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Isoselenazolones as Catalysts for the Activation of Bromine: Bromolactonization of Alkenoic Acids and Oxidation of Alcohols

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

inferredcites →https://doi.org/10.1002/(sici)1521-3765(19990503)5:5<1411::aid-chem1411>3.0.co;2-mopenalex-snapshot

Intramolecular Se⋅⋅⋅N Nonbonding Interactions in Low-Valent Organoselenium Derivatives: A Detailed Study by1H and77Se NMR Spectroscopy and X-Ray Crystallography

inferredcites →https://doi.org/10.1002/1521-3765(20020301)8:5<1125::aid-chem1125>3.0.co;2-iopenalex-snapshot

New and Efficient Chiral Selenium Electrophiles

inferredcites →https://doi.org/10.1002/anie.200461889openalex-snapshot

Clean and Highly Selective Oxidation of Alcohols in an Ionic Liquid by Using an Ion‐Supported Hypervalent Iodine( III ) Reagent

inferredcites →https://doi.org/10.1002/anie.200500573openalex-snapshot

Asymmetric Carboselenenylation Reaction of Alkenes with Aromatic Compounds

inferredcites →https://doi.org/10.1002/anie.200601817openalex-snapshot

Hypervalent Iodine Goes Catalytic

inferredcites →https://doi.org/10.1002/anie.200604943openalex-snapshot

Lewis Base Catalysis in Organic Synthesis

inferredcites →https://doi.org/10.1002/anie.200702313openalex-snapshot

Tetrafluoro‐IBA and‐IBX: Hypervalent Iodine Reagents

inferredcites →https://doi.org/10.1002/anie.200806148openalex-snapshot

Fast Synthesis of Benzofluorenes by Selenium‐Mediated Carbocyclizations

inferredcites →https://doi.org/10.1002/anie.200903834openalex-snapshot

Et 2 SBr⋅SbCl 5 Br: An Effective Reagent for Direct Bromonium‐Induced Polyene Cyclizations

inferredcites →https://doi.org/10.1002/anie.201202079openalex-snapshot

Enantioselective Bromolactonization Using an S‐Alkyl Thiocarbamate Catalyst

inferredcites →https://doi.org/10.1002/chem.19970031123openalex-snapshot

Asymmetric Addition Reactions with Optimized Selenium Electrophiles

inferredcites →https://doi.org/10.1002/chem.200800462openalex-snapshot

Electrophilic Bromination of Alkenes: Environmental, Health and Safety Aspects of New Alternative Methods

inferredcites →https://doi.org/10.1002/chem.201100930openalex-snapshot

Synthesis, Structure, and Glutathione Peroxidase‐Like Activity of Amino Acid Containing Ebselen Analogues and Diaryl Diselenides

inferredcites →https://doi.org/10.1002/chin.200545049openalex-snapshot

In situ Generation of o‐Iodoxybenzoic Acid (IBX) and the Catalytic Use of It in Oxidation Reactions in the Presence of Oxone as a Co‐oxidant.

inferredcites →https://doi.org/10.1002/ejic.200300603openalex-snapshot

Synthesis, Structural Characterization and Fluorescence Properties of Organoselenium Compounds Bearing a Ligand Containing Both Bulky and Nonbonding Groups − The First Observation of Both Intramolecular Se···N and Se···O Interactions in a Diselenide Structure

inferredcites →https://doi.org/10.1002/ejic.200900669openalex-snapshot

Stable Selenenium Cations: Unusual Reactivity and Excellent Glutathione Peroxidase‐Like Activity

inferredcites →https://doi.org/10.1002/ejoc.200400326openalex-snapshot

Convenient Synthesis, Characterization and GPx‐Like Catalytic Activity of Novel Ebselen Derivatives

inferredcites →https://doi.org/10.1002/ejoc.201000308openalex-snapshot

Diselenide‐ and Disulfide‐Mediated Synthesis of Isocoumarins

inferredcites →https://doi.org/10.1002/ejoc.201101373openalex-snapshot

Asymmetric Methoxyselenenylations with Chiral Selenium Electrophiles

inferredcites →https://doi.org/10.1016/0040-4039(95)02121-3openalex-snapshot

Copper (II) bromide on alumina: A new reagent for bromolactonization

inferredcites →https://doi.org/10.1016/j.tet.2004.04.014openalex-snapshot

Halo- and selenolactonisation: the two major strategies for cyclofunctionalisation

inferredcites →https://doi.org/10.1016/j.tet.2005.12.072openalex-snapshot

Selenium-catalyzed oxidative halogenation

inferredcites →https://doi.org/10.1016/j.tet.2010.03.037openalex-snapshot

A two-step mimic for direct, asymmetric bromonium- and chloronium-induced polyene cyclizations

inferredcites →https://doi.org/10.1016/j.tet.2011.09.141openalex-snapshot

Copper catalyzed/mediated synthetic methodology for ebselen and related isoselenazolones

inferredcites →https://doi.org/10.1016/j.tetlet.2006.12.042openalex-snapshot

Dimethylformamide, dimethylacetamide and tetramethylguanidine as nucleophilic organocatalysts for the transfer of electrophilic bromine from N-bromosuccinimide to alkenes

inferredcites →https://doi.org/10.1016/j.tetlet.2007.06.112openalex-snapshot

Amidines as potent nucleophilic organocatalysts for the transfer of electrophilic bromine from N-bromosuccinimide to alkenes

inferredcites →https://doi.org/10.1016/j.tetlet.2007.08.113openalex-snapshot

An efficient process for the bromolactamization of unsaturated acids

inferredcites →https://doi.org/10.1016/j.tetlet.2010.04.113openalex-snapshot

Molecular sieves as an efficient and recyclable catalyst for bromolactonization and bromoacetoxylation reactions

inferredcites →https://doi.org/10.1016/j.tetlet.2011.07.049openalex-snapshot

Studies toward Lewis basic thiocarbamate and thiourea mediated bromolactonization: the effect of a trace amount of water on the reactivity and enantioselectivity

inferredcites →https://doi.org/10.1016/j.tetlet.2011.10.067openalex-snapshot

Strained dimethyl 2-(bromoselanyl)-5-tert-butylisophthalate: a reactive precursor for the synthesis of ebselen analogs

inferredcites →https://doi.org/10.1016/s0040-4020(98)00946-6openalex-snapshot

Chiral selenium compounds in organic synthesis

inferredcites →https://doi.org/10.1016/s0040-4020(98)01133-8openalex-snapshot

Asymmetric electrophilic methoxyselenenylations and cyclizations with 3-camphorseleno derivatives

inferredcites →https://doi.org/10.1016/s0040-4039(00)76844-4openalex-snapshot

Synthesis of chiral diferrocenyl diselenides and their application to asymmetric reactions

inferredcites →https://doi.org/10.1021/ja002649+openalex-snapshot

Dendrimeric Organochalcogen Catalysts for the Activation of Hydrogen Peroxide: Improved Catalytic Activity through Statistical Effects and Cooperativity in Successive Generations

inferredcites →https://doi.org/10.1021/ja00316a044openalex-snapshot

1,3-Asymmetric induction: highly stereoselective synthesis of 2,4-trans-disubstituted γ-butyrolactones and γ-butyrothiolactones

inferredcites →https://doi.org/10.1021/ja00345a055openalex-snapshot

The total synthesis of ionophore antibiotics. A convergent synthesis of lasalocid A (X537A)

inferredcites →https://doi.org/10.1021/ja0367593openalex-snapshot

Dendrimeric Organochalcogen Catalysts for the Activation of Hydrogen Peroxide: Origins of the “Dendrimer Effect” with Catalysts Terminating in Phenylseleno Groups

inferredcites →https://doi.org/10.1021/ja1048972openalex-snapshot

Asymmetric Bromolactonization Using Amino-thiocarbamate Catalyst

inferredcites →https://doi.org/10.1021/ja201627hopenalex-snapshot

Enantioselective Bromoaminocyclization Using Amino–Thiocarbamate Catalysts

inferredcites →https://doi.org/10.1021/ja806304sopenalex-snapshot

Biomimetic Asymmetric Total Synthesis of (−)-Laurefucin via an Organoselenium-Mediated Intramolecular Hydroxyetherification

inferredcites →https://doi.org/10.1021/ja807110nopenalex-snapshot

2-Iodoxybenzenesulfonic Acid as an Extremely Active Catalyst for the Selective Oxidation of Alcohols to Aldehydes, Ketones, Carboxylic Acids, and Enones with Oxone

inferredcites →https://doi.org/10.1021/ja953187gopenalex-snapshot

Positive Halogens from Halides and Hydrogen Peroxide with Organotellurium Catalysts

inferredcites →https://doi.org/10.1021/ja974177dopenalex-snapshot

Mechanistic Course of the Asymmetric Methoxyselenenylation Reaction

inferredcites →https://doi.org/10.1021/ja990473+openalex-snapshot

Origin of Stereoselectivities in Asymmetric Alkoxyselenenylations

inferredcites →https://doi.org/10.1021/jo00001a089openalex-snapshot

Synthesis of castasterone and formal synthesis of brassinolide from stigmasterol via a selenosulfonation approach

inferredcites →https://doi.org/10.1021/jo00008a039openalex-snapshot

Formation and electrophilic reactions of benzeneselenenyl p-toluenesulfonate. Preparation and properties of addition products with acetylenes

inferredcites →https://doi.org/10.1021/jo00010a045openalex-snapshot

Organoselenium- and proton-mediated cyclization reactions of allylic amides and thioamides. Syntheses of 2-oxazolines and 2-thiazolines

inferredcites →https://doi.org/10.1021/jo00061a009openalex-snapshot

Functional group manipulation via organoselenium- and halogen-induced cyclofunctionalization/hydrolysis of allylic benzimidates, tertiary benzamides, and benzamidines. Regioflexible synthesis of amino alcohol derivatives

inferredcites →https://doi.org/10.1021/jo00108a038openalex-snapshot

1,3-Diselenetanes and 1,3-Dithietanes Derived from Camphor. Formation, Structure, Stereochemistry, and Oxidation to Selenoxide and Sulfoxide Products

inferredcites →https://doi.org/10.1021/jo00118a031openalex-snapshot

Synthesis of [R,S;R,S]- and [S,R;S,R]-Bis[2-[1-(dimethylamino)ethyl]ferrocenyl] Diselenides and Their Application to Asymmetric Selenoxide Elimination and [2,3]Sigmatropic Rearrangement

inferredcites →https://doi.org/10.1021/jo00149a011openalex-snapshot

Oxidation of alcohols with dimethyl selenide-N-chlorosuccinimide complex

inferredcites →https://doi.org/10.1021/jo00174a018openalex-snapshot

Reaction of olefins with a mixture of phenylselenenyl chloride and mercury(II) thiocyanate. Selective syntheses of .beta.-(phenylseleno)alkyl isothiocyanates as precursors of vinylic isothiocyanates

inferredcites →https://doi.org/10.1021/jo00194a024openalex-snapshot

Pyridylseleno group in organic synthesis. Preparation and oxidation of .alpha.-(2-pyridylseleno) carbonyl compounds leading to .alpha.,.beta.-unsaturated ketones and aldehydes

inferredcites →https://doi.org/10.1021/jo00227a026openalex-snapshot

Phenylselenium trichloride in organic synthesis. Reaction with unsaturated compounds. Preparation of vinylic chlorides via selenoxide elimination

inferredcites →https://doi.org/10.1021/jo00252a028openalex-snapshot

Methods for the introduction of a phenylselenium dichloride group into the .alpha.-position of carbonyl compounds. Syntheses of enones

inferredcites →https://doi.org/10.1021/jo00265a031openalex-snapshot

Acetoxyselenylation of olefins for the preparation of vinylic and allylic acetates

inferredcites →https://doi.org/10.1021/jo00360a017openalex-snapshot

Intramolecular amidoselenation of N-alkenyl amides: formation of nitrogen heterocycles

inferredcites →https://doi.org/10.1021/jo00386a022openalex-snapshot

Organoselenium-induced cyclization of olefinic imidates and amides. Selective synthesis of lactams or iminolactones

inferredcites →https://doi.org/10.1021/jo016061copenalex-snapshot

Asymmetric Methoxyselenenylations and Cyclizations with 3-Camphorseleno Electrophiles Containing Oxime Substituents at C-2. Formation of an Unusual Oxaselenazole from an Oxime-Substituted Selenenyl Bromide

inferredcites →https://doi.org/10.1021/jo026751wopenalex-snapshot

Mild Oxidation of Alcohols with o-Iodoxybenzoic Acid (IBX) in Water/Acetone Mixture in the Presence of β-Cyclodextrin

inferredcites →https://doi.org/10.1021/jo048460oopenalex-snapshot

Selenium-Catalyzed Halolactonization: Nucleophilic Activation of Electrophilic Halogenating Reagents

inferredcites →https://doi.org/10.1021/jo0610457openalex-snapshot

On the Mechanism of the Selenolactonization Reaction with Selenenyl Halides

inferredcites →https://doi.org/10.1021/jo0612067openalex-snapshot

Oxidations of Secondary Alcohols to Ketones Using Easily Recyclable Bis(trifluoroacetate) Adducts of Fluorous Alkyl Iodides, CF3(CF2)n-1I(OCOCF3)2

inferredcites →https://doi.org/10.1021/jo202221copenalex-snapshot

An Enantioselective Approach toward 3,4-Dihydroisocoumarin through the Bromocyclization of Styrene-type Carboxylic Acids

inferredcites →https://doi.org/10.1021/jo202269popenalex-snapshot

Lewis Base Catalysis by Thiourea: N-Bromosuccinimide-Mediated Oxidation of Alcohols

inferredcites →https://doi.org/10.1021/jo300313vopenalex-snapshot

Cyclic Seleninate Esters as Catalysts for the Oxidation of Sulfides to Sulfoxides, Epoxidation of Alkenes, and Conversion of Enamines to α-Hydroxyketones

inferredcites →https://doi.org/10.1021/jo801234eopenalex-snapshot

A Xerogel-Sequestered Selenoxide Catalyst for Brominations with Hydrogen Peroxide and Sodium Bromide in an Aqueous Environment

inferredcites →https://doi.org/10.1021/jo801730jopenalex-snapshot

Facile Photochemical Transformation of Alkyl Aryl Selenides to the Corresponding Carbonyl Compounds by Molecular Oxygen: Use of Selenides as Masked Carbonyl Groups

inferredcites →https://doi.org/10.1021/jo901628aopenalex-snapshot

One-Pot Facile Synthesis of Substituted Isoindolinones via an Ugi Four-Component Condensation/Diels−Alder Cycloaddition/ Deselenization−Aromatization Sequence

inferredcites →https://doi.org/10.1021/jo952093mopenalex-snapshot

Chiral Diselenides in the Total Synthesis of (+)-Samin

inferredcites →https://doi.org/10.1021/jo981224ropenalex-snapshot

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inferredcites →https://doi.org/10.1021/jo990730topenalex-snapshot

Cycloaddition Reactions of 1-Phenylseleno-2-(p-toluenesulfonyl)ethyne

inferredcites →https://doi.org/10.1021/jo9917644openalex-snapshot

Novel Preparation of α,β-Unsaturated Aldehydes. Benzeneselenolate Promotes Elimination of HBr from α-Bromoacetals

inferredcites →https://doi.org/10.1021/ol000187zopenalex-snapshot

New Chiral Auxiliaries for Highly Stereoselective Asymmetric Methoxyselenenylations

inferredcites →https://doi.org/10.1021/ol005829xopenalex-snapshot

Pyrrolidines from β-Aminoselenides via Radical Cyclization. Diastereoselectivity Control by the N-Substituent

inferredcites →https://doi.org/10.1021/ol016127qopenalex-snapshot

Construction of Tetrahydrofuran-3-ones from Readily Available Organochalcogen Precursors via Radical Carbonylation/Reductive Cyclization

inferredcites →https://doi.org/10.1021/ol016429sopenalex-snapshot

Diastereocontrol by Trialkylaluminums in the Synthesis of Tetrahydrofurans via Radical Cyclization

inferredcites →https://doi.org/10.1021/ol0164435openalex-snapshot

Novel Polymer-Bound Chiral Selenium Electrophiles

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A Very Mild and Chemoselective Oxidation of Alcohols to Carbonyl Compounds

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TEMPO-Catalyzed Aerobic Oxidation of Alcohols to Aldehydes and Ketones in Ionic Liquid [bmim][PF 6 ]

inferredcites →https://doi.org/10.1021/ol026038topenalex-snapshot

Diastereocontrol by a Hydroxyl Auxiliary in the Synthesis of Pyrrolidines via Radical Cyclization

inferredcites →https://doi.org/10.1021/ol036525oopenalex-snapshot

Selective Selenocatalytic Allylic Chlorination

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In Situ Generation of o -Iodoxybenzoic Acid (IBX) and the Catalytic Use of It in Oxidation Reactions in the Presence of Oxone as a Co-oxidant

inferredcites →https://doi.org/10.1021/ol071223yopenalex-snapshot

Catalytic Use of Selenium Electrophiles in Cyclizations

inferredcites →https://doi.org/10.1021/ol100274eopenalex-snapshot

Selenium-Mediated Synthesis of Biaryls through Rearrangement

inferredcites →https://doi.org/10.1021/ol100615jopenalex-snapshot

Asymmetric, Organocatalytic, Three-Step Synthesis of α-Hydroxy-(E)-β,γ-unsaturated Esters

inferredcites →https://doi.org/10.1021/ol101879kopenalex-snapshot

Site-Selective Modification of Vitamin D Analogue (Deltanoid) through a Resin-Based Version of Organoselenium 2,3-Sigmatropic Rearrangement

inferredcites →https://doi.org/10.1021/ol102027jopenalex-snapshot

Cu-Catalyzed Efficient Synthetic Methodology for Ebselen and Related Se−N Heterocycles

inferredcites →https://doi.org/10.1021/ol200840eopenalex-snapshot

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inferredcites →https://doi.org/10.1021/ol202800kopenalex-snapshot

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inferredcites →https://doi.org/10.1021/ol990836aopenalex-snapshot

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Chelate Ring Size Effect on the Reactivity of [2-(2-Phenyl-5,6-dihydro-4H-1,3-oxazinyl)]lithium and Se···N Interactions in Low-Valent Organoselenium Compounds: Facile Isolation of Diorganotriselenide

inferredcites →https://doi.org/10.1021/om049908eopenalex-snapshot

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inferredcites →https://doi.org/10.1021/om900134popenalex-snapshot

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inferredcites →https://doi.org/10.1021/om960476kopenalex-snapshot

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inferredcites →https://doi.org/10.1039/a803494jopenalex-snapshot

Catalytic asymmetric imidation of selenides into selenimides

inferredcites →https://doi.org/10.1039/a806707dopenalex-snapshot

Asymmetric methoxyselenenylations with camphor-based selenium electrophiles

inferredcites →https://doi.org/10.1039/b312364bopenalex-snapshot

Synthesis of organochalcogens stabilized by intramolecular non-bonded interactions of sterically unhindered 2-phenyl-2-oxazolineElectronic supplementary information (ESI) available: 77Se NMR spectrum of 14, molecular structure of 16 and packing diagram of 15. See…

inferredcites →https://doi.org/10.1039/b410576aopenalex-snapshot

Selenocatalytic α-halogenation

inferredcites →https://doi.org/10.1039/b600455eopenalex-snapshot

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inferredcites →https://doi.org/10.1039/b604130bopenalex-snapshot

Ortho-substituted iodobenzenes as novel organocatalysts for bromination of alkenes

inferredcites →https://doi.org/10.1039/b816914dopenalex-snapshot

The generation and trapping of enantiopure bromonium ions

inferredcites →https://doi.org/10.1039/c1cc12152aopenalex-snapshot

Photoluminescent selenospirocyclic and selenotetracyclic derivatives by domino reactions of amines and imines

inferredcites →https://doi.org/10.1039/c1cc13619dopenalex-snapshot

Enantiospecific bromonium ion generation and intramolecular capture: a model system for asymmetric bromonium ion-induced polyene cyclisations

inferredcites →https://doi.org/10.1039/c39770000484openalex-snapshot

New route to bicyclic lactones: use of benzeneselenenyl chloride

inferredcites →https://doi.org/10.1039/c39950002321openalex-snapshot

Highly selective asymmetric intramolecular selenocyclisation

inferredcites →https://doi.org/10.1039/cc9960002567openalex-snapshot

Asymmetric cyclization of unsaturated alcohols and carboxylic acids with camphor-based selenium electrophiles

inferredcites →https://doi.org/10.1039/dt9960002719openalex-snapshot

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inferredcites →https://doi.org/10.1055/s-1984-30956openalex-snapshot

A Convenient Oxidation of Halomethylarenes and Alcohols to Aldehydes with Dimethyl Selenoxide and Potassium Benzeneselenite

inferredcites →https://doi.org/10.1055/s-1988-27790openalex-snapshot

A Convenient Method for Bromolactonization

inferredcites →https://doi.org/10.1055/s-1995-5216openalex-snapshot

Diels-Alder Reactions of 1-(Phenylseleno)-2-(p-toluenesulfonyl)ethyne - A Novel Dienophile And Ketene Equivalent

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(Diacetoxyiodo)benzene-Lithium Bromide as a Convenient Electrophilic Br+Source

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Lewis base catalysis of bromo- and iodolactonization, and cycloetherification

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PREPARATION AND X-RAY CRYSTAL STRUCTURES OF TWO ALIPHATIC SELENENYL BROMIDES STABILIZED BY N─SE COORDINATION

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Retrospect of Se and Te Chemistry

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SYNTHESIS OF Et2SBr0SbCl5Br AND ITS USE IN BIOMIMETIC BROMINATIVE POLYENE CYCLIZATIONS

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inferred← citeshttps://doi.org/10.1002/chem.202302386openalex-snapshot

Mechanistic Study on Selenium‐ and Sulfur‐Mediated Isomerization of Hydroxamic Acids

inferred← citeshttps://doi.org/10.1002/chem.202401650openalex-snapshot

Telluronium‐Catalyzed Halogenation Reactions: Chalcogen‐Bond Activation of N ‐Halosuccinimides and Catalysis

inferred← citeshttps://doi.org/10.1002/chin.201309021openalex-snapshot

ChemInform Abstract: Isoselenazolones as Catalysts for the Activation of Bromine: Bromolactonization of Alkenoic Acids and Oxidation of Alcohols.

inferred← citeshttps://doi.org/10.1002/hc.21164openalex-snapshot

Synthesis and Antioxidant Activities of Novel Chiral Ebselen Analogues

inferred← citeshttps://doi.org/10.1002/slct.202002474openalex-snapshot

Synthesis of Various Derivatives of [1,3]Selenazolo[4,5‐d]pyrimidine and Exploitation of These Heterocyclic Systems as Antibacterial, Antifungal, and Anticancer Agents

inferred← citeshttps://doi.org/10.1002/slct.202004029openalex-snapshot

Insights into the Recent Synthetic Advances of Organoselenium Compounds

inferred← citeshttps://doi.org/10.1007/978-3-319-92405-2_1openalex-snapshot

Organoselenium Compounds as Reagents and Catalysts to Develop New Green Protocols

inferred← citeshttps://doi.org/10.1007/978-981-15-1490-6_8openalex-snapshot

Functional Enzyme Mimics for Oxidative Halogenation Reactions that Combat Biofilm Formation

inferred← citeshttps://doi.org/10.1007/s00894-015-2901-0openalex-snapshot

On the properties of Se ⋯N interaction: the analysis of substituent effects by energy decomposition and orbital interaction

inferred← citeshttps://doi.org/10.1007/s11164-021-04478-8openalex-snapshot

Nano-Co3O4-catalyzed microwave-assisted one-pot synthesis of some seleno [2 , 3-b ] pyridine/quinoline derivatives

inferred← citeshttps://doi.org/10.1007/s40010-014-0129-5openalex-snapshot

Crystal Structure Studies on Some of Benzamide Ring Substituted Isoselenazolones and Symmetric Diaryl Monoselenides Derived from Benzamides

inferred← citeshttps://doi.org/10.1007/s40010-016-0306-9openalex-snapshot

Cinchona-Alkaloids Based Isoselenazolones: Synthesis and Their Catalytic Reactivity in Asymmetric Bromolactonization of Alkenoic Acid

inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00113-xopenalex-snapshot

1,2-Selenazoles

inferred← citeshttps://doi.org/10.1016/b978-0-12-819449-2.00009-4openalex-snapshot

Oxygen-transfer reactions catalyzed by organoselenium compounds

inferred← citeshttps://doi.org/10.1016/bs.aihch.2025.01.004openalex-snapshot

Recent advances in the synthesis and reactions of selenium heterocycles

inferred← citeshttps://doi.org/10.1016/j.ccr.2016.01.003openalex-snapshot

Recent advances in the chemistry of selenium-containing heterocycles: Five-membered ring systems

inferred← citeshttps://doi.org/10.1016/j.ccr.2016.09.016openalex-snapshot

Recent advances in the chemistry of selenium-containing heterocycles: Six-membered ring systems

inferred← citeshttps://doi.org/10.1016/j.ccr.2020.213586openalex-snapshot

Zero-, one-, two- and three-dimensional supramolecular architectures sustained by Se…O chalcogen bonding: A crystallographic survey

inferred← citeshttps://doi.org/10.1016/j.comptc.2014.07.014openalex-snapshot

Computational study on the mechanism of uncatalyzed and selenium-based catalyzed bromolactonization

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.04.199openalex-snapshot

The first selenium containing chitin and chitosan derivatives: Combined synthetic, catalytic and biological studies

inferred← citeshttps://doi.org/10.1016/j.mcat.2026.116359openalex-snapshot

Photoelectrocatalytic bromolactonization with NaBr as the bromine source coupled with hydrogen evolution

inferred← citeshttps://doi.org/10.1016/j.tet.2013.04.113openalex-snapshot

Potassium tert-butoxide-mediated synthesis of unsymmetrical diaryl ethers, sulfides and selenides from aryl bromides

inferred← citeshttps://doi.org/10.1016/j.tet.2013.10.049openalex-snapshot

Chiral benzisoselenazolones: conformational analysis based on experimental and DFT calculated 77Se NMR

inferred← citeshttps://doi.org/10.1016/j.tet.2014.01.030openalex-snapshot

A convenient and efficient copper-catalyzed synthesis of unsymmetrical and symmetrical diaryl chalcogenides from arylboronic acids in ethanol at room temperature

inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.01.009openalex-snapshot

Synthesis of chiral butenolides using amino-thiocarbamate-catalyzed asymmetric bromolactonization

inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153567openalex-snapshot

Electrochemical oxidative bromolactonization of unsaturated carboxylic acids with sodium bromide: Synthesis of bromomethylated γ-lactones

inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.156074openalex-snapshot

Novel and scalable synthesis process development for the antibiotic lefamulin

inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00400openalex-snapshot

Use of Bromine and Bromo-Organic Compounds in Organic Synthesis

inferred← citeshttps://doi.org/10.1021/acs.inorgchem.2c00651openalex-snapshot

Tetravalent Spiroselenurane Catalysts: Intramolecular Se···N Chalcogen Bond-Driven Catalytic Disproportionation of H2O2 to H2O and O2 and Activation of I2 and NBS

inferred← citeshttps://doi.org/10.1021/acs.joc.2c02831openalex-snapshot

Introduction of Methyl Group in Substituted Isoselenazolones: Catalytic and Mechanistic Study

inferred← citeshttps://doi.org/10.1021/acs.joc.5b01497openalex-snapshot

Divergent Synthesis of α,γ-Disubstituted γ-Butyrolactones through Diastereoselective Bromolactonization with Alkali Metal Bromide: Asymmetric Total Synthesis of (+)-Dubiusamine C

inferred← citeshttps://doi.org/10.1021/acs.joc.5c02477openalex-snapshot

Visible-Light-Mediated C(sp 3 )–Se Coupling: Synthesis of GPx-Mimic Unsymmetrical Aryl–Secondary Alkyl Selenoether Antioxidants

inferred← citeshttps://doi.org/10.1021/acs.joc.9b00029openalex-snapshot

Lipophilic Indole-Catalyzed Intermolecular Bromoesterification of Olefins in Nonpolar Media

inferred← citeshttps://doi.org/10.1021/acs.joc.9b01294openalex-snapshot

Organoselenium Accelerated Bromolactonization Reaction

inferred← citeshttps://doi.org/10.1021/acs.oprd.3c00189openalex-snapshot

Stereoinvertive Deoxyamination of trans-2-Aminocyclohexanol Using Bose–Mitsunobu Azidation and Staudinger Reaction for the Stereoselective Synthesis of Edoxaban

inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01928openalex-snapshot

Zwitterion-Catalyzed Intermolecular Bromoesterifications

inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03546openalex-snapshot

Nitroxyl Catalysts for Six-Membered Ring Bromolactonization and Intermolecular Bromoesterification of Alkenes with Carboxylic Acids

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00213openalex-snapshot

Organoselenium-Catalyzed, Hydroxy-Controlled Regio- and Stereoselective Amination of Terminal Alkenes: Efficient Synthesis of 3-Amino Allylic Alcohols

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02557openalex-snapshot

Lewis Basic Sulfide Catalyzed Electrophilic Bromocyclization of Cyclopropylmethyl Amide

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00116openalex-snapshot

Synthesis of Benzoisoselenazolone Derivatives by Nickel-Catalyzed Dehydrogenative Direct Selenation of C(sp 2 )–H Bonds with Elemental Selenium in Air

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01392openalex-snapshot

Chiral Selenide-Catalyzed Enantioselective Construction of Saturated Trifluoromethylthiolated Azaheterocycles

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02406openalex-snapshot

Combination of Lewis Basic Selenium Catalysis and Redox Selenium Chemistry: Synthesis of Trifluoromethylthiolated Tertiary Alcohols with Alkenes

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02834openalex-snapshot

Access to Saturated Thiocyano-Containing Azaheterocycles via Selenide-Catalyzed Regio- and Stereoselective Thiocyanoaminocyclization of Alkenes

inferred← citeshttps://doi.org/10.1021/acscatal.2c05414openalex-snapshot

Study and Applications of Tetrasubstituted Hypervalent Selenium–Halogen Species in Catalytic Electrophilic Halogenations

inferred← citeshttps://doi.org/10.1021/ja311202eopenalex-snapshot

C2-Symmetric Cyclic Selenium-Catalyzed Enantioselective Bromoaminocyclization

inferred← citeshttps://doi.org/10.1021/ja5029155openalex-snapshot

Catalytic Asymmetric Bromoetherification and Desymmetrization of Olefinic 1,3-Diols with C2-Symmetric Sulfides

inferred← citeshttps://doi.org/10.1021/jp312383fopenalex-snapshot

The Nature of the Interaction of Dimethylselenide with IIIA Group Element Compounds

inferred← citeshttps://doi.org/10.1021/ol400249xopenalex-snapshot

Lewis Basic Selenium Catalyzed Chloroamidation of Olefins Using Nitriles as the Nucleophiles

inferred← citeshttps://doi.org/10.1039/bk9781839167386-00334openalex-snapshot

The Chemistry of Selenium-catalyzed Redox Processes

inferred← citeshttps://doi.org/10.1039/c3oc90011hopenalex-snapshot

Synthetic methods: part (ii) oxidation and reduction methods

inferred← citeshttps://doi.org/10.1039/c4ob00027gopenalex-snapshot

An ebselen like catalyst with enhanced GPx activity via a selenol intermediate

inferred← citeshttps://doi.org/10.1039/c4ra00381kopenalex-snapshot

Sensitive and regenerable organochalcogen probes for the colorimetric detection of thiols

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/c5dt04356eopenalex-snapshot

Synthesis and structural characterization of monomeric mercury( ii ) selenolate complexes derived from 2-phenylbenzamide ligands

inferred← citeshttps://doi.org/10.1039/c5ra19851hopenalex-snapshot

Oxidative oxygen-nucleophilic bromo-cyclization of alkenyl carbonyl compounds without organic wastes using alkali metal reagents in green solvent

inferred← citeshttps://doi.org/10.1039/c6nj00658bopenalex-snapshot

Organoselenium-catalyzed vicinal dichlorination of unsaturated phosphonates

inferred← citeshttps://doi.org/10.1039/c6ob00756bopenalex-snapshot

Trifluoroacetic acid catalyzed highly regioselective bromocyclization of styrene-type carboxylic acid

inferred← citeshttps://doi.org/10.1039/c8cy02274gopenalex-snapshot

Selenium reagents as catalysts

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/c9ob00449aopenalex-snapshot

Nickel( ii )-catalyzed C(sp 2 )–H sulfuration/annulation with elemental sulfur: selective access to benzoisothiazolones

inferred← citeshttps://doi.org/10.1039/c9qo00620fopenalex-snapshot

Recent progress in selenium-catalyzed organic reactions

inferred← citeshttps://doi.org/10.1039/c9sc05335bopenalex-snapshot

Selenophosphoramide-catalyzed diamination and oxyamination of alkenes

inferred← citeshttps://doi.org/10.1039/d0nj01605eopenalex-snapshot

Fast and easy conversion of ortho amidoaryldiselenides into the corresponding ebselen-like derivatives driven by theoretical investigations

inferred← citeshttps://doi.org/10.1039/d3cc01920aopenalex-snapshot

NBS-induced intramolecular annulation reactions for the divergent synthesis of fused- and spirocyclic indolines

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/d4ob01553copenalex-snapshot

Recent progress in the organoselenium-catalyzed difunctionalization of alkenes

inferred← citeshttps://doi.org/10.1055/a-2706-0614openalex-snapshot

Photoinduced and N-Bromosuccinimide-Initiated Esterification of Aromatic acids and Terminal Alkynes with Alcohols

inferred← citeshttps://doi.org/10.1055/s-0037-1609560openalex-snapshot

A Highly Efficient Method for the Bromination of Alkenes, Alkynes and Ketones Using Dimethyl Sulfoxide and Oxalyl Bromide

inferred← citeshttps://doi.org/10.1080/00397911.2022.2028843openalex-snapshot

Electrochemical bromolactonization of alkenoic acids with carbon tetrabromide: Synthesis of bromomethylated γ-lactones

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/10.1515/psr-2018-0061openalex-snapshot

Organoselenium and organotellurium compounds containing chalcogen-oxygen bonds in organic synthesis or related processes

inferred← citeshttps://doi.org/10.2174/1570179419666220211102602openalex-snapshot

Recent Advances in Organoselenium Catalysis

inferred← citeshttps://doi.org/10.3390/ijms22052769openalex-snapshot

A Review of the Pharmacological Activities and Recent Synthetic Advances of γ-Butyrolactones

inferred← citeshttps://doi.org/10.3390/molecules200610205openalex-snapshot

Developments in Synthetic Application of Selenium(IV) Oxide and Organoselenium Compounds as Oxygen Donors and Oxygen-Transfer Agents

inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.76.11openalex-snapshot

Direct Thiolation and Selenation of Aryl C-H Bonds Catalyzed by Palladium or Nickel

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