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Cobalt-Catalyzed Heck-Type Reaction of Alkyl Halides with Styrenes
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9783527612222openalex-snapshot
Metal‐Catalyzed Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1016/0022-328x(88)80484-4openalex-snapshot
Condensation of organic bromides with vinyl compounds catalysed by nickel complexes in the presence of zinc
inferredcites →https://doi.org/10.1016/s0040-4039(01)81080-7openalex-snapshot
Palladium-catalyzed acylation of activated alkenes with bridgehead acid chlorides
inferredcites →https://doi.org/10.1021/cr9903048openalex-snapshot
The Heck Reaction as a Sharpening Stone of Palladium Catalysis
inferredcites →https://doi.org/10.1021/jo981930sopenalex-snapshot
Adjusting the Top End of the Alkyl Radical Kinetic Scale. Laser Flash Photolysis Calibrations of Fast Radical Clocks and Rate Constants for Reactions of Benzeneselenol
inferredcites →https://doi.org/10.1246/bcsj.44.581openalex-snapshot
Arylation of Olefin with Aryl Iodide Catalyzed by Palladium
inferredcites →https://doi.org/10.5059/yukigoseikyokaishi.59.1044openalex-snapshot
Titanocene-Catalyzed Reaction of Alkenes and Dienes with Alkyl Halides and Chlorosilanes.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Trimethylsilylmethylmagnesium Chloride
inferred← citeshttps://doi.org/10.1002/047084289x.rt322.pub3openalex-snapshot
Trimethylsilylmethylmagnesium Chloride
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Cobalt‐Catalyzed Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9780470842898.rt322.pub2openalex-snapshot
Trimethylsilylmethylmagnesium Chloride
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Cobaltous chloride
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inferred← citeshttps://doi.org/10.1002/ange.200500255openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201307069openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201311323openalex-snapshot
Palladium‐Catalyzed Heck‐Type Cross‐Couplings of Unactivated Alkyl Iodides
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inferred← citeshttps://doi.org/10.1002/ange.201707181openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201813689openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201906075openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200500255openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200500576openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200702528openalex-snapshot
Ni‐Catalyzed Cascade Formation of C(sp3)C(sp3) Bonds by Cyclization and Cross‐Coupling Reactions of Iodoalkanes with Alkyl Zinc Halides
inferred← citeshttps://doi.org/10.1002/anie.200803611openalex-snapshot
Secondary Alkyl Halides in Transition‐Metal‐Catalyzed Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/anie.201106110openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201108350openalex-snapshot
Nickel‐Catalyzed Heck‐Type Alkenylation of Secondary and Tertiary α‐Carbonyl Alkyl Bromides
inferred← citeshttps://doi.org/10.1002/anie.201307069openalex-snapshot
Nickel‐Catalyzed Sonogashira Reactions of Non‐activated Secondary Alkyl Bromides and Iodides
inferred← citeshttps://doi.org/10.1002/anie.201311323openalex-snapshot
Palladium‐Catalyzed Heck‐Type Cross‐Couplings of Unactivated Alkyl Iodides
inferred← citeshttps://doi.org/10.1002/anie.201402893openalex-snapshot
Palladium‐Catalyzed Oxidative Difunctionalization of Alkenes with α‐Carbonyl Alkyl Bromides Initiated through a Heck‐type Insertion: A Route to Indolin‐2‐ones
inferred← citeshttps://doi.org/10.1002/anie.201408341openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201410176openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201707181openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201813689openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201906075openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.200802483openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201803642openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.202200465openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/zaac.200700206openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/128_2011_261openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.adomc.2018.02.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.catcom.2009.01.018openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.catcom.2015.12.027openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ccr.2004.05.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ccr.2017.10.012openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ica.2014.11.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.inoche.2019.107470openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.isci.2018.04.020openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jorganchem.2014.12.033openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jorganchem.2020.121354openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jorganchem.2021.122207openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jorganchem.2025.123953openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molcata.2004.11.011openalex-snapshot
Heck coupling by Pd deposited onto organic–inorganic hybrid supports
inferred← citeshttps://doi.org/10.1016/j.poly.2013.06.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.snb.2016.09.126openalex-snapshot
Selective imaging of Co 2+ in live cells with a “turn-on” fluorescent probe
inferred← citeshttps://doi.org/10.1016/j.tet.2007.12.047openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2009.10.050openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2019.06.034openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.08.025openalex-snapshot
Regioselective cross-coupling of allylindium reagents with activated benzylic bromides—a simple and efficient procedure for the synthesis of terminal alkenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.07.060openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.09.150openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.09.092openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.09.042openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151283openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4020(03)00404-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(03)01377-7openalex-snapshot
Palladium-catalyzed Heck-type reaction of 2-chloro acetamides with olefins
inferred← citeshttps://doi.org/10.1021/acs.accounts.9b00044openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.0c02834openalex-snapshot
Iminyl-Radical-Promoted C–C Bond Cleavage/Heck-Like Coupling via Dual Cobaloxime and Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00047openalex-snapshot
Regioselective Synthetic Approach to Higher Alkenes from Lower Alkenes with Sulfoxides in the Fe3+/H2O2 System via Direct Alkylation or Arylation of the Csp2–H Bond on the C═C Bond of Alkenes
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01002openalex-snapshot
Synthesis of α-Bromo Arylethyl Sulfonyl Fluorides and β-Arylethenesulfonyl Fluorides via Copper-Catalyzed Meerwein Arylation
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02279openalex-snapshot
Nickel-Catalyzed Benzylation of Aryl Alkenes with Benzylamines via C–N Bond Activation
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00898openalex-snapshot
Ruthenium-Catalyzed Heck-Type Alkenylation of Alkyl Bromides
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00224openalex-snapshot
Radical Aza-Cyclization of α-Imino-oxy Acids for Synthesis of Alkene-Containing N-Heterocycles via Dual Cobaloxime and Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00963openalex-snapshot
Directing-Group-Based Strategy Enabling Intermolecular Heck-Type Reaction of Cycloketone Oxime Esters and Unactivated Alkenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01417openalex-snapshot
Correction to “Radical Aza-Cyclization of α-Imino-oxy Acids for Synthesis of Alkene-Containing N-Heterocycles via Dual Cobaloxime and Photoredox Catalysis”
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01557openalex-snapshot
Cobalt-Bisoxazoline-Catalyzed Enantioselective Cross-Coupling of α-Bromo Esters with Alkenyl Grignard Reagents
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02742openalex-snapshot
Visible-Light-Promoted Intramolecular α-Allylation of Aldehydes in the Absence of Sacrificial Hydrogen Acceptors
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03676openalex-snapshot
Photoinduced Cobalt Catalyzed Radical Heck-Type Reaction of Alkyl Electrophiles
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02294openalex-snapshot
Fe-Catalyzed Reductive Coupling of Unactivated Alkenes with β-Nitroalkenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02482openalex-snapshot
Synthesis ofE-Alkyl Alkenes from Terminal Alkynes via Ni-Catalyzed Cross-Coupling of Alkyl Halides with B-Alkenyl-9-borabicyclo[3.3.1]nonanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03608openalex-snapshot
KIO 3 -Catalyzed Aerobic Cross-Coupling Reactions of Enaminones and Thiophenols: Synthesis of Polyfunctionalized Alkenes by Metal-Free C–H Sulfenylation
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03349openalex-snapshot
Cobalt-Catalyzed C(sp2)–C(sp3) Cross-Coupling Reactions of Diarylmanganese Reagents with Secondary Alkyl Iodides
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03289openalex-snapshot
Photoinduced, Copper-Promoted Regio- and Stereoselective Decarboxylative Alkylation of α,β-Unsaturated Acids with Alkyl Iodides
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03591openalex-snapshot
Heck Reaction of Electronically Diverse Tertiary Alkyl Halides
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00023openalex-snapshot
Irradiation-Induced Palladium-Catalyzed Decarboxylative Heck Reaction of Aliphatic N -(Acyloxy)phthalimides at Room Temperature
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01600openalex-snapshot
Regioselective Copper-Catalyzed Oxidative Coupling of α-Alkylated Styrenes with Tertiary Alkyl Radicals
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01962openalex-snapshot
[4 + 2] Annulation Cascades of 2-Bromo-1-arylpropan-1-ones with Terminal Alkynes Involving C–Br/C–H Functionalization
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b04024openalex-snapshot
Iron(II)-Catalyzed Heck-Type Coupling of Vinylarenes with Alkyl Iodides
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00142openalex-snapshot
Divergent C–H Oxidative Radical Functionalization of Olefins to Install Tertiary Alkyl Motifs Enabled by Copper Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03189openalex-snapshot
Copper-Catalyzed Three-Component Cascade Michael Addition/Heck-Type Alkylation/Annulation: Accessing Fully Substituted 1,3-Dihydro-2H-pyrrol-2-ones
inferred← citeshttps://doi.org/10.1021/acscatal.1c04748openalex-snapshot
Controlling Non-Native Cobalamin Reactivity and Catalysis in the Transcription Factor CarH
inferred← citeshttps://doi.org/10.1021/acscatal.2c00173openalex-snapshot
Tuning Redox States of Phenalenyl-Based Molecules by Consecutive Reduction toward Transition Metal-Free Heck-Type C–C Cross-Coupling
inferred← citeshttps://doi.org/10.1021/acscatal.3c01763openalex-snapshot
Anion-Tuning of Organozincs Steering Cobalt-Catalyzed Radical Relay Couplings
inferred← citeshttps://doi.org/10.1021/acscatal.6b03287openalex-snapshot
Iron-Catalyzed Heck-Type Alkenylation of Functionalized Alkyl Bromides
inferred← citeshttps://doi.org/10.1021/acscatal.6c02584openalex-snapshot
Cobalt Metallaphotoredox Catalysis Enabled Alkyl Heck-Type Reaction of Alcohols and 1-Hydroxycarbohydrates
inferred← citeshttps://doi.org/10.1021/cr100198wopenalex-snapshot
Direct C−H Transformation via Iron Catalysis
inferred← citeshttps://doi.org/10.1021/cr3002966openalex-snapshot
Mixed AggregAte (MAA): A Single Concept for All Dipolar Organometallic Aggregates. 2. Syntheses and Reactivities of Homo/HeteroMAAs
inferred← citeshttps://doi.org/10.1021/cr9000786openalex-snapshot
Cobalt-Catalyzed Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/ja026317bopenalex-snapshot
Palladium-Catalyzed Intramolecular Oxidative Alkylation of Unactivated Olefins
inferred← citeshttps://doi.org/10.1021/ja204982wopenalex-snapshot
Cobalt-Catalyzed Hydroalkylation of [60]Fullerene with Active Alkyl Bromides: Selective Synthesis of Monoalkylated Fullerenes
inferred← citeshttps://doi.org/10.1021/ja2084509openalex-snapshot
Mild and Efficient Nickel-Catalyzed Heck Reactions with Electron-Rich Olefins
inferred← citeshttps://doi.org/10.1021/ja211272vopenalex-snapshot
Copper-Catalyzed Enantioselective Intramolecular Alkene Amination/Intermolecular Heck-Type Coupling Cascade
inferred← citeshttps://doi.org/10.1021/ja409661nopenalex-snapshot
An Efficient Generation of a Functionalized Tertiary-Alkyl Radical for Copper-catalyzed Tertiary-Alkylative Mizoroki-Heck type Reaction
inferred← citeshttps://doi.org/10.1021/ja5026485openalex-snapshot
Enantiospecific Intramolecular Heck Reactions of Secondary Benzylic Ethers
inferred← citeshttps://doi.org/10.1021/jacs.6c01895openalex-snapshot
Visible-Light-Induced C–S Bond Cleavage Enables Alkyl Radical Generation from Redox-Inert Substrates
inferred← citeshttps://doi.org/10.1021/jacs.6c06343openalex-snapshot
Ligand-Modulated Cobalt-Catalyzed Alkene Carbocarbonylation Unlocks Aliphatic Ketone Synthesis
inferred← citeshttps://doi.org/10.1021/jacs.7b10009openalex-snapshot
Irradiation-Induced Heck Reaction of Unactivated Alkyl Halides at Room Temperature
inferred← citeshttps://doi.org/10.1021/jacs.8b08605openalex-snapshot
Ti-Catalyzed Radical Alkylation of Secondary and Tertiary Alkyl Chlorides Using Michael Acceptors
inferred← citeshttps://doi.org/10.1021/jacs.8b10874openalex-snapshot
Directed Copper-Catalyzed Intermolecular Heck-Type Reaction of Unactivated Olefins and Alkyl Halides
inferred← citeshttps://doi.org/10.1021/jacs.9b06920openalex-snapshot
Cobaloxime Catalysis: Selective Synthesis of Alkenylphosphine Oxides under Visible Light
inferred← citeshttps://doi.org/10.1021/jo049506gopenalex-snapshot
Cobalt-Catalyzed Regioselective Carbocyclization Reaction of o-Iodophenyl Ketones and Aldehydes with Alkynes, Acrylates, and Acrylonitrile: A Facile Route to Indenols and Indenes
inferred← citeshttps://doi.org/10.1021/jo052250+openalex-snapshot
Iron−Phosphine, −Phosphite, −Arsine, and −Carbene Catalysts for the Coupling of Primary and Secondary Alkyl Halides with Aryl Grignard Reagents
inferred← citeshttps://doi.org/10.1021/jo0617013openalex-snapshot
Suzuki−Miyaura Cross-Coupling Reactions of Potassium Vinyltrifluoroborate with Aryl and Heteroaryl Electrophiles
inferred← citeshttps://doi.org/10.1021/ol035514sopenalex-snapshot
Cobalt-Catalyzed Carbocyclization of o-Iodobenzaldehydes and o-Iodophenylketones with Alkynes
inferred← citeshttps://doi.org/10.1021/ol0356643openalex-snapshot
Cobalt-Catalyzed Three-Component Coupling Reaction of Alkyl Halides, 1,3-Dienes, and Trimethylsilylmethylmagnesium Chloride
inferred← citeshttps://doi.org/10.1021/ol0529142openalex-snapshot
Cobalt(II)-Catalyzed Cross-Coupling between Polyfunctional Arylcopper Reagents and Aryl Fluorides or Tosylates
inferred← citeshttps://doi.org/10.1021/ol101777xopenalex-snapshot
Cobalt-Catalyzed Addition of Azoles to Alkynes
inferred← citeshttps://doi.org/10.1021/ol401876nopenalex-snapshot
Co-Catalyzed Radical Cycloaddition of [60]Fullerene with Active Dibromides: Selective Synthesis of Carbocycle-Fused Fullerene Monoadducts
inferred← citeshttps://doi.org/10.1021/ol5004687openalex-snapshot
Co-Catalyzed Synthesis of 1,4-Dicarbonyl Compounds Using TBHP Oxidant
inferred← citeshttps://doi.org/10.1021/ol503744aopenalex-snapshot
Cobalt-Catalyzed Cross-Dehydrogenative Coupling Reaction in Water by Visible Light
inferred← citeshttps://doi.org/10.1021/ol702449mopenalex-snapshot
A Concise and Efficient Synthesis of (−)-Allosamizoline
inferred← citeshttps://doi.org/10.1021/om034067hopenalex-snapshot
Comparing Nickel- and Palladium-Catalyzed Heck Reactions
inferred← citeshttps://doi.org/10.1021/om7008793openalex-snapshot
Cyclometalation Reactions Involving C−Cl Bond Activation of ortho-Chlorinated Substrates with Imine as Anchoring Groups by Cobalt Complexes
inferred← citeshttps://doi.org/10.1038/s41467-019-08631-1openalex-snapshot
Direct dehydrogenative alkyl Heck-couplings of vinylarenes with umpolung aldehydes catalyzed by nickel
inferred← citeshttps://doi.org/10.1038/s41467-021-21270-9openalex-snapshot
Pd-catalyzed formal Mizoroki–Heck coupling of unactivated alkyl chlorides
inferred← citeshttps://doi.org/10.1038/s41467-021-24596-6openalex-snapshot
Organozinc pivalates for cobalt-catalyzed difluoroalkylarylation of alkenes
inferred← citeshttps://doi.org/10.1038/s41929-025-01438-yopenalex-snapshot
Bismuth-photocatalysed Heck-type coupling with alkyl and aryl electrophiles
inferred← citeshttps://doi.org/10.1039/9781839169052-00689openalex-snapshot
Innovative Reactions Mediated by Zirconocene: Advantages and Scope*
inferred← citeshttps://doi.org/10.1039/b211499mopenalex-snapshot
19 Catalysis and organometallic chemistry of monometallic species
inferred← citeshttps://doi.org/10.1039/b311797aopenalex-snapshot
20 Catalysis and organometallic chemistry of monometallic species
inferred← citeshttps://doi.org/10.1039/b502134kopenalex-snapshot
One-pot β-substitution of enones with alkyl groups to β-alkyl enones
inferred← citeshttps://doi.org/10.1039/b507133jopenalex-snapshot
Simple iron-amine catalysts for the cross-coupling of aryl Grignards with alkyl halides bearing β-hydrogens
inferred← citeshttps://doi.org/10.1039/b601014hopenalex-snapshot
Iron nanoparticles in the coupling of alkyl halides with aryl Grignard reagents
inferred← citeshttps://doi.org/10.1039/b617556bopenalex-snapshot
A novel Heck reaction catalyzed by Co hollow nanospheres in ligand-free condition
inferred← citeshttps://doi.org/10.1039/b809626kopenalex-snapshot
Synthesis of functionalised diarylmethanes via a cobalt-catalysed cross-coupling of arylzinc species with benzyl chlorides
inferred← citeshttps://doi.org/10.1039/b813596gopenalex-snapshot
Titanocene-catalyzed alkylative dimerization of vinyl Grignard reagent using alkyl halides
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