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Kumada Coupling of Aryl and Vinyl Tosylates under Mild Conditions
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-3773(20020215)41:4<609::aid-anie609>3.0.co;2-mopenalex-snapshot
Iron-Catalyzed Cross-Coupling Reactions of Alkyl-Grignard Reagents with Aryl Chlorides, Tosylates, and Triflates
inferredcites →https://doi.org/10.1002/1521-3773(20021104)41:21<4056::aid-anie4056>3.0.co;2-8openalex-snapshot
Palladium-Catalyzed Coupling of Alkyl Chlorides and Grignard Reagents
inferredcites →https://doi.org/10.1002/1521-3773(20021115)41:22<4176::aid-anie4176>3.0.co;2-uopenalex-snapshot
Palladium-Catalyzed Coupling Reactions of Aryl Chlorides
inferredcites →https://doi.org/10.1002/9783527612222openalex-snapshot
Metal‐Catalyzed Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/9783527619535openalex-snapshot
Metal‐Catalyzed Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/anie.198605081openalex-snapshot
The Palladium‐Catalyzed Cross‐Coupling Reactions of Organotin Reagents with Organic Electrophiles [New Synthetic Methods (58)]
inferredcites →https://doi.org/10.1002/chin.200345079openalex-snapshot
Oxidative Addition of Aryl Tosylates to Palladium(0) and Coupling of Unactivated Aryl Tosylates at Room Temperature.
inferredcites →https://doi.org/10.1016/0040-4039(96)01984-3openalex-snapshot
Nickel-catalyzed coupling reaction of lithium organoborates and aryl mesylates possessing an electron withdrawing group
inferredcites →https://doi.org/10.1016/s0022-328x(98)01055-9openalex-snapshot
Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998
inferredcites →https://doi.org/10.1016/s0040-4020(02)00411-8openalex-snapshot
Syntheses of substituted pyridines, quinolines and diazines via palladium-catalyzed cross-coupling of aryl Grignard reagents
inferredcites →https://doi.org/10.1016/s0040-4039(98)01928-5openalex-snapshot
A new method for the preparation of alkynes from vinyl triflates
inferredcites →https://doi.org/10.1016/s1381-1169(01)00153-4openalex-snapshot
Palladium metal catalysts in Heck CC coupling reactions
inferredcites →https://doi.org/10.1021/cr00039a007openalex-snapshot
Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
inferredcites →https://doi.org/10.1021/cr9903048openalex-snapshot
The Heck Reaction as a Sharpening Stone of Palladium Catalysis
inferredcites →https://doi.org/10.1021/ja00088a047openalex-snapshot
A Novel Easily Accessible Chiral Ferrocenyldiphosphine for Highly Enantioselective Hydrogenation, Allylic Alkylation, and Hydroboration Reactions
inferredcites →https://doi.org/10.1021/ja00313a032openalex-snapshot
Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II): an effective catalyst for cross-coupling of secondary and primary alkyl Grignard and alkylzinc reagents with organic halides
inferredcites →https://doi.org/10.1021/ja00767a075openalex-snapshot
Selective carbon-carbon bond formation by cross-coupling of Grignard reagents with organic halides. Catalysis by nickel-phosphine complexes
inferredcites →https://doi.org/10.1021/ja027190topenalex-snapshot
Iron-Catalyzed Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/ja035483wopenalex-snapshot
Expanding Pd-Catalyzed C−N Bond-Forming Processes: The First Amidation of Aryl Sulfonates, Aqueous Amination, and Complementarity with Cu-Catalyzed Reactions
inferredcites →https://doi.org/10.1021/ja035835zopenalex-snapshot
Oxidative Addition of Aryl Tosylates to Palladium(0) and Coupling of Unactivated Aryl Tosylates at Room Temperature
inferredcites →https://doi.org/10.1021/ja0363258openalex-snapshot
Palladium-Catalyzed Negishi Cross-Coupling Reactions of Unactivated Alkyl Iodides, Bromides, Chlorides, and Tosylates
inferredcites →https://doi.org/10.1021/ja036947topenalex-snapshot
The First General Palladium Catalyst for the Suzuki−Miyaura and Carbonyl Enolate Coupling of Aryl Arenesulfonates
inferredcites →https://doi.org/10.1021/ja038752ropenalex-snapshot
Room-Temperature Ni(0)-Catalyzed Cross-Coupling Reactions of Aryl Arenesulfonates with Arylboronic Acids
inferredcites →https://doi.org/10.1021/ja0389366openalex-snapshot
Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides
inferredcites →https://doi.org/10.1021/ja049744topenalex-snapshot
Iron-Catalyzed Cross-Coupling of Primary and Secondary Alkyl Halides with Aryl Grignard Reagents
inferredcites →https://doi.org/10.1021/ja981318iopenalex-snapshot
Sterically Hindered Chelating Alkyl Phosphines Provide Large Rate Accelerations in Palladium-Catalyzed Amination of Aryl Iodides, Bromides, and Chlorides, and the First Amination of Aryl Tosylates
inferredcites →https://doi.org/10.1021/ja983378uopenalex-snapshot
Simple, Highly Active Palladium Catalysts for Ketone and Malonate Arylation: Dissecting the Importance of Chelation and Steric Hindrance
inferredcites →https://doi.org/10.1021/ja991703nopenalex-snapshot
Efficient Cross-Coupling of Aryl Chlorides with Aryl Grignard Reagents (Kumada Reaction) Mediated by a Palladium/Imidazolium Chloride System
inferredcites →https://doi.org/10.1021/jo0005518openalex-snapshot
Stereochemistry in the Reaction of 4-Methyl-1,2,4-triazoline-3,5-dione (MTAD) with β,β-Dimethyl-p-methoxystyrene. Are Open Biradicals the Reaction Intermediates?
inferredcites →https://doi.org/10.1021/jo00126a047openalex-snapshot
Aryl Mesylates in Metal Catalyzed Homo- and Cross-Coupling Reactions. 4. Scope and Limitations of Aryl Mesylates in Nickel Catalyzed Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/jo00281a036openalex-snapshot
Comparative substituent effects of tosyloxy, benzoyloxy, and phosphoryloxy substituents in carbocation formation. Acid-catalyzed hydration of vinyl tosylates, benzoates, and 1,1-ditosylates
inferredcites →https://doi.org/10.1021/jo00979a024openalex-snapshot
Palladium-catalyzed vinylic hydrogen substitution reactions with aryl, benzyl, and styryl halides
inferredcites →https://doi.org/10.1021/jo026449nopenalex-snapshot
Nickel(0)-Catalyzed Cross-Coupling of Alkyl Arenesulfonates with Aryl Grignard Reagents
inferredcites →https://doi.org/10.1021/jo049940iopenalex-snapshot
NiCl2(dppe)-Catalyzed Cross-Coupling of Aryl Mesylates, Arenesulfonates, and Halides with Arylboronic Acids
inferredcites →https://doi.org/10.1021/jo981191fopenalex-snapshot
Dichloro[(2-dimethylamino)propyldiphenylphosphine]palladium(II) (PdCl2(alaphos)): An Efficient Catalyst for Cross-Coupling of Aryl Triflates with Alkynyl Grignard Reagents1
inferredcites →https://doi.org/10.1021/ol016526lopenalex-snapshot
NiCl2(PCy3)2: A Simple and Efficient Catalyst Precursor for the Suzuki Cross-Coupling of Aryl Tosylates and Arylboronic Acids
inferredcites →https://doi.org/10.1021/ol049686gopenalex-snapshot
Kumada−Corriu Reactions of Alkyl Halides with Alkynyl Nucleophiles
inferredcites →https://doi.org/10.1021/ol049779yopenalex-snapshot
Iron-Catalyzed Grignard Cross-Coupling with Alkyl Halides Possessing β-Hydrogens
inferredcites →https://doi.org/10.1021/ol050117yopenalex-snapshot
Preparation of Enamides via Palladium-Catalyzed Amidation of Enol Tosylates
inferredcites →https://doi.org/10.1039/b300033hopenalex-snapshot
Kumada–Corriu coupling of Grignard reagents, probed with a chiral Grignard reagent
inferredcites →https://doi.org/10.1039/c39930001682openalex-snapshot
ortho-Substituted unsymmetrical biaryls from aryl tert-butyl sulfones
inferredcites →https://doi.org/10.1055/s-1998-1616openalex-snapshot
Palladium-Catalyzed Alkoxycarbonylation of Aryl p-Toluenesulfonate
inferredcites →https://doi.org/10.1055/s-2000-6287openalex-snapshot
Catalytic Coupling of Aryl Sulfonates with sp2-Hybridized Nitrogen Nucleophiles: Palladium- and Nickel-catalyzed Synthesis of N-Aryl Sulfoximines
inferredcites →https://doi.org/10.1055/s-2001-18748openalex-snapshot
Fe(III)-Catalyzed Cross-Coupling Between Functionalized Arylmagnesium Compounds and Alkenyl Halides
inferredcites →https://doi.org/10.1080/00945710009351811openalex-snapshot
Copper Catalyzed Reactions of Aryl Grignard Reagents with Aryl Arenesulfonates
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Josiphos Ligands, (R,SFc)- and (S,RFc)-1-(Phosphino)-2-(1-phosphino ethyl)-ferrocene
inferred← citeshttps://doi.org/10.1002/047084289x.rn00874.pub2openalex-snapshot
R)-1-[(1R)-1-(Dicyclohexylphosphino) ethyl]-2-(diphenylphosphino)-ferrocene and (2S)-1-[(1R)-1-(Dicyclohexylphosphino) ethyl]-2-(diphenylphosphino)-ferrocene (Josiphos)
inferred← citeshttps://doi.org/10.1002/9781118662083.cot01-002openalex-snapshot
Formation of Alkanes and Arenes by Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9781118662083.cot02-005openalex-snapshot
Formation of Alkenes by Metal‐promoted Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9781118788981.ch5openalex-snapshot
Homogeneous Transition‐Metal‐Catalyzed C–O Bond Activation
inferred← citeshttps://doi.org/10.1002/9783527603978.mst0417openalex-snapshot
The Synthesis of Conjugated Polythiophenes by K umada Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/9783527623273.ch5openalex-snapshot
Iron‐Catalyzed Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9783527627325.ch2openalex-snapshot
Metal‐Catalyzed Coupling Reactions with Aryl Chlorides, Tosylates and Fluorides
inferred← citeshttps://doi.org/10.1002/9783527628841.ch4openalex-snapshot
Bidentate 1,2‐Ferrocenyl Diphosphine Ligands
inferred← citeshttps://doi.org/10.1002/9783527635207.ch3openalex-snapshot
Josiphos Ligands: From Discovery to Technical Applications
inferred← citeshttps://doi.org/10.1002/9783527655588.ch5openalex-snapshot
Carbon–Carbon‐Bond‐Forming Reactions Mediated by Organomagnesium Reagents
inferred← citeshttps://doi.org/10.1002/adsc.201100151openalex-snapshot
Room Temperature Nickel(II) Complexes [(4‐MeOC6H4)Ni(PCy3)2OTs and Ni(PCy3)2X2]‐Catalyzed Cross‐Coupling Reactions of Aryl/Alkenyl Sulfonates with Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/adsc.201200447openalex-snapshot
Thioethers as Directing Group for the Palladium‐Catalyzed Direct Arylation of Arenes
inferred← citeshttps://doi.org/10.1002/adsc.201801586openalex-snapshot
Nickel‐Catalyzed C(sp2)−C(sp3) Kumada Cross‐Coupling of Aryl Tosylates with Alkyl Grignard Reagents
inferred← citeshttps://doi.org/10.1002/adsc.70757openalex-snapshot
Unlocking the Potential of Organoaluminum Reagents for Versatile C─C Couplings Using YPhos‐Pd Catalysts
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Iron‐Catalyzed Kumada Cross‐Coupling Reactions of Pyrimidin‐2‐yl Phosphates: An Efficient Approach to C2‐Functionalized Pyrimidines
inferred← citeshttps://doi.org/10.1002/ajoc.202100031openalex-snapshot
Palladium‐Phenylpyrazolylphosphine‐Catalyzed Cross‐Coupling of Alkenyl Pivalates
inferred← citeshttps://doi.org/10.1002/ajoc.202500332openalex-snapshot
Advanced Pd–NAPA Precatalysts for Broad‐Scope Kumada–Tamao–Corriu Couplings of Challenging Aryl Chlorides
inferred← citeshttps://doi.org/10.1002/ange.200504450openalex-snapshot
Katalytische Arylierungen über C‐H‐Bindungsaktivierung mit Aryltosylaten
inferred← citeshttps://doi.org/10.1002/ange.200600442openalex-snapshot
Heck Coupling with Nonactivated Alkenyl Tosylates and Phosphates: Examples of Effective 1,2‐Migrations of the Alkenyl Palladium(II) Intermediates
inferred← citeshttps://doi.org/10.1002/ange.200601872openalex-snapshot
Kaskadenreaktionen in der Totalsynthese
inferred← citeshttps://doi.org/10.1002/ange.200705558openalex-snapshot
Palladium‐Catalyzed Intermolecular Ene–Yne Coupling: Development of an Atom‐Efficient Mizoroki–Heck‐Type Reaction
inferred← citeshttps://doi.org/10.1002/ange.200802157openalex-snapshot
Palladium‐Catalyzed Amination of Aryl Mesylates
inferred← citeshttps://doi.org/10.1002/ange.200803193openalex-snapshot
A General Palladium‐Catalyzed Suzuki–Miyaura Coupling of Aryl Mesylates
inferred← citeshttps://doi.org/10.1002/ange.200803730openalex-snapshot
Radikalkatalyse in der Kumada‐Kreuzkupplung mit funktionalisierten Grignard‐Reagentien
inferred← citeshttps://doi.org/10.1002/ange.200904033openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling of Aryl Halides Using Organotitanium Nucleophiles
inferred← citeshttps://doi.org/10.1002/ange.200905953openalex-snapshot
Decarboxylative Cross‐Coupling of Aryl Tosylates with Aromatic Carboxylate Salts
inferred← citeshttps://doi.org/10.1002/ange.201002745openalex-snapshot
Selective cine Substitution of 1‐Arylethenyl Acetates with Arylboron Reagents and a Diene/Rhodium Catalyst
inferred← citeshttps://doi.org/10.1002/ange.201609635openalex-snapshot
Rapid Room‐Temperature, Chemoselective C−C Coupling of Poly(pseudo)halogenated Arenes Enabled by Palladium(I) Catalysis in Air
inferred← citeshttps://doi.org/10.1002/ange.202005286openalex-snapshot
Direct Umpolung Morita–Baylis–Hillman like α‐Functionalization of Enones via Enolonium Species
inferred← citeshttps://doi.org/10.1002/ange.202008866openalex-snapshot
Efficient Pd‐Catalyzed Direct Coupling of Aryl Chlorides with Alkyllithium Reagents
inferred← citeshttps://doi.org/10.1002/ange.202212522openalex-snapshot
Rhodium‐Catalyzed Divergent Arylation of Alkenylsulfonium Salts with Arylboroxines
inferred← citeshttps://doi.org/10.1002/anie.200504450openalex-snapshot
Catalytic Arylation Reactions by CH Bond Activation with Aryl Tosylates
inferred← citeshttps://doi.org/10.1002/anie.200600442openalex-snapshot
Heck Coupling with Nonactivated Alkenyl Tosylates and Phosphates: Examples of Effective 1,2‐Migrations of the Alkenyl Palladium(II) Intermediates
inferred← citeshttps://doi.org/10.1002/anie.200601872openalex-snapshot
Cascade Reactions in Total Synthesis
inferred← citeshttps://doi.org/10.1002/anie.200705558openalex-snapshot
Palladium‐Catalyzed Intermolecular Ene–Yne Coupling: Development of an Atom‐Efficient Mizoroki–Heck‐Type Reaction
inferred← citeshttps://doi.org/10.1002/anie.200802157openalex-snapshot
Palladium‐Catalyzed Amination of Aryl Mesylates
inferred← citeshttps://doi.org/10.1002/anie.200803193openalex-snapshot
A General Palladium‐Catalyzed Suzuki–Miyaura Coupling of Aryl Mesylates
inferred← citeshttps://doi.org/10.1002/anie.200803730openalex-snapshot
Radical Catalysis of Kumada Cross‐Coupling Reactions Using Functionalized Grignard Reagents
inferred← citeshttps://doi.org/10.1002/anie.200904033openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling of Aryl Halides Using Organotitanium Nucleophiles
inferred← citeshttps://doi.org/10.1002/anie.200905953openalex-snapshot
Decarboxylative Cross‐Coupling of Aryl Tosylates with Aromatic Carboxylate Salts
inferred← citeshttps://doi.org/10.1002/anie.201002745openalex-snapshot
Selective cine Substitution of 1‐Arylethenyl Acetates with Arylboron Reagents and a Diene/Rhodium Catalyst
inferred← citeshttps://doi.org/10.1002/anie.201609635openalex-snapshot
Rapid Room‐Temperature, Chemoselective C−C Coupling of Poly(pseudo)halogenated Arenes Enabled by Palladium(I) Catalysis in Air
inferred← citeshttps://doi.org/10.1002/anie.202005286openalex-snapshot
Direct Umpolung Morita–Baylis–Hillman like α‐Functionalization of Enones via Enolonium Species
inferred← citeshttps://doi.org/10.1002/anie.202008866openalex-snapshot
Efficient Pd‐Catalyzed Direct Coupling of Aryl Chlorides with Alkyllithium Reagents
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Rhodium‐Catalyzed Divergent Arylation of Alkenylsulfonium Salts with Arylboroxines
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Unconventional β ‐Hydride Elimination in Pd‐Catalyzed Migratory Cyclization: A Theoretical Study of Outer‐Sphere C(sp 2 )–H Activation
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Addition of Sulfonic Acids to Terminal Alkynes Catalyzed by a Rhodium Complex: Ligand Concentration‐Controlled Reaction Selectivity
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Experimental and DFT Study of the Tautomeric Behavior of Cobalt‐Containing Secondary Phosphine Oxides
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Classical Reagents: New Surprises in Palladium‐Catalyzed CC Coupling Reactions
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Pd‐Catalyzed CN Bond Formation with Heteroaromatic Tosylates
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Nickel‐Catalyzed Cross‐Coupling of Non‐Activated or Functionalized Aryl Halides with Aryl Grignard Reagents
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Activation of “Inert” Alkenyl/Aryl CO Bond and Its Application in Cross‐Coupling Reactions
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Palladium‐Catalyzed Direct Arylation of Heteroarenes with Aryl Mesylates
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Well‐Defined Air‐Stable Palladium HASPO Complexes for Efficient Kumada–Corriu Cross‐Couplings of (Hetero)Aryl or Alkenyl Tosylates
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Gold(I)‐Catalyzed Stereoselective Synthesis of Alkenyl Phosphates by Hydrophosphoryloxylation
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Pd‐Catalyzed Difluoromethylation of Vinyl Bromides, Triflates, Tosylates, and Nonaflates
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Unconventional Reactivity of (Z)‐Enoate Propargylic Alcohols in the Presence of Acids
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Chemodivergence between Electrophiles in Cross‐Coupling Reactions
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Stereoselective Synthesis of Tetraarylethylenes Enabled by Reductive anti‐ 1,2‐Dimetallation of Alkynes
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Kumada Coupling of Aryl and Vinyl Tosylates under Mild Conditions.
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ChemInform Abstract: Practical Aspects of Carbon—Carbon Cross‐Coupling Reactions Using Heteroarenes
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Nickel‐Catalyzed Cross‐Coupling with Pincer Ligands
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N‐Heterocyclic Carbene Derived Nickel–Pincer Complexes: Efficient and Applicable Catalysts for Suzuki–Miyaura Coupling Reactions of Aryl/Alkenyl Tosylates and Mesylates
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Efficient Synthesis of Biaryls through the Kumada Reaction Catalyzed by Carbene Adducts of Cyclopalladated Ferrocenylimine
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Diels–Alder Reactions for the Construction of Cyclopropylarenes
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Rose‐Bengal‐Photocatalyzed Cross‐Dehydrogenative Coupling Reactions under Visible Light
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2‐Pyridyl Tosylate Derivatives—Building Blocks for Structural Diversity via Transition Metal Catalysis
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Air‐Stable Bifunctional HASPO Preligands for Metal‐Catalyzed Cross‐Couplings and Direct C–H Bond Arylations
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Nickel‐catalyzed Kumada Cross‐coupling Reaction for the Synthesis of 2,4‐Diarylquinazolines
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An overview of palladium‐catalyzed synthesis of seven‐membered heterocycles
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Stereocomplementary and Parallel Syntheses of Multi‐Substituted (E)‐, (Z)‐Stereodefined α,β‐Unsaturated Esters: Application to Drug Syntheses
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Chelation-Assisted Arylation via C–H Bond Cleavage
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Pd(NHC)(cinnamyl)Cl-catalyzed Suzuki cross-coupling reaction of aryl sulfonates with arylboronic acids
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3.04 Alkylations of Nonstabilized Carbanions
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Cross-Coupling Reactions
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Chiral Phosphorous Ligands in Asymmetric Catalysis
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Coupling Reactions Between sp3 and sp2 Carbon Centers
inferred← citeshttps://doi.org/10.1016/j.catcom.2024.106862openalex-snapshot
Magnetically retractable tea extract stabilized palladium nanoparticles for denitrogenative cross-coupling of aryl bromides with arylhydrazines under green conditions: An alternate route for the biaryls synthesis
inferred← citeshttps://doi.org/10.1016/j.ccr.2007.03.011openalex-snapshot
Transition metals in organic synthesis: Highlights for the year 2005
inferred← citeshttps://doi.org/10.1016/j.comptc.2018.03.025openalex-snapshot
Theoretical insights on the C-C bond reductive elimination from Co(III) center
inferred← citeshttps://doi.org/10.1016/j.jcat.2018.06.012openalex-snapshot
Structural elucidation of supported Rh complexes derived from RhCl(PPh3)3 immobilized on surface-functionalized SBA-15 and their catalytic performance for C-heteroatom (S, O) bond formation
inferred← citeshttps://doi.org/10.1016/j.jcat.2023.08.006openalex-snapshot
One metal two tasks: Reentering the catalytic ending PdII-H for the relay-catalytic cycle for dicarbonylation of amines
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.02.039openalex-snapshot
Electrochemistry and complexation of Josiphos ligands
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.07.035openalex-snapshot
Highly efficient gold(III)-catalyzed intermolecular hydroarylation of unactivated alkenes with arenes under mild conditions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.10.005openalex-snapshot
Amination and Suzuki coupling reactions catalyzed by palladium complexes coordinated by cobalt-containing monodentate phosphine ligands with bis-trifluoromethyl substituents on bridged arylethynyl: Observation of some unusual metal-containing compounds
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.12.046openalex-snapshot
Preparation of a cobalt-containing P,N-bidentate ligand ligated palladium complex: Its applications in amination and Suzuki cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2023.122737openalex-snapshot
Graphene loaded with metal nanoparticles/complexes catalyzed cross-coupling reactions: A review
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2024.123444openalex-snapshot
Recent advances on Pd schiff base catalysts in suzuki-miyaura cross-coupling reaction: A review
inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.128635openalex-snapshot
Regio-isomeric isoxazole sulfonates: Synthesis, characterization, electrochemical studies and DNA binding activity
inferred← citeshttps://doi.org/10.1016/j.tet.2007.08.017openalex-snapshot
Heterogeneous Pd/C-catalyzed ligand-free Suzuki–Miyaura coupling reaction using aryl boronic esters
inferred← citeshttps://doi.org/10.1016/j.tet.2007.10.091openalex-snapshot
Naphthidine di(radical cation)s-stabilized palladium nanoparticles for efficient catalytic Suzuki–Miyaura cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2007.12.039openalex-snapshot
Reaction of secondary and tertiary aliphatic halides with aromatic aldehydes mediated by chromium(II): a selective cross-coupling of alkyl and ketyl radicals
inferred← citeshttps://doi.org/10.1016/j.tet.2008.01.020openalex-snapshot
Pd(OAc)2-catalyzed domino reactions of 1,2-dihaloarenes and 2-haloaryl arenesulfonates with Grignard reagents: efficient synthesis of substituted fluorenes
inferred← citeshttps://doi.org/10.1016/j.tet.2008.01.050openalex-snapshot
[RuCl3(H2O)n]-catalyzed direct arylations
inferred← citeshttps://doi.org/10.1016/j.tet.2008.04.011openalex-snapshot
A new palladium catalyzed protocol for atom-efficient cross-coupling reactions of triarylbismuths with aryl halides and triflates
inferred← citeshttps://doi.org/10.1016/j.tet.2009.04.057openalex-snapshot
The effect of ortho-substitution on the efficacy of biphenyls in mediating electron transfer from lithium
inferred← citeshttps://doi.org/10.1016/j.tet.2013.09.039openalex-snapshot
Iron-catalyzed cross-coupling of aryltrimethylammonium triflates and alkyl Grignard reagents
inferred← citeshttps://doi.org/10.1016/j.tet.2015.06.103openalex-snapshot
Recyclable palladium catalyst on grapheme oxide for the C–C/C–N cross-coupling reactions of heteroaromatic sulfonates
inferred← citeshttps://doi.org/10.1016/j.tet.2015.10.069openalex-snapshot
Newly-generated Al(OH) 3 -supported Pd nanoparticles-catalyzed Stille and Kumada coupling reactions of diazonium salts, (Het)aryl chlorides
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.07.032openalex-snapshot
Iridium-catalyzed asymmetric hydrogenation of olefins using TIQ phosphine–oxazoline ligands
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.06.012openalex-snapshot
Preparation and decarboxylative rearrangement of (Z)-enyne esters
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.05.054openalex-snapshot
General and user-friendly protocol for the synthesis of functionalized aryl- and heteroaryl-cyclopropanes by Negishi cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.10.096openalex-snapshot
An efficient route to 4-substituted coumarins, 2(5H)-furanones, and pyrones via palladium-catalyzed couplings of alkenyl tosylates with organoindium reagents
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.10.163openalex-snapshot
A new one-pot solvent-free synthesis of pyridinyl tosylates via diazotization of aminopyridines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.06.041openalex-snapshot
A novel method for tosyloxylation of anilides using phenyliodine bistrifluoroacetate (PIFA)
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.12.022openalex-snapshot
Acid-promoted cyclization of 2-propynolphenols leading to 4-tosyloxy-2H-chromenes
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.7b01707openalex-snapshot
Triazolylidene Iridium Complexes for Highly Efficient and Versatile Transfer Hydrogenation of C═O, C═N, and C═C Bonds and for Acceptorless Alcohol Oxidation
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01458openalex-snapshot
Synthesis of β,β-Disubstituted Styrenes via Trimethylsilyl Trifluoromethanesulfonate-Promoted Aldehyde-Aldehyde Aldol Coupling-Elimination
inferred← citeshttps://doi.org/10.1021/acs.organomet.0c00775openalex-snapshot
16-Electron Nickel(0)-Olefin Complexes in Low-Temperature C(sp2)–C(sp3) Kumada Cross-Couplings
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03961openalex-snapshot
N-Pyridylimidates as Traceless Acyl Equivalents for Directed C–O Bond Functionalization
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02185openalex-snapshot
Ni-Catalyzed Kumada–Corriu Cross-Coupling Reactions of Tertiary Grignard Reagents and Bromostyrenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00562openalex-snapshot
Electrochemical Synthesis of Vinyl Sulfonates Mediated by Bromine Radicals
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00496openalex-snapshot
Catalyst-Free and Solvent-Controlled Reductive Coupling of Activated Vinyl Triflates with Chlorotrimethylsilane by Magnesium Metal and Its Synthetic Application
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00854openalex-snapshot
General Synthesis of Alkenyl Sulfides by Palladium-Catalyzed Thioetherification of Alkenyl Halides and Tosylates
inferred← citeshttps://doi.org/10.1021/acscatal.2c00352openalex-snapshot
Tunable Unsymmetrical Ferrocene Ligands Bearing a Bulky Di-1-adamantylphosphino Motif for Many Kinds of Csp2–Csp3 Couplings
inferred← citeshttps://doi.org/10.1021/acscatal.5c07930openalex-snapshot
Mechanistically Driven Development of Kumada Catalyst-Transfer Polymerizations: A Rapid Injection NMR Study
inferred← citeshttps://doi.org/10.1021/acscatal.6c01027openalex-snapshot
Recent Advances in Transition-Metal-Catalyzed Cine -Coupling Reactions
inferred← citeshttps://doi.org/10.1021/cc0600066openalex-snapshot
Revisiting Benzenesulfonyl Linker for the Deoxygenation and Multifunctionalization of Phenols
inferred← citeshttps://doi.org/10.1021/cr100327popenalex-snapshot
Advances in Transition Metal (Pd,Ni,Fe)-Catalyzed Cross-Coupling Reactions Using Alkyl-organometallics as Reaction Partners
inferred← citeshttps://doi.org/10.1021/cr9000786openalex-snapshot
Cobalt-Catalyzed Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/ja070321bopenalex-snapshot
Studies on the Heck Reaction with Alkenyl Phosphates: Can the 1,2-Migration Be Controlled? Scope and Limitations
inferred← citeshttps://doi.org/10.1021/ja105096ropenalex-snapshot
Switch of Regioselectivity in Palladium-Catalyzed Silaboration of Terminal Alkynes by Ligand-Dependent Control of Reductive Elimination
inferred← citeshttps://doi.org/10.1021/ja200398copenalex-snapshot
Suzuki−Miyaura Cross-Coupling of Aryl Carbamates and Sulfamates: Experimental and Computational Studies
inferred← citeshttps://doi.org/10.1021/ja804672mopenalex-snapshot
Palladium-Catalyzed Hiyama Cross-Couplings of Aryl Arenesulfonates with Arylsilanes
inferred← citeshttps://doi.org/10.1021/ja805810popenalex-snapshot
Palladium-Catalyzed Amination of Aryl and Heteroaryl Tosylates at Room Temperature
inferred← citeshttps://doi.org/10.1021/ja903091gopenalex-snapshot
Hydroxyphosphine Ligand for Nickel-Catalyzed Cross-Coupling through Nickel/Magnesium Bimetallic Cooperation
inferred← citeshttps://doi.org/10.1021/ja904152ropenalex-snapshot
Iridium Phosphite−Oxazoline Catalysts for the Highly Enantioselective Hydrogenation of Terminal Alkenes
inferred← citeshttps://doi.org/10.1021/jacs.0c06995openalex-snapshot
Small Phosphine Ligands Enable Selective Oxidative Addition of Ar–O over Ar–Cl Bonds at Nickel(0)
inferred← citeshttps://doi.org/10.1021/jacs.2c08765openalex-snapshot
Isolation and Characterization of Heteroleptic Mononuclear Palladium(I) Complexes
inferred← citeshttps://doi.org/10.1021/jacs.8b09849openalex-snapshot
A Highly Reduced Ni–Li–Olefin Complex for Catalytic Kumada–Corriu Cross-Couplings
inferred← citeshttps://doi.org/10.1021/jo070912kopenalex-snapshot
Investigations on the Suzuki−Miyaura and Negishi Couplings with Alkenyl Phosphates: Application to the Synthesis of 1,1-Disubstituted Alkenes
inferred← citeshttps://doi.org/10.1021/jo100983copenalex-snapshot
Palladium-Catalyzed Cross-Coupling of Cyclopropylmagnesium Bromide with Aryl Bromides Mediated by Zinc Halide Additives
inferred← citeshttps://doi.org/10.1021/jo300290vopenalex-snapshot
Probing for a Leaving Group Effect on the Generation and Reactivity of Phenyl Cations
inferred← citeshttps://doi.org/10.1021/jo301270topenalex-snapshot
N-Heterocyclic Carbene–Palladium(II)–1-Methylimidazole Complex-Catalyzed Suzuki–Miyaura Coupling of Aryl Sulfonates with Arylboronic Acids
inferred← citeshttps://doi.org/10.1021/jo502172copenalex-snapshot
Aryl Imidazylates and Aryl Sulfates As Electrophiles in Metal-Free ArSN1 Reactions
inferred← citeshttps://doi.org/10.1021/jo701893mopenalex-snapshot
Efficient Synthesis of Sterically Crowded Biaryls by Palladium-Phosphinous Acid-Catalyzed Cross-Coupling of Aryl Halides and Aryl Grignards
inferred← citeshttps://doi.org/10.1021/jo702377hopenalex-snapshot
Palladium-Catalyzed Cross-Coupling Reaction of Tricyclopropylbismuth with Aryl Halides and Triflates
inferred← citeshttps://doi.org/10.1021/jo7027097openalex-snapshot
Direct Vinylation and Difluorovinylation of Arylboronic Acids Using Vinyl- and 2,2-Difluorovinyl Tosylates via the Suzuki−Miyaura Cross Coupling
inferred← citeshttps://doi.org/10.1021/jo8014819openalex-snapshot
Suzuki−Miyaura Coupling of Aryl Tosylates Catalyzed by an Array of Indolyl Phosphine−Palladium Catalysts
inferred← citeshttps://doi.org/10.1021/jo801824eopenalex-snapshot
Studies on the 1,2-Migrations in Pd-Catalyzed Negishi Couplings with JosiPhos Ligands
inferred← citeshttps://doi.org/10.1021/jo900098aopenalex-snapshot
A Ligand Free and Room Temperature Protocol for Pd-Catalyzed Kumada−Corriu Couplings of Unactivated Alkenyl Phosphates
inferred← citeshttps://doi.org/10.1021/ol061116oopenalex-snapshot
Air-Stable PinP(O)H as Preligand for Palladium-Catalyzed Kumada Couplings of Unactivated Tosylates
inferred← citeshttps://doi.org/10.1021/ol061989iopenalex-snapshot
Pd(OAc)2-Catalyzed Domino Reactions of 1-Chloro-2-haloarenes and 2-Haloaryl Tosylates with Hindered Grignard Reagents via Palladium-Associated Arynes
inferred← citeshttps://doi.org/10.1021/ol102645gopenalex-snapshot
Monofluorovinyl Tosylate: A Useful Building Block for the Synthesis of Terminal Vinyl Monofluorides via Suzuki−Miyaura Coupling
inferred← citeshttps://doi.org/10.1021/ol1029996openalex-snapshot
Copper-Free Sonogashira Coupling of Cyclopropyl Iodides with Terminal Alkynes
inferred← citeshttps://doi.org/10.1021/ol2010165openalex-snapshot
Ligand Effects on Negishi Couplings of Alkenyl Halides
inferred← citeshttps://doi.org/10.1021/ol300908gopenalex-snapshot
K2CO3-Catalyzed Synthesis of Chromones and 4-Quinolones through the Cleavage of Aromatic C–O Bonds
inferred← citeshttps://doi.org/10.1021/ol401727yopenalex-snapshot
Nickel-Catalyzed Suzuki–Miyaura Couplings in Green Solvents
inferred← citeshttps://doi.org/10.1021/ol802049topenalex-snapshot
Palladium-Catalyzed Hiyama Cross-Coupling Reactions of Aryl Mesylates
inferred← citeshttps://doi.org/10.1021/ol802493zopenalex-snapshot
Palladium−Indolylphosphine-Catalyzed Hiyama Cross-Coupling of Aryl Mesylates
inferred← citeshttps://doi.org/10.1021/om800580popenalex-snapshot
Synthesis and Characterization of Amido Pincer Complexes of Lithium and Nickel and Catalysis of the Nickel Complexes in the Kumada Cross-Coupling
inferred← citeshttps://doi.org/10.1021/om900435yopenalex-snapshot
Application of Tautomerism of Ferrocenyl Secondary Phosphine Oxides in Suzuki−Miyaura Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/om9006399openalex-snapshot
N-Heterocyclic Carbene-Based Nickel Complexes: Synthesis and Catalysis in Cross-Couplings of Aryl Chlorides with ArMX (M = Mg or Zn)
inferred← citeshttps://doi.org/10.1021/om900771vopenalex-snapshot
Synthesis of Arylphosphonates via Palladium-Catalyzed Coupling Reactions of Aryl Imidazolylsulfonates with H-Phosphonate Diesters
inferred← citeshttps://doi.org/10.1021/op300236fopenalex-snapshot
Ni- and Fe-Catalyzed Cross-Coupling Reactions of Phenol Derivatives
inferred← citeshttps://doi.org/10.1021/op900221vopenalex-snapshot
Practical Aspects of Carbon−Carbon Cross-Coupling Reactions Using Heteroarenes
inferred← citeshttps://doi.org/10.1038/s41467-025-58633-5openalex-snapshot
Synthesis of benzoheterocycles by palladium-catalyzed migratory cyclization through an unexpected reaction cascade
inferred← citeshttps://doi.org/10.1039/b609064hopenalex-snapshot
Direct synthesis of 1,1-diarylalkenes from alkenyl phosphates via nickel(0)-catalysed Suzuki–Miyaura coupling
inferred← citeshttps://doi.org/10.1039/b818863gopenalex-snapshot
Gold-catalyzed addition of sulfonic acids to alkynes to form vinyl sulfonates
inferred← citeshttps://doi.org/10.1039/b924772fopenalex-snapshot
Retracted article: Cross coupling in water: Suzuki–Miyaura vinylation and difluorovinylation of arylboronic acids
inferred← citeshttps://doi.org/10.1039/c1cs15137aopenalex-snapshot
35 years of palladium-catalyzed cross-coupling with Grignard reagents: how far have we come?
inferred← citeshttps://doi.org/10.1039/c2cc33294aopenalex-snapshot
Ligand effects on the stereochemistry of Stille couplings, as manifested in reactions of Z-alkenyl halides
inferred← citeshttps://doi.org/10.1039/c3ra44884copenalex-snapshot
Kumada–Tamao–Corriu cross-coupling reaction of O-based electrophiles with Grignard reagents via C–O bond activation
inferred← citeshttps://doi.org/10.1039/c4cc05376aopenalex-snapshot
Cu-Catalyzed Suzuki–Miyaura reactions of primary and secondary benzyl halides with arylboronates
inferred← citeshttps://doi.org/10.1039/c4dt00250dopenalex-snapshot
The mechanism of catalytic methylation of 2-phenylpyridine using di-tert-butyl peroxide
inferred← citeshttps://doi.org/10.1039/c4ra09012hopenalex-snapshot
Pd-catalyzed cross-coupling reactions of less activated alkenyl electrophiles (for tosylates and mesylates) with tosylhydrazones: synthesis of various 1,3-dienes
inferred← citeshttps://doi.org/10.1039/c7cc06881fopenalex-snapshot
A simple route to 1,4-addition reactions by Co-catalyzed reductive coupling of organic tosylates and triflates with activated alkenes
inferred← citeshttps://doi.org/10.1039/c7cc08670aopenalex-snapshot
Practical synthesis of pharmaceutically relevant molecules enriched in sp 3 character
inferred← citeshttps://doi.org/10.1039/c7ob00578dopenalex-snapshot
[3,3]-Sigmatropic rearrangement of allenic alcohols: stereoselective synthesis of 1,3-diene-2-ol sulfonates
inferred← citeshttps://doi.org/10.1039/c9gc00617fopenalex-snapshot
Solvent effects in palladium catalysed cross-coupling reactions
inferred← citeshttps://doi.org/10.1039/d1nj03706dopenalex-snapshot
Synthesis of ortho -arylated and alkenylated benzamides by palladium-catalyzed denitrogenative cross-coupling reactions of 1,2,3-benzotriazin-4(3 H )-ones with organoboronic acids
inferred← citeshttps://doi.org/10.1055/a-1988-6052openalex-snapshot
Palladium-Catalyzed Denitrogenative Cross-Coupling of Silicon-Masked, Aryl-Substituted Diazenes and Aryl Bromides
inferred← citeshttps://doi.org/10.1080/00304940903507788openalex-snapshot
Arylcyclopropanes: Properties, Synthesis and Use in Medicinal Chemistry
inferred← citeshttps://doi.org/10.1080/00397911.2012.688160openalex-snapshot
RuCl3-Catalyzed Regioselective Diarylation with Aryl Tosylates via C-H Activation
inferred← citeshttps://doi.org/10.1080/00397911.2019.1582065openalex-snapshot
Transition metal- and oxidant-free sulfonylation of 1-sulfonyl-1H-1,2,3-triazoles to enols for the synthesis of sulfonate derivatives
inferred← citeshttps://doi.org/10.1080/17518253.2022.2107406openalex-snapshot
Mechanochemical Suzuki polymerization for the synthesis of polyfluorenes
inferred← citeshttps://doi.org/10.1107/s160053681001281xopenalex-snapshot
(E)-1,2-Diphenylethenyl methanesulfonate
inferred← citeshttps://doi.org/10.1134/s1070363222070246openalex-snapshot
Synthesis of Diarylmethanes via Pd-Catalyzed Coupling of Aryltosylates with Benzyltitanium Reagents
inferred← citeshttps://doi.org/10.1246/cl.2007.928openalex-snapshot
New Preparative Method of Aryl Tosylates by Using Organobismuth Reagents
inferred← citeshttps://doi.org/10.14233/ajchem.2025.33739openalex-snapshot
Kinetics, Pharmacokinetics, Drug-Likeness and Binding Affinity in Aqueous Iodinations of Regioisomers of Methyl Benzamine using Hydrodynamic Voltammetry, QSAR and Molecular Docking with Cytochrome P450
inferred← citeshttps://doi.org/10.1515/9783110352726-003openalex-snapshot
1. Grignard Reagents and Palladium
inferred← citeshttps://doi.org/10.1515/9783111739601-019openalex-snapshot
64718 Role of Kumada coupling reaction in organic synthesis
inferred← citeshttps://doi.org/10.1515/psr-2016-0018openalex-snapshot
Grignard Reagents and Palladium
inferred← citeshttps://doi.org/10.2174/2211544711666220629110020openalex-snapshot
Recent Advances in Palladium-catalyzed Borylation
inferred← citeshttps://doi.org/10.25135/acg.oc.94.20.12.1916openalex-snapshot
Carbon-carbon cross-coupling reactions of organomagnesium reagents with a variety of electrophilic substrates mediated by iron catalysts
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