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Catalytic Use of Selenium Electrophiles in Cyclizations
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-3757(20010803)113:15<2893::aid-ange2893>3.0.co;2-fopenalex-snapshot
IBX - neue Reaktionen mit einem alten Reagens
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Preparation of a New Chiral Non-Racemic Sulfur-Containing Diselenide and Applications in Asymmetric Synthesis
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Tetrafluor‐IBA und ‐IBX: hypervalente Iodreagentien
inferredcites →https://doi.org/10.1002/anie.200702313openalex-snapshot
Tetrafluoro‐IBA and‐IBX: Hypervalent Iodine Reagents
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Index: Angew. Chem. Int. Ed. 2007
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The Efficient Direct Synthesis of N,O‐Acetal Compounds as Key Intermediates of Discorhabdin A: Oxidative Fragmentation Reaction of α‐Amino Acids or β‐Amino Alcohols by Using Hypervalent Iodine( III ) Reagents
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Stereoselective access to functionalized β-γ unsaturated acids
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New nitrogen containing chiral diselenides: synthesis and asymmetric addition reactions to olefins
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Catalytic asymmetric oxyselenenylation–elimination reactions using chiral selenium compounds
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Asymmetric oxyselenenylation–deselenenylation reactions of alkenes induced by camphor diselenide and ammonium persulfate. A convenient one-pot synthesis of enantiomerically enriched allylic alcohols and ethers
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Novel azido-phenylselenenylation of double bonds. Evidence for a free-radical process
inferredcites →https://doi.org/10.1021/jo00024a021openalex-snapshot
Addition of semidione radicals to arenediazonium ions: synthesis of 1,1-diacyl-2-arylhydrazines
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Synthetic approaches to butenolides
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The Synthesis of gama-Alkylidenebutenolides
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New Developments with Chiral Electrophilic Selenium Reagents
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Stereoselective Reactions of Organoselenium Reagents Including Catalysis
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Phenyliodine(III) bis(trifluoroacetate) 1
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Phenyliodine( III ) Bis(trifluoroacetate)
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Phenyliodine( III ) Bis(trifluoroacetate)
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Organoselenium Chemistry
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Organoselenium‐Catalyzed Regioselective C−H Pyridination of 1,3‐Dienes and Alkenes
inferred← citeshttps://doi.org/10.1002/anie.201711599openalex-snapshot
Photocatalytic Aerobic Phosphatation of Alkenes
inferred← citeshttps://doi.org/10.1002/anie.201914421openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202016220openalex-snapshot
Enantioselective Synthesis of α‐Aryl‐β2‐Amino‐Esters by Cooperative Isothiourea and Brønsted Acid Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202100801openalex-snapshot
Redox‐Neutral Selenium‐Catalysed Isomerisation of para ‐Hydroxamic Acids into para ‐Aminophenols
inferred← citeshttps://doi.org/10.1002/anie.202202621openalex-snapshot
Cooperative Palladium/Isothiourea Catalyzed Enantioselective Formal (3+2) Cycloaddition of Vinylcyclopropanes and α,β‐Unsaturated Esters
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Photocatalytic Aerobic Cyclization of N ‐Propargylamides Enabled by Selenium‐π‐Acid Catalysis
inferred← citeshttps://doi.org/10.1002/chem.202302386openalex-snapshot
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Catalytic Use of Selenium Electrophiles in Cyclizations.
inferred← citeshttps://doi.org/10.1002/ejoc.200801171openalex-snapshot
Recent Advances in Organoselenium Chemistry
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Diselenide‐ and Disulfide‐Mediated Synthesis of Isocoumarins
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Elemental Iodine or Diphenyl Diselenide in the [Bis(trifluoroacetoxy)iodo]benzene‐Mediated Conversion of Alkynes into 1,2‐Diketones
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Organoselenium Compounds as Reagents and Catalysts to Develop New Green Protocols
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4.07 Electrophilic Cyclization
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Facile oxidative hydrolysis of acetals to esters using hypervalent iodine(III)/LiBr combination in water
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.08.049openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.2c02688openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.7b01245openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.2c00117openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03811openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03026openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03543openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.5c01692openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03737openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acscatal.3c04443openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acscatal.7b01216openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acscatal.7b03829openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c0cc02352copenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c1cy00184aopenalex-snapshot
IBX in aqueous medium: a green protocol for the Biginelli reaction
inferred← citeshttps://doi.org/10.1039/c1dt11022eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c1gc16243hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c3ra23188gopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c5cc10245fopenalex-snapshot
Organoselenium and DMAP co-catalysis: regioselective synthesis of medium-sized halolactones and bromooxepanes from unactivated alkenes
inferred← citeshttps://doi.org/10.1039/c5ob02125aopenalex-snapshot
Hg/Pt-catalyzed conversion of bromo alkynamines/alkynols to saturated and unsaturated γ-butyrolactams/lactones via intramolecular electrophilic cyclization
inferred← citeshttps://doi.org/10.1039/c5qo00179jopenalex-snapshot
Organoselenium-catalyzed synthesis of indoles through intramolecular C–H amination
inferred← citeshttps://doi.org/10.1039/c6qo00820hopenalex-snapshot
Efficient synthesis of multiply substituted butenolides from keto acids and terminal alkynes promoted by combined acids
inferred← citeshttps://doi.org/10.1039/c9cc00101hopenalex-snapshot
Ruthenium catalyzes the synthesis of γ-butenolides fused with cyclohexanones
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/c9qo01497gopenalex-snapshot
Chelation-assisted transition metal-catalysed C–H chalcogenylations
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/d1sc03860eopenalex-snapshot
Catalytic enantioselective synthesis of 1,4-dihydropyridines via the addition of C(1)-ammonium enolates to pyridinium salts
inferred← citeshttps://doi.org/10.1039/d2cc01901aopenalex-snapshot
Electrochemical selenium–π–acid promoted hydration of alkynyl phosphonates
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/d3nj01423aopenalex-snapshot
A redox active organodiselenide as an efficacious catalyst for the synthesis of oxygen-containing heterocyclic compounds
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/d5cc06222eopenalex-snapshot
Unlocking reactivity potential of gem -dihaloolefins: access to Halo-functionalized 1,4-naphthoquinones via intramolecular radical oxidative cyclization
inferred← citeshttps://doi.org/10.1039/d5sc08502kopenalex-snapshot
Se-catalyzed enantioselective lactamization enabled by a N -fluorosulfonyl group: total synthesis of diaporisoindole A
inferred← citeshttps://doi.org/10.1055/a-2550-1785openalex-snapshot
Tetrahydrofuran Ring Construction through Tandem Iodocyclizations: Synthesis of Hagen’s Gland Lactones, a Pheromone of Idea leuconoe, an Oxylipid, and Related Compounds
inferred← citeshttps://doi.org/10.1055/s-0041-1737291openalex-snapshot
Divergent Synthesis of Chalcogenylated Quinolin-2-ones and Spiro[4,5]trienones via Intramolecular Cyclization of N-Arylpropynamides Mediated by Diselenides/Disulfides and PhICl2
inferred← citeshttps://doi.org/10.1080/00397911.2019.1652914openalex-snapshot
A facile synthesis of γ-butenolides via cyclization of 3-alkenoic acids with dimethyl sulfoxide and oxalyl bromide
inferred← citeshttps://doi.org/10.1080/10426500801901053openalex-snapshot
Catalytic Addition-Elimination Reactions Towards Butenolides
inferred← citeshttps://doi.org/10.1080/10426501003772169openalex-snapshot
Synthesis of Indoles, 3,1-Benzoxazines, and Quinolines from 2-Alkenylanilides and Active Seleniums
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/10.2174/1570179419666220211102602openalex-snapshot
Recent Advances in Organoselenium Catalysis
inferred← citeshttps://doi.org/10.2174/1570193x17666200220130735openalex-snapshot
Δα,β-Butenolides [Furan-2(5H)-ones]: Ring Construction Approaches and Biological Aspects - A Mini-Review
inferred← citeshttps://doi.org/10.3184/174751912x13402955389383openalex-snapshot
Efficient Synthesis of the Odourant, 2-Nonen-4-Olide
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/10.3390/molecules22050835openalex-snapshot
Electrophilic Selenium Catalysis with Electrophilic N-F Reagents as the Oxidants
inferred← citeshttps://doi.org/10.3390/polym13101632openalex-snapshot
Synthesis of Selenium-Containing Polystyrene Microspheres and Using as Catalyst for Oxidation of Acrolein
inferred← citeshttps://doi.org/10.3998/ark.5550190.p009.113openalex-snapshot
A convenient alkoxylselenenylation of alkenes promoted by p-toluenesulfonic acid
inferred← citeshttps://doi.org/10.59761/rcr5143openalex-snapshot
Metal complexes with selenium-based ligands in organic synthesis
inferred← citeshttps://doi.org/10.6023/cjoc202109036openalex-snapshot
Organoselenium-Catalyzed Conversion of Oximes to Nitriles or Ketones
inferred← citeshttps://doi.org/10.6023/cjoc202508009openalex-snapshot
Research Progress in Electrophilic Selenium-Catalyzed Rearrangement Reactions
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