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Organoselenium-Catalyzed Oxidative Allylic Fluorination with Electrophilic N–F Reagent
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1099-0690(199904)1999:4<797::aid-ejoc797>3.0.co;2-oopenalex-snapshot
Catalytic Oxyselenenylation–Deselenenylation Reactions of Alkenes – Stereoselective One-Pot Conversion of 3-Alkenols into 2,5-Dihydrofurans
inferredcites →https://doi.org/10.1002/(sici)1521-3897(200001)342:1<52::aid-prac52>3.0.co;2-hopenalex-snapshot
Synthesis of γ-Fluoro-α, β-unsaturated Carboxylic Esters from Saturated α-Fluoro Aldehydes
inferredcites →https://doi.org/10.1002/adsc.200800571openalex-snapshot
Eco‐Friendly Olefin Dihydroxylation Catalyzed by Diphenyl Diselenide
inferredcites →https://doi.org/10.1002/anie.200800222openalex-snapshot
Synthesis of 11 C, 18 F, 15 O, and 13 N Radiolabels for Positron Emission Tomography
inferredcites →https://doi.org/10.1002/anie.200903893openalex-snapshot
Green Chemistry with Selenium Reagents: Development of Efficient Catalytic Reactions
inferredcites →https://doi.org/10.1002/anie.201007307openalex-snapshot
Palladium‐Catalyzed Allylic Fluorination
inferredcites →https://doi.org/10.1002/anie.201203642openalex-snapshot
A Polycomponent Metal‐Catalyzed Aliphatic, Allylic, and Benzylic Fluorination
inferredcites →https://doi.org/10.1002/anie.201303662openalex-snapshot
Direct Oxidative Allylic and Vinylic Amination of Alkenes through Selenium Catalysis
inferredcites →https://doi.org/10.1002/anie.201610657openalex-snapshot
Organoselenium‐Catalyzed Regioselective C−H Pyridination of 1,3‐Dienes and Alkenes
inferredcites →https://doi.org/10.1002/chem.200400596openalex-snapshot
First Detection of a Selenenyl Fluoride ArSeF by NMR Spectroscopy: The Nature of Ar 2 Se 2 /XeF 2 and ArSeSiMe 3 /XeF 2 Reagents
inferredcites →https://doi.org/10.1002/chem.201406290openalex-snapshot
Selenium‐Catalyzed C(sp3)H Acyloxylation: Application in the Expedient Synthesis of Isobenzofuranones
inferredcites →https://doi.org/10.1002/ejoc.200801171openalex-snapshot
Recent Advances in Organoselenium Chemistry
inferredcites →https://doi.org/10.1002/ejoc.201000548openalex-snapshot
Dehydrogenative Functionalization of C(sp3)–H Bonds Adjacent to a Heteroatom Mediated by Oxoammonium Salts
inferredcites →https://doi.org/10.1002/ejoc.201402049openalex-snapshot
Direct Allylic Functionalization Through Pd‐Catalyzed C–H Activation
inferredcites →https://doi.org/10.1007/s11426-015-5387-9openalex-snapshot
Advances and challenges in palladium-catalyzed intermolecular selective allylic C-H functionalization of alkenes
inferredcites →https://doi.org/10.1016/j.tet.2008.12.068openalex-snapshot
Electrochemical fluoro-selenenylation of electron-deficient olefins
inferredcites →https://doi.org/10.1016/j.tet.2012.08.078openalex-snapshot
Stereoselective selenium catalyzed dihydroxylation and hydroxymethoxylation of alkenes
inferredcites →https://doi.org/10.1016/j.tetlet.2009.01.052openalex-snapshot
Synthesis of aryl allylic fluorides by direct electrophilic fluorination of alkenes
inferredcites →https://doi.org/10.1016/j.tetlet.2010.08.090openalex-snapshot
Selectfluor-promoted fluorination of piperidinyl olefins
inferredcites →https://doi.org/10.1016/j.tetlet.2014.05.093openalex-snapshot
A cooperative allylic fluorination: combination of nucleophilic and electrophilic fluorine sources
inferredcites →https://doi.org/10.1016/s0013-4686(97)85474-6openalex-snapshot
Electrochemical generation of [PhSeF] for fluoro-selenation of alkenes and alkynes and its recycle use
inferredcites →https://doi.org/10.1016/s0022-1139(98)00115-8openalex-snapshot
Substituent effects on the regioselectivity in fluorination of allylic alcohols with DAST
inferredcites →https://doi.org/10.1016/s0022-1139(99)00282-1openalex-snapshot
Reactions of benzeneselenenyl fluoride generated by XeF2-(PhSe)2 system with electron-deficient alkenes
inferredcites →https://doi.org/10.1016/s0022-328x(00)00325-9openalex-snapshot
Fluoro-functionalization mediated by the reactive chalcogen reagents
inferredcites →https://doi.org/10.1016/s0040-4020(01)96722-5openalex-snapshot
N-phenylselenophthalimide (NPSP)
inferredcites →https://doi.org/10.1016/s0040-4039(00)94406-xopenalex-snapshot
A new synthesis of 2-fluoro-1-olefins
inferredcites →https://doi.org/10.1016/s0040-4039(00)94448-4openalex-snapshot
Benzeneselenenyl fluoride equivalent in situ generated with XeF2-(PhSe)2 in Ch2Cl2 for fluoroselenenylation of olefins
inferredcites →https://doi.org/10.1021/acs.chemrev.6b00657openalex-snapshot
Organocatalysis in Inert C–H Bond Functionalization
inferredcites →https://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
inferredcites →https://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
inferredcites →https://doi.org/10.1021/acs.orglett.5b03543openalex-snapshot
Organoselenium-Catalyzed Synthesis of Oxygen- and Nitrogen-Containing Heterocycles
inferredcites →https://doi.org/10.1021/acscatal.7b01216openalex-snapshot
Oxidative Alkene Functionalizations via Selenium-π-Acid Catalysis
inferredcites →https://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
inferredcites →https://doi.org/10.1021/cr068410eopenalex-snapshot
The Chemistry of Propargylic and Allylic Fluorides
inferredcites →https://doi.org/10.1021/cr500706aopenalex-snapshot
Monofluorination of Organic Compounds: 10 Years of Innovation
inferredcites →https://doi.org/10.1021/ja00405a064openalex-snapshot
Generation and recycle use of selenenylating reagents in electrochemical oxyselenenylation-deselenenylation of olefins
inferredcites →https://doi.org/10.1021/ja206960kopenalex-snapshot
Palladium-Catalyzed Regio- and Enantioselective Fluorination of Acyclic Allylic Halides
inferredcites →https://doi.org/10.1021/ja2087213openalex-snapshot
Iridium-Catalyzed Allylic Fluorination of Trichloroacetimidates
inferredcites →https://doi.org/10.1021/ja407223gopenalex-snapshot
Palladium-Catalyzed Allylic C–H Fluorination
inferredcites →https://doi.org/10.1021/ja407410bopenalex-snapshot
Asymmetric Cross-Dehydrogenative Coupling Enabled by the Design and Application of Chiral Triazole-Containing Phosphoric Acids
inferredcites →https://doi.org/10.1021/ja507468uopenalex-snapshot
An In Situ Directing Group Strategy for Chiral Anion Phase-Transfer Fluorination of Allylic Alcohols
inferredcites →https://doi.org/10.1021/jacs.5b07492openalex-snapshot
Iridium-Catalyzed Enantioselective Fluorination of Racemic, Secondary Allylic Trichloroacetimidates
inferredcites →https://doi.org/10.1021/jacs.6b00356openalex-snapshot
Enantiodivergent Fluorination of Allylic Alcohols: Data Set Design Reveals Structural Interplay between Achiral Directing Group and Chiral Anion
inferredcites →https://doi.org/10.1021/jacs.6b01462openalex-snapshot
A Chiral Electrophilic Selenium Catalyst for Highly Enantioselective Oxidative Cyclization
inferredcites →https://doi.org/10.1021/jm800219fopenalex-snapshot
The Many Roles for Fluorine in Medicinal Chemistry
inferredcites →https://doi.org/10.1021/jo00302a012openalex-snapshot
Selenium-catalyzed conversion of methyl ketones into .alpha.-keto acetals
inferredcites →https://doi.org/10.1021/jo00893a007openalex-snapshot
New fluorinating reagents. Dialkylaminosulfur fluorides
inferredcites →https://doi.org/10.1021/jo01337a046openalex-snapshot
Selenium-catalyzed nonradical chlorination of olefins with N-chlorosuccinimide
inferredcites →https://doi.org/10.1021/jo01337a047openalex-snapshot
Conversion of allylic phenylselenides to the rearranged allylic chlorides by N-chlorosuccinimide. Mechanism of selenium-catalyzed allylic chlorination of .beta.-pinene
inferredcites →https://doi.org/10.1021/jo800634ropenalex-snapshot
Oxidative Rearrangement of Tertiary Allylic Alcohols Employing Oxoammonium Salts
inferredcites →https://doi.org/10.1021/jo902144bopenalex-snapshot
Oxidative Cleavage of Benzylic and Related Ethers, Using an Oxoammonium Salt
inferredcites →https://doi.org/10.1021/ol036525oopenalex-snapshot
Selective Selenocatalytic Allylic Chlorination
inferredcites →https://doi.org/10.1021/ol071223yopenalex-snapshot
Catalytic Use of Selenium Electrophiles in Cyclizations
inferredcites →https://doi.org/10.1021/ol202800kopenalex-snapshot
Selenium-Catalyzed Regioselective Cyclization of Unsaturated Carboxylic Acids Using Hypervalent Iodine Oxidants
inferredcites →https://doi.org/10.1021/ol500075hopenalex-snapshot
Organoselenium-Catalyzed Mild Dehydration of Aldoximes: An Unexpected Practical Method for Organonitrile Synthesis
inferredcites →https://doi.org/10.1038/nchem.2141openalex-snapshot
Catalytic, stereospecific syn-dichlorination of alkenes
inferredcites →https://doi.org/10.1039/c1cs15104eopenalex-snapshot
Recent advances in transition metal-catalyzed sp3C–H amination adjacent to double bonds and carbonyl groups
inferredcites →https://doi.org/10.1039/c2cc16158copenalex-snapshot
Transition metal catalysis and nucleophilic fluorination
inferredcites →https://doi.org/10.1039/c39810000511openalex-snapshot
A novel synthesis of α- and γ- fluoroalkylphosphonates
inferredcites →https://doi.org/10.1039/c39920001165openalex-snapshot
Catalytic conversion of alkenes into allylic ethers and esters using diselenides having internal tertiary amines
inferredcites →https://doi.org/10.1039/c39930000637openalex-snapshot
Catalytic conversion of (β,γ-unsaturated esters, amides and nitriles into γ-alkoxy or γ-hydroxy α,β-unsaturated derivatives induced by persulfate anion oxidation of diphenyl diselenide
inferredcites →https://doi.org/10.1039/c5qo00179jopenalex-snapshot
Organoselenium-catalyzed synthesis of indoles through intramolecular C–H amination
inferredcites →https://doi.org/10.1039/c7re00083aopenalex-snapshot
Selective continuous flow synthesis of hydroxy lactones from alkenoic acids
inferredcites →https://doi.org/10.1055/s-2004-829073openalex-snapshot
Alkoxyamines by Reaction of 2,2,6,6-Tetramethylpiperidine-1-oxoammonium Tetrafluoroborate with Enolates
inferredcites →https://doi.org/10.1055/s-2004-832827openalex-snapshot
Phenylselenofluorination of Alkenes and Alkynes Promoted by Difluoroiodotoluene and Diphenyldiselenide
inferredcites →https://doi.org/10.1055/s-2005-923585openalex-snapshot
Electrochemical Generation and Catalytic Use of Selenium Electrophiles
inferredcites →https://doi.org/10.1073/pnas.1304346110openalex-snapshot
A combination of directing groups and chiral anion phase-transfer catalysis for enantioselective fluorination of alkenes
inferredcites →https://doi.org/10.1246/bcsj.77.2203openalex-snapshot
Electron-Transfer Kinetics of Nitroxide Radicals as an Electrode-Active Material
inferredcites →https://doi.org/10.2174/138527210793358231openalex-snapshot
Organoselenium Compounds as Catalysts in Nature and Laboratory
inferredcites →https://doi.org/10.3390/molecules22050835openalex-snapshot
Electrophilic Selenium Catalysis with Electrophilic N-F Reagents as the Oxidants
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4814372openalex-extracted
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
inferred← citeshttps://doi.org/10.1002/047084289x.rn01221openalex-snapshot
1-Fluoro-2,4,6-trimethylpyridinium Tetrafluoroborate
inferred← citeshttps://doi.org/10.1002/047084289x.rn01221.pub2openalex-snapshot
1‐Fluoro‐2,4,6‐trimethylpyridinium Tetrafluoroborate
inferred← citeshttps://doi.org/10.1002/adsc.201801163openalex-snapshot
Iron‐Enabled Utilization of Air as the Terminal Oxidant Leading to Aerobic Oxidative Deoximation by Organoselenium Catalysis
inferred← citeshttps://doi.org/10.1002/adsc.202001006openalex-snapshot
Ag‐Catalyzed Cyclization of Arylboronic Acids with Elemental Selenium for the Synthesis of Selenaheterocycles
inferred← citeshttps://doi.org/10.1002/adsc.202101227openalex-snapshot
Synthesis of Organoselenium Compounds with Elemental Selenium
inferred← citeshttps://doi.org/10.1002/ajoc.202200381openalex-snapshot
PIFA Induced Regioselective C‐H Chalcogenylation of Benzo[d]imidazo[5,1‐b]thiazoles under Mild Conditions
inferred← citeshttps://doi.org/10.1002/ange.201915470openalex-snapshot
Enantioselective Construction of Axially Chiral Amino Sulfide Vinyl Arenes by Chiral Sulfide‐Catalyzed Electrophilic Carbothiolation of Alkynes
inferred← citeshttps://doi.org/10.1002/ange.202100801openalex-snapshot
Redox‐Neutrale Selen‐katalysierte Isomerisierung von para ‐Hydroxamsäuren zu para ‐Aminophenolen
inferred← citeshttps://doi.org/10.1002/ange.6267376openalex-snapshot
Cobalt‐Catalyzed Enantioselective Vinyl Carbene Annulation: A Versatile Platform for Semisaturated Heterocycles
inferred← citeshttps://doi.org/10.1002/anie.201915470openalex-snapshot
Enantioselective Construction of Axially Chiral Amino Sulfide Vinyl Arenes by Chiral Sulfide‐Catalyzed Electrophilic Carbothiolation of Alkynes
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.6267376openalex-snapshot
Cobalt‐Catalyzed Enantioselective Vinyl Carbene Annulation: A Versatile Platform for Semisaturated Heterocycles
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/celc.201901525openalex-snapshot
Recent Advances in Electrochemical Chalcogen (S/Se)‐Functionalization of Organic Molecules
inferred← citeshttps://doi.org/10.1002/ejoc.202001673openalex-snapshot
Synthesis of Aminoallenes via Selenium‐π‐Acid‐Catalyzed Cross‐Coupling of N‐Fluorinated Sulfonimides with Simple Alkynes
inferred← citeshttps://doi.org/10.1002/ejoc.202401162openalex-snapshot
Recent Advances in Allylic Fluoride Synthesis
inferred← citeshttps://doi.org/10.1007/s00214-019-2417-2openalex-snapshot
Fluorination of benzene with disubstituted N-fluoropyridinium salts in acetonitrile solution: 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/10.1016/b978-0-12-409547-2.14760-2openalex-snapshot
Three-Membered Rings With One Selenium or Tellurium Atom
inferred← citeshttps://doi.org/10.1016/b978-0-12-812958-6.00007-0openalex-snapshot
Fluorination of Allylic Positions Toward the Synthesis of Fluorinated Bioactive Compounds
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00002-8openalex-snapshot
Synthesis of Fluorides
inferred← citeshttps://doi.org/10.1016/j.catcom.2019.105730openalex-snapshot
Selenium-doped carbon: An unexpected efficient solid acid catalyst for Beckmann rearrangement of ethyl 2-(2-aminothiazole-4-yl)-2-hydroxyiminoacetate
inferred← citeshttps://doi.org/10.1016/j.cclet.2019.01.012openalex-snapshot
Recent advances on deoximation: From stoichiometric reaction to catalytic reaction
inferred← citeshttps://doi.org/10.1016/j.cclet.2020.07.031openalex-snapshot
An unexpected generation of magnetically separable Se/Fe3O4 for catalytic degradation of polyene contaminants with molecular oxygen
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.118390openalex-snapshot
Leishmanicidal and trypanocidal potential of ß,γ-unsaturated carboxylic acid synthetic derivatives
inferred← citeshttps://doi.org/10.1016/j.isci.2026.115123openalex-snapshot
Selenium-catalyzed organic transformations
inferred← citeshttps://doi.org/10.1016/j.jscs.2023.101796openalex-snapshot
Synthesis and biological evaluation of selenopyrimidine derivatives bearing thiazolyl moiety
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.molliq.2022.119907openalex-snapshot
Novel organoselenium-based N-mealanilic acid and its zinc (II) chelate: Catalytic, anticancer, antimicrobial, antioxidant, and computational assessments
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.136940openalex-snapshot
Photo-induced organoselenium-catalyzed synthesis of 2-substituted quinazoline derivatives
inferred← citeshttps://doi.org/10.1016/j.scib.2019.07.007openalex-snapshot
Organotellurium catalysis-enabled utilization of molecular oxygen as oxidant for oxidative deoximation reactions under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154197openalex-snapshot
Regioselective transformation of terminal and internal alkynes into α,α-difluoro ketones under mild conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154255openalex-snapshot
Metal-free synthesis of diselenides and ditellurides by using TMSCN
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154825openalex-snapshot
Visible-Light-Induced decarboxylative selenation of N-Hydroxyphthalimide esters with diselenides to unsymmetrical monoselenides
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.2c01907openalex-snapshot
Copper(I)-Catalyzed Three-Component Selenosulfonation of Maleimides with Sulfonyl Hydrazides and Diselenides via Radical Relay
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00788openalex-snapshot
Oxidative Three-Component Selenofunctionalization of Alkenes: Convenient Access to Vicinally Functionalized Selenides
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00622openalex-snapshot
Organoselenium-Catalyzed C2,3-Diarylation of N–H Indoles
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01294openalex-snapshot
Organoselenium Accelerated Bromolactonization Reaction
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01808openalex-snapshot
Chemoselective Mono- and Difluorination of 1,3-Dicarbonyl Compounds
inferred← citeshttps://doi.org/10.1021/acs.joc.9b03275openalex-snapshot
Lewis Base/Brønsted Acid Cocatalysis for Thiocyanation of Amides and Thioamides
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Catalytic Wacker Oxidation of Tetrasubstituted Alkenes: Efficient Access to gem -Dimethyl Ketones
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01200openalex-snapshot
Stereospecific Isomerization of Allylic Halides via Ion Pairs with Induced Noncovalent Chirality
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Organoseleno-Catalyzed Synthesis of α,β-Unsaturated α′-Alkoxy Ketones from Allenes Enabled by Se···O Interactions
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Selenium-Catalyzed Trifluoromethylsulfinylation/Rearrangement of Allylic and Propargylic Alcohols: Access to Allylic and Allenic Triflones
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Organoselenium-Catalyzed Cross-Dehydrogenative Coupling of Alkenes and Azlactones
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Chemoselective Synthesis of α-Halo-α,α-difluoromethyl Ketones from Trimethyl(phenylethynyl)silane
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04012openalex-snapshot
Visible-Light-Induced Monofluoromethylation of Styrenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c03173openalex-snapshot
Formal Total Synthesis of (±)-Isoalantolactone
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Advances in Nucleophilic Allylic Fluorination
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Regio-, Site-, and Stereoselective Three-Component Aminofluorination of 1,3-Dienes via Cooperative Silver Salt and Copper Catalysis
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Selenium-π-Acid Catalyzed Oxidative Functionalization of Alkynes: Facile Access to Ynones and Multisubstituted Oxazoles
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Access to Diverse Seleno-spirocyclohexadienones via Ag(II)-Catalyzed Selenylative ipso-Annulation with Se and Boronic Acids
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Cobalt-Catalyzed Double Carbonylation of Cyclopropenes through a Stereodivergent β-Alkenyl Ketene Pathway
inferred← citeshttps://doi.org/10.1038/s41467-021-27165-zopenalex-snapshot
A general strategy for C(sp3)–H functionalization with nucleophiles using methyl radical as a hydrogen atom abstractor
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Catalytic 1,1-diazidation of alkenes
inferred← citeshttps://doi.org/10.1039/bk9781839167386-00334openalex-snapshot
The Chemistry of Selenium-catalyzed Redox Processes
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/c8qo00909kopenalex-snapshot
Acid-catalyzed oxidative cleavage of S–S and Se–Se bonds with DEAD: efficient access to sulfides and selenides
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/c9qo00620fopenalex-snapshot
Recent progress in selenium-catalyzed organic reactions
inferred← citeshttps://doi.org/10.1039/c9qo01497gopenalex-snapshot
Chelation-assisted transition metal-catalysed C–H chalcogenylations
inferred← citeshttps://doi.org/10.1039/c9se00850kopenalex-snapshot
Concise synthesis of polyselenides: efficient catalysts for the oxidative cracking reaction of alkenes allowing the utilization of O 2 as a partial oxidant under mild conditions
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/d0cc07264hopenalex-snapshot
Photo-induced energy transfer relay of N-heterocyclic carbene catalysis: an asymmetric α-fluorination/isomerization cascade
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/d0ra06016jopenalex-snapshot
Synthesis of selenated isochromenones by AgNO 3 -catalyzed three-component reaction of alkynylaryl esters, selenium powder and ArB(OH) 2
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/d2qo00074aopenalex-snapshot
Direct access to α,α-chlorofluoro arylketones via mild electrophilic heterohalogenation of arylalkynes
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/d2sc00968dopenalex-snapshot
Catalytic alkene skeletal modification for the construction of fluorinated tertiary stereocenters
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/d5gc01259gopenalex-snapshot
Electrochemical vicinal amidoselenation of unactivated olefins via a tandem Ritter reaction
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/10.2174/1570179419666211224144932openalex-snapshot
Transition Metal Catalyst, Solvent, Base Free Synthesis of Diaryl Diselenides under Mechanical Ball Milling
inferred← citeshttps://doi.org/10.26434/chemrxiv.13644218openalex-snapshot
A General Strategy for C(sp3)–H Functionalization with Nucleophiles Using Methyl Radical as a Hydrogen Atom Abstractor
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/catal12020233openalex-snapshot
Tetramethylammonium Fluoride: Fundamental Properties and Applications in C-F Bond-Forming Reactions and as a Base
inferred← citeshttps://doi.org/10.3390/molecules28186614openalex-snapshot
Recent Advances in the Use of Diorganyl Diselenides as Versatile Catalysts
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/10.3762/bjoc.16.208openalex-snapshot
Synthesis of novel fluorinated building blocks via halofluorination and related reactions
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.79.910openalex-snapshot
Fluorination -A Decade of Progress (2010-2020)
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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