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Hiyama Cross-Coupling of Arenediazonium Salts under Mild Reaction Conditions

https://doi.org/10.1021/jo201437j

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Density-functional thermochemistry. III. The role of exact exchange

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Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density

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Selective Synthesis of Unsymmetrical Biaryls via Palladium-Catalyzed Cross-Coupling of Arylfluorosilanes with Aryl Iodides

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.4847584openalex-extracted

Aryl/Hetero-Aryl Tosylates as Coupling Partners in Metal Mediated Suzuki and Hiyama Cross-Coupling Reactions in Ionic Liquids: Facile Synthesis of Biaryls/Heterobiaryls

inferred← citeshttps://doi.org/10.1002/9780471264194.fos07552.pub6openalex-snapshot

Palladium( II ) acetate

inferred← citeshttps://doi.org/10.1002/9780471264194.fos07552.pub7openalex-snapshot

Palladium( II ) acetate

inferred← citeshttps://doi.org/10.1002/9781118560273.ch6openalex-snapshot

Electrophilic Aromatic Substitution

inferred← citeshttps://doi.org/10.1002/9781118686263.ch4openalex-snapshot

Biaryls

inferred← citeshttps://doi.org/10.1002/9783527672707.ch1openalex-snapshot

Cross‐Coupling Arylations: Precedents and Rapid HistoricalReview of the Field

inferred← citeshttps://doi.org/10.1002/9783527814787.ch9openalex-snapshot

Transition‐Metal‐Catalyzed Cross‐coupling of Organosilicon Compounds

inferred← citeshttps://doi.org/10.1002/ajoc.201900295openalex-snapshot

Rhodium‐Catalyzed Hiyama Coupling Reaction of Unstrained Ketones via C−C Bond Cleavage

inferred← citeshttps://doi.org/10.1002/ange.201508161openalex-snapshot

Destruction and Construction: Application of Dearomatization Strategy in Aromatic Carbon–Nitrogen Bond Functionalization

inferred← citeshttps://doi.org/10.1002/ange.202014842openalex-snapshot

Base‐Free Cross‐Couplings of Aryl Diazonium Salts in Methanol: PdII–Alkoxy as Reactivity‐Controlling Intermediate

inferred← citeshttps://doi.org/10.1002/anie.201508161openalex-snapshot

Destruction and Construction: Application of Dearomatization Strategy in Aromatic Carbon–Nitrogen Bond Functionalization

inferred← citeshttps://doi.org/10.1002/anie.202014842openalex-snapshot

Base‐Free Cross‐Couplings of Aryl Diazonium Salts in Methanol: PdII–Alkoxy as Reactivity‐Controlling Intermediate

inferred← citeshttps://doi.org/10.1002/aoc.2932openalex-snapshot

Palladium nanoparticles supported on agarose‐catalyzed Heck–Matsuda and Suzuki–Miyaura coupling reactions using aryl diazonium salts

inferred← citeshttps://doi.org/10.1002/aoc.4203openalex-snapshot

Denitrogenative Pd/Cu‐catalyzed Suzuki‐type Cross‐coupling of Aryltrifluoroborates with Arylhydrazine Hydrochlorides in Water under Room Temperature

inferred← citeshttps://doi.org/10.1002/aoc.4484openalex-snapshot

Desulfinative and denitrogenative palladium‐catalyzed cross‐coupling of arylsulfonyl hydrazides with aryl diazonium salts

inferred← citeshttps://doi.org/10.1002/asia.201700174openalex-snapshot

Mechanistic Insights into Palladium‐Catalyzed Silylation of Aryl Iodides with Hydrosilanes through a DFT Study

inferred← citeshttps://doi.org/10.1002/chin.201212075openalex-snapshot

ChemInform Abstract: Hiyama Cross‐Coupling of Arenediazonium Salts under Mild Reaction Conditions.

inferred← citeshttps://doi.org/10.1002/ejic.201200622openalex-snapshot

Studies of the Electronic Properties of N‐Heterocyclic Carbene Ligands in the Context of Homogeneous Catalysis and Bioorganometallic Chemistry

inferred← citeshttps://doi.org/10.1002/ejoc.202001193openalex-snapshot

Recent Developments in Deaminative Functionalization of Alkyl Amines

inferred← citeshttps://doi.org/10.1002/ejoc.202201210openalex-snapshot

Aryltriazenes as Coupling Partners in the Hiyama, Hiyama‐Suzuki and Hiyama‐Heck Cross‐Coupling Reactions Using Conventional and Ionic Liquid Reagents and Solvents

inferred← citeshttps://doi.org/10.1002/slct.201701009openalex-snapshot

Straightforward and Recyclable System for Synthesis of Biaryl Ketones via Carbonylative Coupling Reactions of Aryl Halides with PhB(OH) 2 and (EtO) 3 PhSi

inferred← citeshttps://doi.org/10.1002/slct.202303273openalex-snapshot

Synthesis of Symmetrical Biaryls by Copper‐Catalysed Homocoupling of Aryltriazenes in Guanidinium Ionic Liquid

inferred← citeshttps://doi.org/10.1002/slct.202403925openalex-snapshot

Aryl/Hetero‐Aryl Tosylates as Coupling Partners in Metal‐Mediated Suzuki and Hiyama Cross‐Coupling Reactions in Ionic Liquids: Ligand‐Free Facile Synthesis of Biaryls/Heterobiaryls

inferred← citeshttps://doi.org/10.1002/tcr.201600063openalex-snapshot

The Hiyama Cross‐Coupling Reaction: New Discoveries

inferred← citeshttps://doi.org/10.1007/s11164-017-2888-5openalex-snapshot

In-situ-generated palladium nanoparticles in novel ionic liquid: an efficient catalytic system for Heck–Matsuda coupling

inferred← citeshttps://doi.org/10.1007/s11164-017-3102-5openalex-snapshot

Triton X-100 stabilized Pd nanoparticles and their catalytic application in one-pot sequential Heck and Hiyama coupling in water

inferred← citeshttps://doi.org/10.1007/s11696-021-02044-5openalex-snapshot

Palladium-catalyzed Hiyama cross-couplings of 2-chloro pyrimidines with organosilanes

inferred← citeshttps://doi.org/10.1016/j.tet.2014.08.035openalex-snapshot

Negishi cross-coupling of arenediazonium o-benzenedisulfonimides

inferred← citeshttps://doi.org/10.1016/j.tet.2017.06.004openalex-snapshot

Nickel-catalyzed cross-coupling of aryl or 2-menaphthyl quaternary ammonium triflates with organoaluminum reagents

inferred← citeshttps://doi.org/10.1016/j.tet.2019.130777openalex-snapshot

Pd-nanoparticles catalyzed denitrogenative coupling of aryl halides with arylhydrazines: Greener approach for biaryls synthesis under ligand-free condition

inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.09.001openalex-snapshot

Pd-catalyzed cross-coupling reactions of arenediazonium salts with arylsilanes and aryltrifluoroborates in water

inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.06.095openalex-snapshot

Palladium-catalyzed denitrogenative Hiyama cross-coupling with arylhydrazines under air

inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.01.033openalex-snapshot

The application of NCTS (N-cyano-N-phenyl-p-toluenesulfonamide) in palladium-catalyzed cyanation of arenediazonium tetrafluoroborates and aryl halides

inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.02.058openalex-snapshot

Carbonylative Hiyama coupling of aryl halides with arylsilanes under balloon pressure of CO

inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00163openalex-snapshot

Computational Studies of Synthetically Relevant Homogeneous Organometallic Catalysis Involving Ni, Pd, Ir, and Rh: An Overview of Commonly Employed DFT Methods and Mechanistic Insights

inferred← citeshttps://doi.org/10.1021/acs.joc.2c02858openalex-snapshot

Catalyst-Free Cascade Annulation of Enaminones and Aryl Diazonium Tetrafluoroboronates for Cinnoline Synthesis and the Anti-Inflammatory Activity Study

inferred← citeshttps://doi.org/10.1021/acs.joc.7b00140openalex-snapshot

Visible-Light-Promoted C–H Arylation by Merging Palladium Catalysis with Organic Photoredox Catalysis

inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02348openalex-snapshot

Palladium-Catalyzed Hiyama-Type Coupling of Thianthrenium and Phenoxathiinium Salts

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00098openalex-snapshot

Nickel-Catalyzed Stereospecific Alkylation of Vinylsiloxanes Using Pyridinium Salts

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00709openalex-snapshot

Palladium-Catalyzed Hiyama Cross-Coupling of Heterocyclic Phosphonium Salts with Arylsilanes

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03847openalex-snapshot

Palladium-Catalyzed Hiyama Cross-Coupling of Arylsulfonium Salts via C–S Bond Cleavage

inferred← citeshttps://doi.org/10.1021/acscatal.7b01415openalex-snapshot

A Generalized Picture of C–C Cross-Coupling

inferred← citeshttps://doi.org/10.1021/jo302791qopenalex-snapshot

Palladium-Catalyzed Hiyama-Type Cross-Coupling Reactions of Arenesulfinates with Organosilanes

inferred← citeshttps://doi.org/10.1021/ol501874sopenalex-snapshot

Rapid Synthesis of Crowded Aromatic Architectures from Silyl Acetylenes

inferred← citeshttps://doi.org/10.1021/om500452copenalex-snapshot

Mono- and Dinuclear Pincer Nickel Catalyzed Activation and Transformation of C–Cl, C–N, and C–O Bonds

inferred← citeshttps://doi.org/10.1039/c4qo00321gopenalex-snapshot

Highly efficient pincer nickel catalyzed cross-coupling of aryltrimethylammonium triflates with arylzinc reagents

inferred← citeshttps://doi.org/10.1039/c4ra04621hopenalex-snapshot

Palladium and copper-catalyzed ligand-free coupling of phenylhydrazines in water

inferred← citeshttps://doi.org/10.1039/c5ob00139kopenalex-snapshot

Palladium-catalyzed Hiyama coupling reaction of arylsulfonyl hydrazides under oxygen

inferred← citeshttps://doi.org/10.1039/c5ra01363aopenalex-snapshot

Pd-catalyzed desulfitative and denitrogenative Suzuki-type reaction of arylsulfonyl hydrazides

inferred← citeshttps://doi.org/10.1039/c6qo00634eopenalex-snapshot

Acid-promoted denitrogenative Pd-catalyzed addition of arylhydrazines with nitriles at room temperature

inferred← citeshttps://doi.org/10.1039/c7cc02830jopenalex-snapshot

Palladium-catalyzed dearomatizative [2 + 2 + 1] carboannulation of 1,7-enynes with aryl diazonium salts and H 2 O: facile synthesis of spirocyclohexadienone-fused cyclopenta[c]quinolin-4(5H)-ones

inferred← citeshttps://doi.org/10.1039/c8cs00453fopenalex-snapshot

Biaryl synthesis with arenediazonium salts: cross-coupling, CH-arylation and annulation reactions

inferred← citeshttps://doi.org/10.1039/c8ob00305jopenalex-snapshot

Denitrogenative palladium-catalyzed coupling of aryl halides with arylhydrazines under mild conditions

inferred← citeshttps://doi.org/10.1039/d2sc04482jopenalex-snapshot

Aryl diazonium intermediates enable mild DNA-compatible C–C bond formation for medicinally relevant combinatorial library synthesis

inferred← citeshttps://doi.org/10.1039/d6qo00973eopenalex-snapshot

Palladium-catalyzed direct dehydroxylative Hiyama-type cross-coupling of phenols with arylsilanes

inferred← citeshttps://doi.org/10.1055/s-0037-1611001openalex-snapshot

Palladium-Catalyzed Cross-Coupling of Arenediazonium Salts with Organoindium or Organobismuth Reagents

inferred← citeshttps://doi.org/10.1055/s-0040-1720112openalex-snapshot

Palladium-Catalyzed Amino-Sulfonylation of Aryl Iodide Derivatives via the Insertion of Sulfur Dioxide: One-Pot Synthesis of Aryl Primary Sulfonamides with Thiourea Dioxides

inferred← citeshttps://doi.org/10.1177/17475198211067163openalex-snapshot

Palladium-catalyzed Hiyama cross-couplings of pyrimidin-2-yl tosylates with organosilanes

inferred← citeshttps://doi.org/10.2174/1570179416666190412160048openalex-snapshot

A Green Approach for Organic Transformations Using Microwave Reactor

inferred← citeshttps://doi.org/10.3184/174751912x13496236042652openalex-snapshot

Fe(II)-Catalysed Homocoupling of Arenediazonium Tetrafluoroborates

inferred← citeshttps://doi.org/10.3390/molecules27175654openalex-snapshot

Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications

inferred← citeshttps://doi.org/10.5935/1984-6835.20140034openalex-snapshot

C-C Cross-Coupling: New Methodologies, Applications and Discoveries over the Last Few Years

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