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Catalytic, stereospecific syn-dichlorination of alkenes
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Tetraethylammonium Trichloride: A Versatile Reagent for Chlorinations and Oxidations
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Bystanding F + Oxidants Enable Selective Reductive Elimination from High‐Valent Metal Centers in Catalysis
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Direct Oxidative Allylic and Vinylic Amination of Alkenes through Selenium Catalysis
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ChemInform Abstract: Selective Manganese‐Mediated Transformations Using the Combination KMnO4/Me3SiCl.
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Recent Advances in the Total Synthesis of Chlorosulfolipids
inferredcites →https://doi.org/10.1002/poc.2946openalex-snapshot
Acidities of strong neutral Brønsted acids in different media
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Recent progress toward synthesis of chlorosulfolipids: total synthesis and methodology
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Fluorination of olefins with PhSeF3, PhSeF5 and PhTeF5
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-generated molybdenum (VI) reagent for -chlorination of alkenes
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1,2-functionalization of cyclohexane using selenium intermediates
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The cis chlorination of alkenes using selenium reagents
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Reactions of selenoxides: Thermal -elimination and H218O exchange.
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Selective manganese-mediated transformations using the combination:
inferredcites →https://doi.org/10.1021/ar400246wopenalex-snapshot
Approaches to the Chemical Synthesis of the Chlorosulfolipids
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Chlorination of alkenes and alkynes with molybdenum(V) chloride
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Chlorination Studies of Unsaturated Materials in Nonpolar Media. IV. The Ionic Pathway for Alkylated Ethylenes. Products and Relative Reactivities1
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Acetolysis Rates of the cis- and trans-2-Chloro- and 2-Bromocyclohexyl p-Bromobenzenesulfonates
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Chlorinations with Sulfuryl Chloride. II. The Peroxide-Catalyzed Reaction of Sulfuryl Chloride with Ethylenic Compounds
inferredcites →https://doi.org/10.1021/ja202555mopenalex-snapshot
Enantioselective Dichlorination of Allylic Alcohols
inferredcites →https://doi.org/10.1021/ja906461hopenalex-snapshot
Conformational and Configurational Analysis in the Study and Synthesis of Chlorinated Natural Products
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/jo005521jopenalex-snapshot
Self-Consistent Spectrophotometric Basicity Scale in Acetonitrile Covering the Range between Pyridine and DBU
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Mechanism of the addition of chlorine to olefins with iodobenzene dichloride
inferredcites →https://doi.org/10.1021/jo01337a046openalex-snapshot
Selenium-catalyzed nonradical chlorination of olefins with N-chlorosuccinimide
inferredcites →https://doi.org/10.1021/jo020053uopenalex-snapshot
Novel Process for Generating Useful Electrophiles from Common Anions Using Selectfluor® Fluorination Agent
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General Approach to the Synthesis of the Chlorosulfolipids Danicalipin A, Mytilipin A, and Malhamensilipin A in Enantioenriched Form
inferredcites →https://doi.org/10.1021/jo802093dopenalex-snapshot
Enantiocontrolled Synthesis of Polychlorinated Hydrocarbon Motifs: A Nucleophilic Multiple Chlorination Process Revisited
inferredcites →https://doi.org/10.1021/ol036525oopenalex-snapshot
Selective Selenocatalytic Allylic Chlorination
inferredcites →https://doi.org/10.1021/ol102010hopenalex-snapshot
Catalysis of Phosphorus(V)-Mediated Transformations: Dichlorination Reactions of Epoxides Under Appel Conditions
inferredcites →https://doi.org/10.1038/nature07734openalex-snapshot
Total synthesis of a chlorosulpholipid cytotoxin associated with seafood poisoning
inferredcites →https://doi.org/10.1039/c3ob27345hopenalex-snapshot
Dichlorination of olefins with NCS/Ph3P
inferredcites →https://doi.org/10.1039/c3ob40670aopenalex-snapshot
Convenient in situ generation of various dichlorinating agents from oxone and chloride: diastereoselective dichlorination of allylic and homoallylic alcohol derivatives
inferredcites →https://doi.org/10.1055/s-1977-24526openalex-snapshot
Synthetic Methods and Reactions; 391. Phase Transfer Catalyst Promoted Halogenation of Alkenes with Hydrohalic Acid/Hydrogen Peroxide
inferredcites →https://doi.org/10.1080/10426500108046638openalex-snapshot
Inter and Intramolecular Nucleophilic Substitutions of Activated Phenylselanyl Groups
inferredcites →https://doi.org/10.1126/science.157.3792.997openalex-snapshot
Chlorination of Unsaturated Compounds in Nonpolar Media
inferredcites →https://doi.org/10.1139/v74-538openalex-snapshot
The Addition of Arylselenium Trichlorides vs. Areneselenenyl Chlorides to cis- and trans-1-Phenylpropene
inferredcites →https://doi.org/10.1201/9781420007282openalex-snapshot
Comprehensive Handbook of Chemical Bond Energies
inferredcites →https://doi.org/10.1246/bcsj.47.3121openalex-snapshot
Molybdenum(V) Chloride as a Reagent for cis Chlorination of Olefins
inferredcites →https://doi.org/10.1246/bcsj.47.692openalex-snapshot
The Chlorination of Olefins with Antimony(V) Chloride
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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A Theoretical Study on Organoselenium-Catalyzed Exo-Selective Oxidative Ring-Closing Reaction Promoted by 3 Different N-F Oxidants: Active Catalytic Species Screening, Reaction Mechanism, Origin of Exo-/Endo- and (E)-/(Z)- Selectivities, and the Influence of Different Reagents on Reaction Yields
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Enantioselective Halofunctionalization of Alkenes
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Selenenate Anions (PhSeO−) as Organocatalyst: Synthesis of trans‐Stilbenes and a PPV Derivative
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Stereoselektive Halogenierungen in der Naturstoffsynthese
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Katalytische stereoselektive Dihalogenierung von Alkenen: Herausforderungen und Chancen
inferred← citeshttps://doi.org/10.1002/ange.201511672openalex-snapshot
Bioisosteric Exchange of C‐Chloro and Methyl Substituents: Synthesis and Initial Biological Studies of Atpenin A5 Analogues
inferred← citeshttps://doi.org/10.1002/ange.201610657openalex-snapshot
Organoselenium‐Catalyzed Regioselective C−H Pyridination of 1,3‐Dienes and Alkenes
inferred← citeshttps://doi.org/10.1002/ange.201810328openalex-snapshot
Enantioselective, Catalytic Vicinal Difluorination of Alkenes
inferred← citeshttps://doi.org/10.1002/ange.201901777openalex-snapshot
Organokatalytische, enantioselektive Dichlorierung unfunktionalisierter Alkene
inferred← citeshttps://doi.org/10.1002/ange.202010801openalex-snapshot
Visible‐Light‐Induced Vicinal Dichlorination of Alkenes through LMCT Excitation of CuCl2
inferred← citeshttps://doi.org/10.1002/ange.202206265openalex-snapshot
Green‐Light‐Driven Reductive Elimination of Chlorine from a Carbene‐Xanthylium Gold(III) Complex
inferred← citeshttps://doi.org/10.1002/ange.202208611openalex-snapshot
Wasserstoffbrücken‐modulierte Nukleofugalität von SeIII‐Spezies ermöglicht photoredox‐katalytische Semipinakol‐Prozesse
inferred← citeshttps://doi.org/10.1002/anie.201506388openalex-snapshot
Stereoselective Halogenation in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1002/anie.201507152openalex-snapshot
Catalytic, Stereoselective Dihalogenation of Alkenes: Challenges and Opportunities
inferred← citeshttps://doi.org/10.1002/anie.201511672openalex-snapshot
Bioisosteric Exchange of C‐Chloro and Methyl Substituents: Synthesis and Initial Biological Studies of Atpenin A5 Analogues
inferred← citeshttps://doi.org/10.1002/anie.201610657openalex-snapshot
Organoselenium‐Catalyzed Regioselective C−H Pyridination of 1,3‐Dienes and Alkenes
inferred← citeshttps://doi.org/10.1002/anie.201810328openalex-snapshot
Enantioselective, Catalytic Vicinal Difluorination of Alkenes
inferred← citeshttps://doi.org/10.1002/anie.201901777openalex-snapshot
Organocatalytic, Enantioselective Dichlorination of Unfunctionalized Alkenes
inferred← citeshttps://doi.org/10.1002/anie.202010801openalex-snapshot
Visible‐Light‐Induced Vicinal Dichlorination of Alkenes through LMCT Excitation of CuCl 2
inferred← citeshttps://doi.org/10.1002/anie.202206265openalex-snapshot
Green‐Light‐Driven Reductive Elimination of Chlorine from a Carbene‐Xanthylium Gold(III) Complex
inferred← citeshttps://doi.org/10.1002/anie.202208611openalex-snapshot
Hydrogen‐Bond‐Modulated Nucleofugality of SeIII Species to Enable Photoredox‐Catalytic Semipinacol Manifolds
inferred← citeshttps://doi.org/10.1002/aoc.4332openalex-snapshot
Design and Preparation of Poly‐Selenides: Easily Fabricated and Efficient Organoselenium Materials for Heavy Metal Removing and Recycling
inferred← citeshttps://doi.org/10.1002/aoc.4599openalex-snapshot
A cost‐effective shortcut to prepare organoselenium catalysts via decarboxylative coupling of phenylacetic acid with elemental selenium
inferred← citeshttps://doi.org/10.1002/asia.202400053openalex-snapshot
Decennary Update on Oxidative‐Rearrangement Involving 1,2‐Aryl C−C Migration Around Alkenes: Synthetic and Mechanistic Insights
inferred← citeshttps://doi.org/10.1002/cctc.201501309openalex-snapshot
Organoselenium‐Catalyzed Oxidative Ring Expansion of Methylenecyclopropanes with Hydrogen Peroxide
inferred← citeshttps://doi.org/10.1002/cctc.201801548openalex-snapshot
NIS/TBHP Induced Regioselective Selenation of (Hetero)Arenes via Direct C−H Functionalization
inferred← citeshttps://doi.org/10.1002/cctc.202300803openalex-snapshot
Enantioselective Ni‐Catalyzed Three‐Component Dicarbofunctionalization of Alkenes
inferred← citeshttps://doi.org/10.1002/chem.201600800openalex-snapshot
Regioselective, Solvent‐ and Metal‐Free Chalcogenation of Imidazo[1,2‐ a ]pyridines by Employing I 2 /DMSO as the Catalytic Oxidation System
inferred← citeshttps://doi.org/10.1002/chem.201804504openalex-snapshot
Multiple Halogenation of Aliphatic C−H Bonds within the Hofmann–Löffler Manifold
inferred← citeshttps://doi.org/10.1002/chem.202003176openalex-snapshot
Enantioselective Dihalogenation of Alkenes
inferred← citeshttps://doi.org/10.1002/chem.202103316openalex-snapshot
The Electrochemical cis‐Chlorination of Alkenes
inferred← citeshttps://doi.org/10.1002/chem.202304074openalex-snapshot
Asymmetric Synthesis with Organoselenium Compounds – The Past Twelve Years
inferred← citeshttps://doi.org/10.1002/chem.202402261openalex-snapshot
Halogen and Chalcogen Activation by Nucleophilic Catalysis
inferred← citeshttps://doi.org/10.1002/chin.201519058openalex-snapshot
ChemInform Abstract: Catalytic, Stereospecific syn‐Dichlorination of Alkenes.
inferred← citeshttps://doi.org/10.1002/cptc.202000239openalex-snapshot
Preparation of Oxazole Acetals from N‐Propargylamides Enabled by Visible‐Light‐Promoted Selenium‐π‐Acid Catalysis
inferred← citeshttps://doi.org/10.1002/ejoc.202100811openalex-snapshot
Dihalogenation of Alkenes Using Combinations of N‐Halosuccinimides and Alkali Metal Halides
inferred← citeshttps://doi.org/10.1002/ejoc.202100912openalex-snapshot
Continuous Flow Organocatalytic Chlorination of Alkenes
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Copper‐Catalyzed Three‐Component Reaction of Oxadiazoles, Elemental Se/S and Aryl Iodides: Synthesis of Chalcogenyl (Se/S)‐Oxadiazoles
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K 2 S 2 O 8 ‐Mediated Efficient Oxidative Deoximation of Flavonoid Oximes under Mild Reaction Conditions
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Dichlorination of Alkenes Using 1,3‐Dichloro‐5,5‐Dimethylhydantoin and ZnCl 2
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Selectfluor‐Mediated N‐Methylation, N‐Methylenesulfonylmethylation and Methylenethiomethylation of Isatins in Dimethyl Sulfoxide
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Organoselenium Compounds as Reagents and Catalysts to Develop New Green Protocols
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Synthesis and Derivatization of Alkenes and Alkynes
inferred← citeshttps://doi.org/10.1007/s00894-018-3624-9openalex-snapshot
Reaction mechanism of organoselenium-catalyzed syn-dichlorination of alkenes: a DFT study
inferred← citeshttps://doi.org/10.1007/s11144-025-02949-2openalex-snapshot
A theoretical study of organoselenium-catalyzed oxidative ring-closing reaction: structure/selectivity/yield relationships
inferred← citeshttps://doi.org/10.1007/s11426-017-9158-yopenalex-snapshot
Visible light-promoted, iodine-catalyzed selenoalkoxylation of olefins with diselenides and alcohols in the presence of hydrogen peroxide/air oxidant: an efficient access to α-alkoxyl selenides
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14760-2openalex-snapshot
Three-Membered Rings With One Selenium or Tellurium Atom
inferred← citeshttps://doi.org/10.1016/b978-0-32-390644-9.00106-2openalex-snapshot
Diastereoselective Halogenation Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-32-390644-9.00132-3openalex-snapshot
Olefin Difunctionalization With the Same Atoms; 1,2-Difunctionalization of Olefins With the Same Heteroatom (Excluding O and N)
inferred← citeshttps://doi.org/10.1016/b978-0-323-95893-6.00001-3openalex-snapshot
Visible light–driven organic synthesis under Rose Bengal photocatalysis
inferred← citeshttps://doi.org/10.1016/j.apcata.2017.05.007openalex-snapshot
A scalable production of anisonitrile through organoselenium-catalyzed dehydration of anisaldoxime under solventless conditions
inferred← citeshttps://doi.org/10.1016/j.apsusc.2018.07.193openalex-snapshot
The influence of sulfate on selenate sorption on Mg-Al-CO3 layered double hydroxides prepared by fine inorganic sol-gel synthesis studied by X-ray photoelectron spectroscopy
inferred← citeshttps://doi.org/10.1016/j.cclet.2026.112695openalex-snapshot
Recent advances in the chiral organoselenium catalyzed enantioselective functionalization of alkenes and arenes
inferred← citeshttps://doi.org/10.1016/j.cej.2015.05.070openalex-snapshot
Static and dynamic adsorptive removal of selenite and selenate by alkoxide-free sol–gel-generated Mg–Al–CO3 layered double hydroxide: Effect of competing ions
inferred← citeshttps://doi.org/10.1016/j.gresc.2022.10.008openalex-snapshot
Electrooxidative trifunctionalization of alkenes with N-chlorosuccinimide and ArSSAr/ArSH to α,β-dichloride arylsulfoxides
inferred← citeshttps://doi.org/10.1016/j.mcat.2024.114442openalex-snapshot
Both N-F oxidant and NaF determined reaction yield in the organoselenium-catalyzed oxidative ring-closing reaction of unsaturated alcohol: A theoretical study
inferred← citeshttps://doi.org/10.1016/j.tet.2019.04.042openalex-snapshot
One-pot preparation of (RSe)2CF2 and (RS)2CF2 compounds via insertion of TMSCF3-derived difluorocarbene into diselenides and disulfides
inferred← citeshttps://doi.org/10.1016/j.tet.2019.05.054openalex-snapshot
Organoselenium-catalyzed enantioselective syn-dichlorination of unbiased alkenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.09.088openalex-snapshot
Proline and secondary amine co-catalyzed condensation of cyclobutanone with aldehydes: a facile access to 2-methylenecyclobutanones under near neutral conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.151756openalex-snapshot
Enantioselective bromolactonization of aryl functionalized alkenoic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152180openalex-snapshot
One-pot modular synthesis of β-chalcogen amides via regioselective 2-oxazolines ring-opening reaction promoted by indium chalcogenolates under microwave irradiation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153028openalex-snapshot
Difluorinative-hydroxylation and C-3 functionalization (halogenation/SCN/NO) of imidazopyridine using Selectfluor as fluorine source or oxidant respectively
inferred← citeshttps://doi.org/10.1021/acs.chemrev.4c00661openalex-snapshot
Nitrogen-Based Organofluorine Functional Molecules: Synthesis and Applications
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00012openalex-snapshot
Electrochemically Enabled Selenium Catalytic Synthesis of 2,1-Benzoxazoles from o -Nitrophenylacetylenes
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02271openalex-snapshot
Lewis Base Catalyzed, Sulfenium Ion Initiated Enantioselective, Spiroketalization Cascade
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01200openalex-snapshot
POCl3/Sulfoxide and AcCl/Sulfoxide Mediated Chlorination of Pyrrolo[2,1-a]isoquinolines
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00151openalex-snapshot
HCl/DMSO/HFIP-Mediated Chlorination of Pyrrolo[2,1-a]isoquinolines and Other Electron-Rich Heteroarenes
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00295openalex-snapshot
Difunctionalization of Alkenes Using 1-Chloro-1,2-benziodoxol-3-(1H)-one
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00634openalex-snapshot
Ru(II)-Catalyzed Direct C(sp 2 )–H Activation/Selenylation of Arenes with Selenyl Chlorides
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00780openalex-snapshot
Internally Directed Stereochemical Alteration of Alkene Dihalogenation
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01245openalex-snapshot
Organoselenium-Catalyzed Oxidative C═C Bond Cleavage: A Relatively Green Oxidation of Alkenes into Carbonyl Compounds with Hydrogen Peroxide
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01281openalex-snapshot
Photocatalytic E → Z Isomerization of Polarized Alkenes Inspired by the Visual Cycle: Mechanistic Dichotomy and Origin of Selectivity
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01671openalex-snapshot
Deconstructing the Catalytic, Vicinal Difluorination of Alkenes: HF-Free Synthesis and Structural Study of p-TolIF2
inferred← citeshttps://doi.org/10.1021/acs.joc.7b03197openalex-snapshot
Synthesis of Vicinal Dichlorides via Activation of Aliphatic Terminal Epoxides with Triphosgene and Pyridine
inferred← citeshttps://doi.org/10.1021/acs.organomet.5c00413openalex-snapshot
Catalytic Wacker Oxidation of Tetrasubstituted Alkenes: Efficient Access to gem -Dimethyl Ketones
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01258openalex-snapshot
Phosphorus(III)-Mediated, Tandem Deoxygenative Geminal Chlorofluorination of 1,2-Diketones
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01288openalex-snapshot
Organoseleno-Catalyzed Synthesis of α,β-Unsaturated α′-Alkoxy Ketones from Allenes Enabled by Se···O Interactions
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c00117openalex-snapshot
Organoselenium-Catalyzed Cross-Dehydrogenative Coupling of Alkenes and Azlactones
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02377openalex-snapshot
Organoselenium-Catalyzed Enantioselective Synthesis of 2-Oxazolidinones from Alkenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04084openalex-snapshot
Halodealkenylation: Ozonolysis and Catalytic Fe II with Vitamin C Convert C(sp 3 )–C(sp 2 ) Bonds to C(sp 3 )–Halide Bonds
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01156openalex-snapshot
Selenium-Catalyzed Oxidative C(sp2)–H Amination of Alkenes Exemplified in the Expedient Synthesis of (Aza-)Indoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03011openalex-snapshot
Dehydration of Aldoximes Using PhSe(O)OH as the Pre-Catalyst in Air
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03543openalex-snapshot
Organoselenium-Catalyzed Synthesis of Oxygen- and Nitrogen-Containing Heterocycles
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03649openalex-snapshot
Regioselective Synthesis of Carbonyl-Containing Alkyl Chlorides via Silver-Catalyzed Ring-Opening Chlorination of Cycloalkanols
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03692openalex-snapshot
Enantioselective Addition of Alkynes to α,α-Dichlorinated Aldehydes
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00241openalex-snapshot
Enriching Alkene syn -Dihalogenation: Aryl Alkene, Bromine, Regio-Reversion, and Stereoconvergency
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.7b02613openalex-snapshot
Selenium–Iodine Cooperative Catalyst for Chlorocyclization of Tryptamine Derivatives
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02751openalex-snapshot
Iron-Promoted Difunctionalization of Alkenes by Phenylselenylation/1,2-Aryl Migration
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03121openalex-snapshot
Furfuryl Cation Induced Cascade Formal [3 + 2] Cycloaddition/Double Ring-Opening/Chlorination: An Approach to Chlorine-Containing Complex Triazoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02624openalex-snapshot
Neighboring Effect of Intramolecular Chlorine Atoms on Epoxide Opening Reaction by Chloride Anions
inferred← citeshttps://doi.org/10.1021/acsami.2c17966openalex-snapshot
Reactive Chlorine Capture by Dichlorination of Alkene Linkers in Metal–Organic Frameworks
inferred← citeshttps://doi.org/10.1021/acsami.5c25977openalex-snapshot
Synchronous Reconfiguring Triplet Energy and Excitonic Redox Charge-Transfer States in Dual-Chromogen-Embedded Conjugated Polymers for Diverse and Efficient Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/acscatal.4c01327openalex-snapshot
Intermolecular Aza-Wacker Coupling of Alkenes with Azoles by Photo-Aerobic Selenium-π-Acid Multicatalysis
inferred← citeshttps://doi.org/10.1021/acscatal.4c03660openalex-snapshot
Merging Iron-Mediated Radical Ligand Transfer (RLT) Catalysis and Mechanochemistry for Facile Dihalogenation of Alkenes
inferred← citeshttps://doi.org/10.1021/acscatal.5c06722openalex-snapshot
Metal-Free Radical Vicinal Dihalogenation of Olefins Enabled by Synergetic Photocatalytic Energy Transfer and Halogen-Atom Transfer
inferred← citeshttps://doi.org/10.1021/acscatal.6b02155openalex-snapshot
Catalytic, Vicinal Difluorination of Olefins: Creating a Hybrid, Chiral Bioisostere of the Trifluoromethyl and Ethyl Groups
inferred← citeshttps://doi.org/10.1021/acscatal.7b01216openalex-snapshot
Oxidative Alkene Functionalizations via Selenium-π-Acid Catalysis
inferred← citeshttps://doi.org/10.1021/acscatal.7b02729openalex-snapshot
Mechanistic and Synthetic Investigations on the Dual Selenium-π-Acid/Photoredox Catalysis in the Context of the Aerobic Dehydrogenative Lactonization of Alkenoic Acids
inferred← citeshttps://doi.org/10.1021/acscatal.7b03829openalex-snapshot
Organoselenium-Catalyzed Oxidative Allylic Fluorination with Electrophilic N–F Reagent
inferred← citeshttps://doi.org/10.1021/acscatal.8b01069openalex-snapshot
An Electrocatalytic Approach to the Radical Difunctionalization of Alkenes
inferred← citeshttps://doi.org/10.1021/acscatal.8b01236openalex-snapshot
Mechanistic Studies on the Anodic Functionalization of Alkenes Catalyzed by Diselenides
inferred← citeshttps://doi.org/10.1021/acscatal.8b01565openalex-snapshot
Thiourea–I2 as Lewis Base–Lewis Acid Cooperative Catalysts for Iodochlorination of Alkene with In Situ-Generated I–Cl
inferred← citeshttps://doi.org/10.1021/acscatal.8b01595openalex-snapshot
Selenium-π-Acid Catalyzed Oxidative Functionalization of Alkynes: Facile Access to Ynones and Multisubstituted Oxazoles
inferred← citeshttps://doi.org/10.1021/acscatal.9b02313openalex-snapshot
Catalytic Vicinal Dichlorination of Unactivated Alkenes
inferred← citeshttps://doi.org/10.1021/acsomega.7b00445openalex-snapshot
Metal- and Solvent-Free Approach to Access 3-Se/S-Chromones from the Cyclization of Enaminones in the Presence of Dichalcogenides Catalyzed by KIO3
inferred← citeshttps://doi.org/10.1021/jacs.1c06750openalex-snapshot
Catalytic, Enantioselective Syn -Oxyamination of Alkenes
inferred← citeshttps://doi.org/10.1021/jacs.1c07511openalex-snapshot
Asymmetric Total Synthesis of Clionastatins A and B
inferred← citeshttps://doi.org/10.1021/jacs.4c09039openalex-snapshot
Visible-Light-Mediated Vicinal Dihalogenation of Unsaturated C–C Bonds Using Dual-Functional Group Transfer Reagents
inferred← citeshttps://doi.org/10.1021/jacs.4c16413openalex-snapshot
An Atomically Dispersed Mn Photocatalyst for Vicinal Dichlorination of Nonactivated Alkenes
inferred← citeshttps://doi.org/10.1021/jacs.5b01384openalex-snapshot
Catalytic Chemo-, Regio-, and Enantioselective Bromochlorination of Allylic Alcohols
inferred← citeshttps://doi.org/10.1021/jacs.5c16205openalex-snapshot
Modulation of the Electronic and Vibrational Landscape in Lead Organic Chalcogenides
inferred← citeshttps://doi.org/10.1021/jacs.5c20677openalex-snapshot
Catalytic Remote Dihalogenation of Alkenes Induced by Transposition of Esters
inferred← citeshttps://doi.org/10.1021/jacs.6b01183openalex-snapshot
Catalytic Difluorination of Olefins
inferred← citeshttps://doi.org/10.1021/jacs.6b01643openalex-snapshot
Catalytic Enantioselective Dihalogenation and the Selective Synthesis of (−)-Deschloromytilipin A and (−)-Danicalipin A
inferred← citeshttps://doi.org/10.1021/jacs.6b09203openalex-snapshot
Highly Regio- and Enantioselective Vicinal Dihalogenation of Allyl Amides
inferred← citeshttps://doi.org/10.1021/jacs.7b02076openalex-snapshot
Enantioselective Synthesis of anti–syn-Trihalides and anti–syn–anti-Tetrahalides via Asymmetric β-Elimination
inferred← citeshttps://doi.org/10.1021/jacs.7b09388openalex-snapshot
Electrocatalytic Radical Dichlorination of Alkenes with Nucleophilic Chlorine Sources
inferred← citeshttps://doi.org/10.1021/jacs.9b01891openalex-snapshot
Triazine Functionalized Porous Covalent Organic Framework for Photo-organocatalytic E–Z Isomerization of Olefins
inferred← citeshttps://doi.org/10.1021/jacs.9b11261openalex-snapshot
Catalytic, Enantioselective syn- Diamination of Alkenes
inferred← citeshttps://doi.org/10.1021/jacsau.5c01226openalex-snapshot
Synthesis of C sp 3 Chlorinated Compounds from Cyclopropanes, Olefins, and C–H Bonds via Photolysis of Willgerodt-Type Reagents
inferred← citeshttps://doi.org/10.1038/s41467-018-06763-4openalex-snapshot
A selenium-catalysed para-amination of phenols
inferred← citeshttps://doi.org/10.1038/s41467-021-24174-wopenalex-snapshot
Oxoammonium salts are catalysing efficient and selective halogenation of olefins, alkynes and aromatics
inferred← citeshttps://doi.org/10.1038/s41467-024-45991-9openalex-snapshot
Tuning light-driven oxidation of styrene inside water-soluble nanocages
inferred← citeshttps://doi.org/10.1038/s41467-024-47854-9openalex-snapshot
Catalytic 1,1-diazidation of alkenes
inferred← citeshttps://doi.org/10.1038/s41467-024-47942-wopenalex-snapshot
Stereospecific syn-dihalogenations and regiodivergent syn-interhalogenation of alkenes via vicinal double electrophilic activation strategy
inferred← citeshttps://doi.org/10.1038/s41557-024-01551-8openalex-snapshot
Repurposing of halogenated organic pollutants via alkyl bromide-catalysed transfer chlorination
inferred← citeshttps://doi.org/10.1038/s41557-024-01561-6openalex-snapshot
Diastereodivergent nucleophile–nucleophile alkene chlorofluorination
inferred← citeshttps://doi.org/10.1038/s41598-017-06892-8openalex-snapshot
Solid-State 77Se NMR of Organoselenium Compounds through Cross Polarization Magic Angle Spinning (CPMAS) Method
inferred← citeshttps://doi.org/10.1038/s41929-019-0398-0openalex-snapshot
DMSO-catalysed late-stage chlorination of (hetero)arenes
inferred← citeshttps://doi.org/10.1038/s42004-024-01365-2openalex-snapshot
Stereospecific syn-dichlorination of allylic amines enabled by identification of a superior stereo-directing group
inferred← citeshttps://doi.org/10.1038/s44160-026-01088-3openalex-snapshot
Electrophotocatalytic decarboxylative vicinal dichlorination of aliphatic carboxylic acids
inferred← citeshttps://doi.org/10.1038/s44160-026-01103-7openalex-snapshot
Electrophotocatalysis for direct vicinal dichlorination of carboxylic acids
inferred← citeshttps://doi.org/10.1039/bk9781839167386-00334openalex-snapshot
The Chemistry of Selenium-catalyzed Redox Processes
inferred← citeshttps://doi.org/10.1039/c5cc09753copenalex-snapshot
Catalytic insertion of aldehydes into dihalonitroacetophenones via sequential bond scission-aldol reaction-acyl transfer
inferred← citeshttps://doi.org/10.1039/c5cy01030fopenalex-snapshot
Recyclable (PhSe) 2 -catalyzed selective oxidation of isatin by H 2 O 2 : a practical and waste-free access to isatoic anhydride under mild and neutral conditions
inferred← citeshttps://doi.org/10.1039/c5cy01395jopenalex-snapshot
Organoselenium-catalyzed selectivity-switchable oxidation of β-ionone
inferred← citeshttps://doi.org/10.1039/c5cy01503kopenalex-snapshot
DMSO/iodine-catalyzed oxidative C–Se/C–S bond formation: a regioselective synthesis of unsymmetrical chalcogenides with nitrogen- or oxygen-containing arenes
inferred← citeshttps://doi.org/10.1039/c5qo00179jopenalex-snapshot
Organoselenium-catalyzed synthesis of indoles through intramolecular C–H amination
inferred← citeshttps://doi.org/10.1039/c6nj00658bopenalex-snapshot
Organoselenium-catalyzed vicinal dichlorination of unsaturated phosphonates
inferred← citeshttps://doi.org/10.1039/c6ob01306fopenalex-snapshot
Catalytic asymmetric bromochlorination of aromatic allylic alcohols promoted by multifunctional Schiff base ligands
inferred← citeshttps://doi.org/10.1039/c6ra20101fopenalex-snapshot
A simple and highly diasteroselective approach for the vicinal dichlorination of functional olefins
inferred← citeshttps://doi.org/10.1039/c6sc03012bopenalex-snapshot
Synthesis of malhamensilipin A exploiting iterative epoxidation/chlorination: experimental and computational analysis of epoxide-derived chloronium ions
inferred← citeshttps://doi.org/10.1039/c6ta02566hopenalex-snapshot
Design and preparation of a polymer resin-supported organoselenium catalyst with industrial potential
inferred← citeshttps://doi.org/10.1039/c7ob03177gopenalex-snapshot
Rose Bengal catalysed photo-induced selenylation of indoles, imidazoles and arenes: a metal free approach
inferred← citeshttps://doi.org/10.1039/c8cy01413bopenalex-snapshot
Fabrication of Se/C using carbohydrates as biomass starting materials: an efficient catalyst for regiospecific epoxidation of β-ionone with ultrahigh turnover numbers
inferred← citeshttps://doi.org/10.1039/c8gc01245hopenalex-snapshot
Visible-light-enabled oxyazidation of alkenes leading to α-azidoketones in air
inferred← citeshttps://doi.org/10.1039/c8ob01634hopenalex-snapshot
Electrophilic chloro(ω-alkoxy)lation of alkenes employing 1-chloro-1,2-benziodoxol-3-one: facile synthesis of β-chloroethers
inferred← citeshttps://doi.org/10.1039/c8ob02298dopenalex-snapshot
Selective alkyl ether cleavage by cationic bis(phosphine)iridium complexes
inferred← citeshttps://doi.org/10.1039/c8ob03160fopenalex-snapshot
Catalytic enantioselective iodolactonization reactions
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/c9ob00078jopenalex-snapshot
Synthesis, structural characterisation, and synthetic application of stable seleniranium ions
inferred← citeshttps://doi.org/10.1039/c9qo00620fopenalex-snapshot
Recent progress in selenium-catalyzed organic reactions
inferred← citeshttps://doi.org/10.1039/c9ra05004copenalex-snapshot
Copper-catalyzed direct C–H arylselenation of 4-nitro-pyrazoles and other heterocycles with selenium powder and aryl iodides. Access to unsymmetrical heteroaryl selenides
inferred← citeshttps://doi.org/10.1039/c9ra90098eopenalex-snapshot
Correction: Copper-catalyzed direct C–H arylselenation of 4-nitro-pyrazoles and other heterocycles with selenium powder and aryl iodides. Access to unsymmetrical heteroaryl selenides
inferred← citeshttps://doi.org/10.1039/c9sc05335bopenalex-snapshot
Selenophosphoramide-catalyzed diamination and oxyamination of alkenes
inferred← citeshttps://doi.org/10.1039/c9ta00846bopenalex-snapshot
A facile approach to constructing Pd@PCN–Se nano-composite catalysts for selective alcohol oxidation reactions
inferred← citeshttps://doi.org/10.1039/d0cy00400fopenalex-snapshot
Selenium-catalyzed oxidation of alkenes: insight into the mechanisms and developing trend
inferred← citeshttps://doi.org/10.1039/d0re00471eopenalex-snapshot
Synergetic catalysis of Se and Cu allowing diethoxylation of halomethylene ketones using O 2 as the mild oxidant
inferred← citeshttps://doi.org/10.1039/d2cc04030aopenalex-snapshot
Regioselective peri -C–H selenylation of aromatic compounds with weakly coordinating ketone groups
inferred← citeshttps://doi.org/10.1039/d2nj00159dopenalex-snapshot
p -Toluenesulfonic acid-catalyzed regioselective C4–H iodination of isoquinolin-1(2 H )-ones
inferred← citeshttps://doi.org/10.1039/d2nj02065copenalex-snapshot
Microwave assisted C–S cross-coupling reaction from thiols and 2-(4-bromo phenyl)-benzothiazole employed by CuI in acetonitrile
inferred← citeshttps://doi.org/10.1039/d2ob01597hopenalex-snapshot
HFIP-promoted halo-carbocyclizations of N - and O -tethered arene–alkene substrates to access all halo (X = Br, I, Cl)-functionalized tetrahydroquinoline and chroman cores
inferred← citeshttps://doi.org/10.1039/d3ob02012fopenalex-snapshot
Recent advances in oxidative chlorination
inferred← citeshttps://doi.org/10.1039/d3sc05231aopenalex-snapshot
Photocatalytic, modular difunctionalization of alkenes enabled by ligand-to-metal charge transfer and radical ligand transfer
inferred← citeshttps://doi.org/10.1039/d4ob01553copenalex-snapshot
Recent progress in the organoselenium-catalyzed difunctionalization of alkenes
inferred← citeshttps://doi.org/10.1039/d4ob01962hopenalex-snapshot
Dichlorination of olefins with trichloroisocyanuric acid (TCCA) and tetrabutylammonium chloride (TBACl)
inferred← citeshttps://doi.org/10.1039/d4qo01348dopenalex-snapshot
Recent advances in electrochemical difunctionalization of alkenes and alkynes for the synthesis of organohalides
inferred← citeshttps://doi.org/10.1039/d4sc00581copenalex-snapshot
Intramolecular chaperone-assisted dual-anchoring activation (ICDA): a suitable preorganization for electrophilic halocyclization
inferred← citeshttps://doi.org/10.1039/d5cc01542aopenalex-snapshot
Geminal homologative fluorination of carbonyl derivatives en route to 1-fluoro-2-haloethyl skeletons
inferred← citeshttps://doi.org/10.1039/d5cy00914fopenalex-snapshot
Efficient photoelectrocatalytic radical dichlorination of alkenes via synergism with Mn
inferred← citeshttps://doi.org/10.1039/d5gc00193eopenalex-snapshot
Deuterated methylselenylating reagents designed for diverse Se -methyl- d 3 scaffold construction
inferred← citeshttps://doi.org/10.1039/d5gc04102copenalex-snapshot
Metal-free electrohalogenation of olefins with aqueous NaX mediators
inferred← citeshttps://doi.org/10.1039/d5ob01253hopenalex-snapshot
Efficient synthesis of trifluoromethyl-containing vicinal chlorohydrins and dichlorides via Mn-mediated chlorohydroxylation and dichlorination of α-(trifluoromethyl)styrenes
inferred← citeshttps://doi.org/10.1039/d5qo00439jopenalex-snapshot
Visible light-mediated halofunctionalization of alkenes for the synthesis of vicinally functionalized organohalides
inferred← citeshttps://doi.org/10.1039/d6qo00047aopenalex-snapshot
Electrochemical vicinal dichlorination and dibromination of unactivated alkenes using TMSX as the halogen source
inferred← citeshttps://doi.org/10.1055/a-1684-0308openalex-snapshot
Halogenations of 3-Aryl-1H-pyrazol-5-amines
inferred← citeshttps://doi.org/10.1055/a-1961-6102openalex-snapshot
Catalytic Enantioselective Dihalogenation of Alkenes
inferred← citeshttps://doi.org/10.1055/a-2560-8048openalex-snapshot
N-Fluorobenzenesulfonimide-Mediated Oxidative Rearrangement of Tetrahydro-β-carbolines
inferred← citeshttps://doi.org/10.1055/s-0043-1763695openalex-snapshot
The Electrochemical trans-Chloroformyloxylation of Unactivated Alkenes
inferred← citeshttps://doi.org/10.1055/sos-sd-135-00173openalex-snapshot
35.1.5.1.12 Synthesis of 1-Chloro-n-Heteroatom-Functionalized Alkanes (n ≥2) by Addition across C=C Bonds (Update 2017)
inferred← citeshttps://doi.org/10.1055/sos-sd-225-00195openalex-snapshot
5.4 Halogenation and Halocyclization of Alkenes
inferred← citeshttps://doi.org/10.1080/00397911.2020.1774901openalex-snapshot
Dichlorination of olefins with diphenyl sulfoxide/oxalyl chloride
inferred← citeshttps://doi.org/10.1126/science.abf2974openalex-snapshot
Merging shuttle reactions and paired electrolysis for reversible vicinal dihalogenations
inferred← citeshttps://doi.org/10.1246/cl.210065openalex-snapshot
Selenium-catalyzed Functionalization of Alkynes
inferred← citeshttps://doi.org/10.12677/jocr.2023.114015openalex-snapshot
Recent Research Progress of Aromatic Halogenations with N-X Reagents
inferred← citeshttps://doi.org/10.12677/jocr.2024.122019openalex-snapshot
Recent Research Progress of Asymmetric Dihalogenation of Alkenes
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