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Selenium-Catalyzed Regioselective Cyclization of Unsaturated Carboxylic Acids Using Hypervalent Iodine Oxidants
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Organoselenchemie in der stereoselektiven Synthese
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inferredcites →https://doi.org/10.1002/anie.200702313openalex-snapshot
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inferredcites →https://doi.org/10.1002/anie.200903893openalex-snapshot
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inferredcites →https://doi.org/10.1002/ejoc.201000308openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tetlet.2005.10.055openalex-snapshot
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inferredcites →https://doi.org/10.1039/a909819dopenalex-snapshot
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inferredcites →https://doi.org/10.1039/b913052gopenalex-snapshot
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inferredcites →https://doi.org/10.1055/s-1999-2630openalex-snapshot
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inferredcites →https://doi.org/10.1246/bcsj.75.2233openalex-snapshot
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SeO2/H2O2/H2O-Dioxane: A New Catalytic System for Trans Dihydroxylation of Olefins
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Design and preparation of a polymer resin-supported organoselenium catalyst with industrial potential
inferred← citeshttps://doi.org/10.1039/c9dt00465copenalex-snapshot
Facile synthesis of mixed O, S or Se bearing hexasubstituted benzenes and their potential as Cu( ii ) ion probe
inferred← citeshttps://doi.org/10.1039/c9nj00964gopenalex-snapshot
Organoselenium small molecules as catalysts for the oxidative functionalization of organic molecules
inferred← citeshttps://doi.org/10.1039/c9nj02505gopenalex-snapshot
New methodology of nucleophilic substitution at three different centers of a seleniranium intermediate in reactions of 2-bromomethyl-1,3-thiaselenole with mercapto benzazoles
inferred← citeshttps://doi.org/10.1039/c9qo00620fopenalex-snapshot
Recent progress in selenium-catalyzed organic reactions
inferred← citeshttps://doi.org/10.1039/d0cc01079kopenalex-snapshot
An organoselenium-catalyzed N 1 - and N 2 -selective aza-Wacker reaction of alkenes with benzotriazoles
inferred← citeshttps://doi.org/10.1039/d0qo01175dopenalex-snapshot
Metal-free synthesis of 3-chalcogenyl chromones from alkynyl aryl ketones and diorganyl diselenides/disulfides mediated by PIFA
inferred← citeshttps://doi.org/10.1039/d1gc02783bopenalex-snapshot
Bifunctionalization of unsaturated bonds via carboxylative cyclization with CO 2 : a sustainable access to heterocyclic compounds
inferred← citeshttps://doi.org/10.1039/d1qo00851jopenalex-snapshot
Copper-catalyzed domino synthesis of benzo[ d ]imidazo[5,1- b ][1,3]selenazoles involving sequential intermolecular cycloaddition and intramolecular Ullmann-type C–Se bond formation
inferred← citeshttps://doi.org/10.1039/d2cc01901aopenalex-snapshot
Electrochemical selenium–π–acid promoted hydration of alkynyl phosphonates
inferred← citeshttps://doi.org/10.1039/d2cc02181aopenalex-snapshot
A base-free copper-assisted synthesis of C 2 -symmetric spirotelluranes and biaryls based on divergent stoichiometry of Na 2 Te
inferred← citeshttps://doi.org/10.1039/d2nj05976bopenalex-snapshot
Thiol modifier effects of diphenyl diselenides: insight from experiment and DFT calculations
inferred← citeshttps://doi.org/10.1039/d2ob00254jopenalex-snapshot
Synthesis of 1,3-diselenyl-dihydroisobenzofurans via electrochemical radical selenylation with substituted o -divinylbenzenes and diselenides
inferred← citeshttps://doi.org/10.1039/d2ra05387jopenalex-snapshot
PIFA-mediated selenylative spirocyclization of indolyl ynones: facile access to selenated spiro[cyclopentenone-1,3′-indoles]
inferred← citeshttps://doi.org/10.1039/d2sc00954dopenalex-snapshot
Regiocontrolled allylic functionalization of internal alkene via selenium-π-acid catalysis guided by boron substitution
inferred← citeshttps://doi.org/10.1039/d3nj03720gopenalex-snapshot
Synthesis of tetrasubstituted selenophenes by DBU-induced sequential three-component coupling and intramolecular cyclization
inferred← citeshttps://doi.org/10.1039/d3ob00150dopenalex-snapshot
Regioselective C–H chalcogenylation and halogenation of arenes and alkenes under metal-free conditions
inferred← citeshttps://doi.org/10.1039/d3qo01457fopenalex-snapshot
Organo-catalyzed C2,3–H aminochalcogenation of indoles with secondary (aliphatic) amines
inferred← citeshttps://doi.org/10.1039/d4gc01006jopenalex-snapshot
Mechanochemical aerobic oxidative Heck coupling by polymer-assisted grinding: cyclodextrin additive facilitating regioselectivity control
inferred← citeshttps://doi.org/10.1039/d6nj01095dopenalex-snapshot
Efficient one-pot synthesis of 2-(sulfanylselanylmethyl)-1,3-thiaselenoles using 2-bromomethyl-1,3-thiaselenole
inferred← citeshttps://doi.org/10.1055/s-0037-1610683openalex-snapshot
Regio- and Stereoselective Synthesis of a Novel Family of Unsaturated Compounds with the S–Se Bond and Their Cyclization to 2,3-Dihydro-1,4-thiaselenines
inferred← citeshttps://doi.org/10.1055/sos-sd-225-00023openalex-snapshot
2.2 Catalytic Oxidations with Hypervalent Iodine
inferred← citeshttps://doi.org/10.1080/00397911.2018.1479760openalex-snapshot
Ultrasound-assisted rapid synthesis of β-cyanoepoxides using hypervalent iodine reagents
inferred← citeshttps://doi.org/10.1080/17568919.2024.2435254openalex-snapshot
Organoselenium compounds beyond antioxidants
inferred← citeshttps://doi.org/10.1246/cl.200015openalex-snapshot
Organoseleniums: Generated and Exploited in Oxidative Reactions
inferred← citeshttps://doi.org/10.1515/psr-2017-0131openalex-snapshot
Selenium and Tellurium Electrophiles in Organic Synthesis
inferred← citeshttps://doi.org/10.2139/ssrn.4968864openalex-snapshot
How Did Hypervalent Iodide Oxidant Species Influence Reaction Yield of Organoselenium-Catalzyed Oxidative Ring-Closing Reaction of (E)-4-Phenylbut-3-Enoic Acid? A Theoretical Study
inferred← citeshttps://doi.org/10.2174/0929867329666220801165849openalex-snapshot
Synthesis and Antioxidant Properties of Organoselenium Compounds
inferred← citeshttps://doi.org/10.2174/1385272822666180803123137openalex-snapshot
Organodiselenides: Organic Catalysis and Drug Design Learning from Glutathione Peroxidase
inferred← citeshttps://doi.org/10.2174/1385272827666230103110651openalex-snapshot
Iodine(III)-Based Hypervalent Iodine Electrophiles in Organic Synthesis
inferred← citeshttps://doi.org/10.2174/1570179418666210920150142openalex-snapshot
A Review on the Role of Transition Metals in Selenylation Reactions
inferred← citeshttps://doi.org/10.2174/1570179419666220211102602openalex-snapshot
Recent Advances in Organoselenium Catalysis
inferred← citeshttps://doi.org/10.24820/ark.5550190.p011.418openalex-snapshot
Hypervalent iodine-mediated synthesis and late-stage functionalization of heterocycles
inferred← citeshttps://doi.org/10.24820/ark.5550190.p011.483openalex-snapshot
Hypervalent iodine chemistry and light: photochemical reactions involving hypervalent iodine chemistry
inferred← citeshttps://doi.org/10.3184/174751912x13445852334047openalex-snapshot
Iodobenzene Diacetate (PIDA)/Zn(II)-Mediated Oxidation and Cleavage of C–C Bond: Formation of Substituted N-aryl Carbamoyl Methyl Diacetates and Derivatives from 3-oxo-butanamides
inferred← citeshttps://doi.org/10.33774/chemrxiv-2021-0lw7kopenalex-snapshot
Regiocontrolled Allylic Functionalization of Internal Alkene via Selenium-pi-Acid Catalysis Guided by Boron Substitution
inferred← citeshttps://doi.org/10.3389/fchem.2020.00705openalex-snapshot
Hypervalent Iodine Reagents in Palladium-Catalyzed Oxidative Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.3390/molecules200610095openalex-snapshot
Synthesis and Biological Evaluation of 2-Picolylamide-Based Diselenides with Non-Bonded Interactions
inferred← citeshttps://doi.org/10.3390/molecules22050835openalex-snapshot
Electrophilic Selenium Catalysis with Electrophilic N-F Reagents as the Oxidants
inferred← citeshttps://doi.org/10.3390/molecules27123900openalex-snapshot
Palladium-Catalyzed Organic Reactions Involving Hypervalent Iodine Reagents
inferred← citeshttps://doi.org/10.3390/molecules28135250openalex-snapshot
Iodine(V)-Based Oxidants in Oxidation Reactions
inferred← citeshttps://doi.org/10.3390/nano10061237openalex-snapshot
Exploration of the Interaction Strength at the Interface of Anionic Chalcogen Anchors and Gold (111)-Based Nanomaterials
inferred← citeshttps://doi.org/10.3762/bjoc.14.152openalex-snapshot
Synthesis of spirocyclic scaffolds using hypervalent iodine reagents
inferred← citeshttps://doi.org/10.3762/bjoc.16.47openalex-snapshot
Regio- and stereoselective synthesis of new ensembles of diversely functionalized 1,3-thiaselenol-2-ylmethyl selenides by a double rearrangement reaction
inferred← citeshttps://doi.org/10.3762/bjoc.20.243openalex-snapshot
Recent advances in transition-metal-free arylation reactions involving hypervalent iodine salts
inferred← citeshttps://doi.org/10.3762/bjoc.8.38openalex-snapshot
Organic synthesis using (diacetoxyiodo)benzene (DIB): Unexpected and novel oxidation of 3-oxo-butanamides to 2,2-dihalo-N-phenylacetamides
inferred← citeshttps://doi.org/10.59761/rcr5143openalex-snapshot
Metal complexes with selenium-based ligands in organic synthesis
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