/10.1590/s0100-879x2002000700008openalex-snapshot
In vitro antimicrobial activity of a new series of 1,4-naphthoquinones
inferredcites →https://doi.org/10.2174/1385272821666170126171927openalex-snapshot
Natural Quinones: Antioxidant and Antiaggregant Action Towards Glyceraldehyde-3-Phosphate Dehydrogenase
inferredcites →https://doi.org/10.2174/1568026616666161025161858openalex-snapshot
Clear Shot at Primary Aim: Susceptibility of Trypanosoma cruzi Organelles, Structures and Molecular Targets to Drug Treatment
inferredcites →https://doi.org/10.3389/fchem.2018.00339openalex-snapshot
Quinone-Derived π-Extended Phenazines as New Fluorogenic Probes for Live-Cell Imaging of Lipid Droplets
inferredcites →https://doi.org/10.3390/antiox6020038openalex-snapshot
The Reactive Sulfur Species Concept: 15 Years On

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Electrochemical Sulphenylation/Cyclization of Quinones: A Rapid, Green, and Efficient Access to Cytotoxic Compounds
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Direct Functionalization of para‐Quinones: A Historical Review and New Perspectives
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High-yielding regioselective synthesis of p -quinone fused 5-substituted-1,4-benzodiazepine scaffolds via Pictet–Spengler type cycloannulation
inferred← citeshttps://doi.org/10.1039/d4ra02812kopenalex-snapshot
Green advancements towards the electrochemical synthesis of heterocycles
inferred← citeshttps://doi.org/10.1039/d6qo00817hopenalex-snapshot
Forging potent trypanocidal quinones via aryne chemistry: from naphthoquinonynes to selenium- and tellurium-embedded redox scaffolds
inferred← citeshttps://doi.org/10.1055/a-2169-3807openalex-snapshot
Recent Advances in Electrochemically Mediated Reactions of Diselenides
inferred← citeshttps://doi.org/10.1055/a-2184-8411openalex-snapshot
Electrochemical Synthesis of Organoselenium Compounds: A Graphical Review
inferred← citeshttps://doi.org/10.1055/s-0043-1775373openalex-snapshot
A Practical Electrochemical Approach for Synthesizing Selenyl-Dihydrobenzofurans and Chromane with a Tetrasubstituted Carbon Center
inferred← citeshttps://doi.org/10.1111/cbdd.14122openalex-snapshot
Natural naphthoquinones and their derivatives as potential drug molecules against trypanosome parasites
inferred← citeshttps://doi.org/10.21203/rs.3.rs-10027778/v1openalex-snapshot
Small-Molecule Mimicry Intercepts PEX5 Recognition by Trypanosomal PEX14 as Revealed by Molecular Dynamics
inferred← citeshttps://doi.org/10.3390/catal13081221openalex-snapshot
Recent Advances in Design and Synthesis of 1,3-Thiaselenolane and 1,3-Thiaselenole Derivatives
inferred← citeshttps://doi.org/10.3390/chemosensors10010019openalex-snapshot
Rational Design and Synthesis of Large Stokes Shift 2,6-Sulphur-Disubstituted BODIPYs for Cell Imaging
inferred← citeshttps://doi.org/10.3390/molecules27051597openalex-snapshot
“Green Is the Color”: An Update on Ecofriendly Aspects of Organoselenium Chemistry
inferred← citeshttps://doi.org/10.3390/molecules28052206openalex-snapshot
Electro-Oxidative C3-Selenylation of Pyrido[1,2-a]pyrimidin-4-ones
inferred← citeshttps://doi.org/10.3390/sci7020074openalex-snapshot
The Chalcogen Exchange: The Replacement of Oxygen with Sulfur and Selenium to Boost the Activity of Natural Products
inferred← citeshttps://doi.org/10.6023/cjoc202109046openalex-snapshot
Study on the Application of Photoelectric Technology in the Synthesis of Selenium-Containing Heterocycles
inferred← citeshttps://doi.org/10.6023/cjoc202204066openalex-snapshot
Recent Progress on the Electrochemical Difunctionalization of Alkenes/Alkynes
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