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Palladium-Catalyzed Hiyama Cross-Couplings of Aryl Arenesulfonates with Arylsilanes

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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(20021018)41:20<3910::aid-anie3910>3.0.co;2-wopenalex-snapshot

Suzuki Cross-Couplings of Alkyl Tosylates that Possess β Hydrogen Atoms: Synthetic and Mechanistic Studies

inferredcites →https://doi.org/10.1002/9783527612222openalex-snapshot

Metal‐Catalyzed Cross‐Coupling Reactions

inferredcites →https://doi.org/10.1002/adsc.200404150openalex-snapshot

Room Temperature Nickel(0)‐Catalyzed Suzuki–Miyaura Cross‐Couplings of Activated Alkenyl Tosylates: Efficient Synthesis of 4‐Substituted Coumarins and 4‐Substituted 2(5H)‐ Furanones

inferredcites →https://doi.org/10.1002/adsc.200404196openalex-snapshot

First Microwave‐Accelerated Hiyama Coupling of Aryl‐ and Vinylsiloxane Derivatives: Clean Cross‐Coupling of Aryl Chlorides within Minutes

inferredcites →https://doi.org/10.1002/adsc.200404335openalex-snapshot

Transition Metal‐Catalyzed Cross‐Coupling and the Heck Coupling Processes: Powerful Reactions for Carbon‐Carbon and Carbon‐Heteroatom Bond Formation

inferredcites →https://doi.org/10.1002/adsc.200505494openalex-snapshot

Solvent‐Less and Fluoride‐Free Hiyama Reaction of Arylsiloxanes with Aryl Bromides and Chlorides Promoted by Sodium Hydroxide: A Useful Protocol for Palladium Recycling and Product Isolation

inferredcites →https://doi.org/10.1002/anie.200353015openalex-snapshot

Efficient Palladium‐Catalyzed Coupling of Aryl Chlorides and Tosylates with Terminal Alkynes: Use of a Copper Cocatalyst Inhibits the Reaction

inferredcites →https://doi.org/10.1002/anie.200700440openalex-snapshot

Hiyama Reactions of Activated and Unactivated Secondary Alkyl Halides Catalyzed by a Nickel/Norephedrine Complex

inferredcites →https://doi.org/10.1002/chem.200600034openalex-snapshot

Palladium‐Catalyzed Cross‐Coupling Reactions of Silanolates: A Paradigm Shift in Silicon‐Based Cross‐Coupling Reactions

inferredcites →https://doi.org/10.1016/0040-4039(94)02224-yopenalex-snapshot

6-Vinylated guanosine as a novel cross-linking agent and its versatile synthesis from the 6-O-tosylate by Pd(0)-catalyzed cross-coupling

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/b978-0-12-526550-8.x5001-1openalex-snapshot

Organoborane Chemistry

inferredcites →https://doi.org/10.1016/s0022-328x(02)01157-9openalex-snapshot

How I came across the silicon-based cross-coupling reaction

inferredcites →https://doi.org/10.1016/s0040-4039(01)02240-7openalex-snapshot

First examples of a tosylate in the palladium-catalyzed Heck cross coupling reaction

inferredcites →https://doi.org/10.1016/s0040-4039(02)01447-8openalex-snapshot

A copper-free palladium catalyzed cross coupling reaction of vinyl tosylates with terminal acetylenes

inferredcites →https://doi.org/10.1016/s0040-4039(99)02351-5openalex-snapshot

Tosylates in palladium-catalysed coupling reactions. Application to the synthesis of arylcoumarin inhibitors of gyrase B

inferredcites →https://doi.org/10.1021/ar020001ropenalex-snapshot

Design and Implementation of New, Silicon-Based, Cross-Coupling Reactions: Importance of Silicon−Oxygen Bonds

inferredcites →https://doi.org/10.1021/ar800036sopenalex-snapshot

Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands

inferredcites →https://doi.org/10.1021/ja015655uopenalex-snapshot

Palladium-Catalyzed Cross-Coupling Reaction of Alkenyldimethyl(2-pyridyl)silanes with Organic Halides: Complete Switch from the Carbometalation Pathway to the Transmetalation Pathway

inferredcites →https://doi.org/10.1021/ja027190topenalex-snapshot

Iron-Catalyzed Cross-Coupling Reactions

inferredcites →https://doi.org/10.1021/ja0349352openalex-snapshot

Room-Temperature Hiyama Cross-Couplings of Arylsilanes with Alkyl Bromides and Iodides

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/ja0639719openalex-snapshot

The Selective Reaction of Aryl Halides with KOH: Synthesis of Phenols, Aromatic Ethers, and Benzofurans

inferredcites →https://doi.org/10.1021/jo00049a047openalex-snapshot

Palladium-catalyzed coupling of aryl arenesulfonates with organostannanes

inferredcites →https://doi.org/10.1021/jo00109a044openalex-snapshot

Aryl Mesylates in Metal Catalyzed Homocoupling and Cross-Coupling Reactions. 2. Suzuki-Type Nickel-Catalyzed Cross-Coupling of Aryl Arenesulfonates and Aryl Mesylates with Arylboronic Acids

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/jo051394lopenalex-snapshot

Kumada Coupling of Aryl and Vinyl Tosylates under Mild Conditions

inferredcites →https://doi.org/10.1021/jo051590sopenalex-snapshot

Enol Tosylates as Viable Partners in Pd-Catalyzed Cross-Coupling Reactions

inferredcites →https://doi.org/10.1021/jo051636hopenalex-snapshot

Efforts Directed toward the Synthesis of Colchicine: Application of Palladium-Catalyzed Siloxane Cross-Coupling Methodology

inferredcites →https://doi.org/10.1021/jo7019064openalex-snapshot

Palladium-Catalyzed Suzuki−Miyaura Cross-Couplings of Aryl Tosylates with Potassium Aryltrifluoroborates

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/ol025673wopenalex-snapshot

Facile Pd-Catalyzed Cross-Coupling of 2‘-Deoxyguanosine O6-Arylsulfonates with Arylboronic Acids

inferredcites →https://doi.org/10.1021/ol047854zopenalex-snapshot

Stereoselective Enol Tosylation: Preparation of Trisubstituted α,β-Unsaturated Esters

inferredcites →https://doi.org/10.1021/ol049851sopenalex-snapshot

Palladium−Phosphinous Acid-Catalyzed NaOH-Promoted Cross-Coupling Reactions of Arylsiloxanes with Aryl Chlorides and Bromides in Water

inferredcites →https://doi.org/10.1021/ol052517ropenalex-snapshot

Vinylation of Aryl Bromides Using an Inexpensive Vinylpolysiloxane

inferredcites →https://doi.org/10.1021/ol061116oopenalex-snapshot

Air-Stable PinP(O)H as Preligand for Palladium-Catalyzed Kumada Couplings of Unactivated Tosylates

inferredcites →https://doi.org/10.1039/b518283bopenalex-snapshot

Cross-coupling reactions of aryl and vinyl chlorides catalyzed by a palladium complex derived from an air-stable H-phosphonate

inferredcites →https://doi.org/10.1055/s-1999-2643openalex-snapshot

Alternatives to Vinyl Triflates for Cross-Coupling with Arylboronic Acids

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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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/10.1002/047084289x.rn00923.pub2openalex-snapshot

Bis(1,1-dimethylethyl)[2′,4′,6′-tris-(1-methylethyl)[1,1′-biphenyl]-2-yl]-phosphine and Dicyclohexyl[2′,4′,6′-tris(1-methylethyl)[1,1′-biphenyl]-2-yl]phosphine

inferred← citeshttps://doi.org/10.1002/047084289x.rn00923.pub4openalex-snapshot

Bis(1,1‐dimethylethyl)[2′,4′,6′‐tris‐(1‐methylethyl)[1,1′‐biphenyl]‐2‐yl]‐phosphine and Dicyclohexyl[2′,4′,6′‐tris(1‐methylethyl)[1,1′‐biphenyl]‐2‐yl]phosphine

inferred← citeshttps://doi.org/10.1002/0471264180.or075.03openalex-snapshot

Cross‐Coupling with Organosilicon Compounds

inferred← citeshttps://doi.org/10.1002/9780471264194.fos11654.pub2openalex-snapshot

Palladium( II ) Acetate – Tertiary Phosphine

inferred← citeshttps://doi.org/10.1002/9780471264194.fos11654.pub3openalex-snapshot

Palladium( II ) Acetate – Tertiary Phosphine

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Selected Applications of Transition Metal‐Catalyzed Carbon–Carbon Cross‐Coupling Reactions in the Pharmaceutical Industry

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Formation of Alkanes and Arenes by Coupling Reactions

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Homogeneous Transition‐Metal‐Catalyzed C–O Bond Activation

inferred← citeshttps://doi.org/10.1002/9783527633678.ch5openalex-snapshot

Silicon‐Based Carbon–Carbon Bond Formation by Transition Metal Catalysis

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

Transition‐Metal‐Catalyzed Cross‐coupling of Organosilicon Compounds

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Pd ‐Catalyzed C C Bond‐Forming Reactions

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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

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Palladium‐Catalyzed Fluoride‐Free Cross‐Coupling of Intramolecularly Activated Alkenylsilanes and Alkenylgermanes: Synthesis of Tamoxifen as a Synthetic Application

inferred← citeshttps://doi.org/10.1002/adsc.201600590openalex-snapshot

Nickel‐ or Iron‐Catalyzed Cross‐Coupling of Aryl Carbamates with Arylsilanes

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Palladium‐Catalyzed One‐Pot Synthesis of C2‐Quaternary Indolin‐3‐ones via 1H‐indole‐3‐sulfonates Generated in Situ from 2‐Alkynyl Arylazides and Sulfonic Acids

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Nickel‐Catalyzed C(sp2)−C(sp3) Kumada Cross‐Coupling of Aryl Tosylates with Alkyl Grignard Reagents

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Pd‐Catalyzed Ring‐Opening Defluorinative Arylation of gem‐Difluorocyclopropanes with Arylsilanes

inferred← citeshttps://doi.org/10.1002/ajoc.201300031openalex-snapshot

Aryl[2‐(hydroxypro‐2‐yl)cyclohyxyl]dimethylsilane: A Robust Aryl(trialkyl)silane Reagent for Nickel‐catalyzed Cross‐coupling Reactions with Aryl Tosylates

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

inferred← citeshttps://doi.org/10.1002/ange.200803814openalex-snapshot

Cross‐Coupling of Aryl/Alkenyl Pivalates with Organozinc Reagents through Nickel‐Catalyzed CO Bond Activation under Mild Reaction Conditions

inferred← citeshttps://doi.org/10.1002/ange.200901884openalex-snapshot

Palladium‐Catalyzed Direct Arylation of Cyclic Enamides with Aryl Silanes by sp2 CH Activation

inferred← citeshttps://doi.org/10.1002/ange.200906996openalex-snapshot

Nickel‐Catalyzed Direct CH Arylation and Alkenylation of Heteroarenes with Organosilicon Reagents

inferred← citeshttps://doi.org/10.1002/ange.200907359openalex-snapshot

Direct Application of Phenolic Salts to Nickel‐Catalyzed Cross‐Coupling Reactions with Aryl Grignard Reagents

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Rearrangement of 2‐Aryloxybenzaldehydes to 2‐Hydroxybenzophenones by Rhodium‐Catalyzed Cleavage of Aryloxy CO Bonds

inferred← citeshttps://doi.org/10.1002/ange.201108154openalex-snapshot

Palladium‐Catalyzed Intermolecular Coupling of 2‐Silylaryl Bromides with Alkynes: Synthesis of Benzosiloles and Heteroarene‐Fused Siloles by Catalytic Cleavage of the C(sp3)Si Bond

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Cross‐Coupling of Aryl/Alkenyl Pivalates with Organozinc Reagents through Nickel‐Catalyzed CO Bond Activation under Mild Reaction Conditions

inferred← citeshttps://doi.org/10.1002/anie.200901884openalex-snapshot

Palladium‐Catalyzed Direct Arylation of Cyclic Enamides with Aryl Silanes by sp2 CH Activation

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Transition‐Metal‐Catalyzed Direct Arylation of (Hetero)Arenes by CH Bond Cleavage

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Nickel‐Catalyzed Direct CH Arylation and Alkenylation of Heteroarenes with Organosilicon Reagents

inferred← citeshttps://doi.org/10.1002/anie.200907359openalex-snapshot

Direct Application of Phenolic Salts to Nickel‐Catalyzed Cross‐Coupling Reactions with Aryl Grignard Reagents

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Rearrangement of 2‐Aryloxybenzaldehydes to 2‐Hydroxybenzophenones by Rhodium‐Catalyzed Cleavage of Aryloxy CO Bonds

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Palladium‐Catalyzed Intermolecular Coupling of 2‐Silylaryl Bromides with Alkynes: Synthesis of Benzosiloles and Heteroarene‐Fused Siloles by Catalytic Cleavage of the C(sp 3 )Si Bond

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Application of a dimeric ortho‐palladated complex of tribenzylamine as an efficient catalyst in microwave‐assisted Hiyama coupling reactions

inferred← citeshttps://doi.org/10.1002/aoc.5140openalex-snapshot

Desulfinative palladium‐catalyzed cross‐coupling of arylsulfonyl hydrazides with aryl bromides under air

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A comparative study of catalytic activity on iron‐based carbon nanostructured catalysts with Pd loading: Using the Box–Behnken design (BBD) method in the Suzuki–Miyaura coupling

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Recent advances in palladium‐catalyzed α‐arylation reactions

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Magnetic Pd– Fe3O4 Heterodimer Nanocrystals as Recoverable Catalysts for Ligand‐Free Hiyama Cross‐Coupling Reactions

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Cobalt−NHC Catalyzed C(sp2)−C(sp3) and C(sp2)−C(sp2) Kumada Cross‐Coupling of Aryl Tosylates with Alkyl and Aryl Grignard Reagents

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Aryl Phosphoramides: Useful Electrophiles for Suzuki–Miyaura Coupling Catalyzed by a NiCl2/dppp System (dppp=1,3‐Bis(diphenylphosphino)propane)

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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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Chemodivergence between Electrophiles in Cross‐Coupling Reactions

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ChemInform Abstract: Palladium‐Catalyzed Hiyama Cross‐Couplings of Aryl Arenesulfonates with Arylsilanes.

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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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2‐Pyridyl Tosylate Derivatives—Building Blocks for Structural Diversity via Transition Metal Catalysis

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

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Palladium (II) Catalyzed Arylation and Methylene Oxidation of 2, 7‐Dibromo Fluorenes with Heteroaryl Esters: Synthesis of Mesogenic2‐Heteroaryl and 2, 7‐Diheteroaryl‐9‐fluorenones

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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

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Recent Advances in Cross-Coupling Reactions with Aryl Chlorides, Tosylates, and Mesylates

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Highly Efficient Pd-Catalyzed Cyanation of Aryl Chlorides and Arenesulfonates with Potassium Ferrocyanide in Aqueous Media

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

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Cross-Coupling Reactions

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Palladium(II) complexes of anthraquinone-based As–O–As type and Se–O–Se type bipodands. Synthesis, X-ray crystallography and catalytic properties

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NHC–Pd(II)–Im (NHC = N-heterocyclic carbene; Im = 1-methylimidazole) complex catalyzed Hiyama reaction of aryl chlorides with aryltrimethoxysilanes

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Pd(II)-catalyzed ortho arylation of 2-arylbenzothiazoles with aryl iodides via benzothiazole-directed C–H activation

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Supported phosphine free bis-NHC palladium pincer complex: An efficient reusable nanocatalyst for Suzuki-Miyaura coupling reaction

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Palladium(II) and Ruthenium(II) complexes bearing arylsulfonate based ligands: Synthesis, structural characterization and catalytic properties

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Pd-catalyzed decarboxylative couplings of arenecarboxylic acids with aryl iodides

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Manganese(III) acetate-mediated synthesis of biaryls under microwave irradiation

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Rapid access to 4-substituted-pyrones and 2(5H)-furanones via a palladium-catalyzed C–OH bond activation

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A atom-efficient cross-coupling reaction of aryl iodides with triarylbismuths catalyzed by immobilization of palladium(II)-Schiff base complex in MCM-41

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Palladium catalyzed desulfinylative couplings between aryl sulfinates and aryl bromide/iodide for the synthesis of biaryls

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Nucleophilic disulfurating reagents for unsymmetrical disulfides construction via copper-catalyzed oxidative cross coupling

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Palladium-catalyzed direct arylation of 4-hydroxycoumarins with arylboronic acids via C–OH bond activation

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An efficient route to 4-substituted coumarins, 2(5H)-furanones, and pyrones via palladium-catalyzed couplings of alkenyl tosylates with organoindium reagents

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Copper-free palladium-catalyzed Sonogashira and Hiyama cross-couplings using aryl imidazol-1-ylsulfonates

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Palladium-catalyzed cross-coupling reaction of aryl(trialkyl)silanes with aryl nitriles

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

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

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Desulfinylative Pd-catalyzed coupling reaction of arenediazonium salt with aryl sulfinates to give unsymmetrical biaryls

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Unified Protocol for Fe-Based Catalyzed Biaryl Cross-Couplings between Various Aryl Electrophiles and Aryl Grignard Reagents

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

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Rh(I)-Catalyzed Cross-Coupling of α-Diazoesters with Arylsiloxanes

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Diversity-Oriented Stereoselective Synthesis of β,γ-Disubstituted tert-Homoallylic Alcohols

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Pd(II)-Catalyzed C3-Selective Arylation of Pyridine with (Hetero)arenes

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

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Palladium-Catalyzed Hiyama Cross-Coupling of Aryl Fluorosulfates

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Transition-Metal-Catalyzed Transformation of Sulfonates via S–O Bond Cleavage: Synthesis of Alkyl Aryl Ether and Diaryl Ether

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General Chemoselective Suzuki–Miyaura Coupling of Polyhalogenated Aryl Triflates Enabled by an Alkyl-Heteroaryl-Based Phosphine Ligand

inferred← citeshttps://doi.org/10.1021/acscatal.6b02964openalex-snapshot

An Adventure in Sustainable Cross-Coupling of Phenols and Derivatives via Carbon–Oxygen Bond Cleavage

inferred← citeshttps://doi.org/10.1021/acssuschemeng.8b00598openalex-snapshot

NCN–Pincer–Pd Complex as Catalyst for the Hiyama Reaction in Biomass-Derived Solvents

inferred← citeshttps://doi.org/10.1021/ar100082dopenalex-snapshot

Exploration of New C−O Electrophiles in Cross-Coupling Reactions

inferred← citeshttps://doi.org/10.1021/cr100412jopenalex-snapshot

Carboxylate-Assisted Transition-Metal-Catalyzed C−H Bond Functionalizations: Mechanism and Scope

inferred← citeshttps://doi.org/10.1021/ja2024959openalex-snapshot

Palladium-Catalyzed Synthesis of Benzosilolo[2,3-b]indoles via Cleavage of a C(sp3)–Si Bond and Consequent Intramolecular C(sp2)–Si Coupling

inferred← citeshttps://doi.org/10.1021/jacs.6b04018openalex-snapshot

Catalytic Reductive ortho -C–H Silylation of Phenols with Traceless, Versatile Acetal Directing Groups and Synthetic Applications of Dioxasilines

inferred← citeshttps://doi.org/10.1021/jo100926aopenalex-snapshot

Copper-Catalyzed Sequential Alkyl/Aryl or Vinyl Esterification of Dicarboxylic Acid Anhydrides with Alkoxysilanes

inferred← citeshttps://doi.org/10.1021/jo201840nopenalex-snapshot

Palladium-Catalyzed Hiyama Cross-Coupling of Aryltrifluorosilanes with Aryl and Heteroaryl Chlorides

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/ol101147bopenalex-snapshot

Pd(OAc)2-Catalyzed Regioselective Arylation of Indoles with Arylsiloxane in Acidic Medium

inferred← citeshttps://doi.org/10.1021/ol200267bopenalex-snapshot

Palladium- and Nickel-Catalyzed Aminations of Aryl Imidazolylsulfonates and Sulfamates

inferred← citeshttps://doi.org/10.1021/ol303130jopenalex-snapshot

Iron-Catalyzed Cross-Coupling Reactions of Alkyl Grignards with Aryl Sulfamates and Tosylates

inferred← citeshttps://doi.org/10.1021/ol4022904openalex-snapshot

Phosphine-Catalyzed Domino Benzannulation: An Efficient Method to Construct Biaryl Skeletons

inferred← citeshttps://doi.org/10.1021/ol5018849openalex-snapshot

A Copper-Catalyzed Three-Component Reaction of Triethoxysilanes, Sulfur Dioxide, and Hydrazines

inferred← citeshttps://doi.org/10.1021/ol5024344openalex-snapshot

Iron-Catalyzed Coupling of Aryl Sulfamates and Aryl/Vinyl Tosylates with Aryl Grignards

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/ol9029534openalex-snapshot

Nickel-Catalyzed Efficient and Practical Suzuki−Miyaura Coupling of Alkenyl and Aryl Carbamates with Aryl Boroxines

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/10.1038/s41467-024-47205-8openalex-snapshot

Trialkoxysilane-Induced Iridium-Catalyzed para-Selective C–H Bond Borylation of Arenes

inferred← citeshttps://doi.org/10.1039/b821870fopenalex-snapshot

Palladium-catalyzed decarboxylative cross-coupling reaction of cinnamic acid with aryl iodide

inferred← citeshttps://doi.org/10.1039/b903285aopenalex-snapshot

Synthesis of tetra- and pentacoordinate palladium complexes of functionalized N-heterocyclic carbenes and a comparative study of their catalytic activities

inferred← citeshttps://doi.org/10.1039/b917777aopenalex-snapshot

Direct dehydrative cross-coupling of tautomerizable heterocycles with alkynes via Pd/Cu-catalyzed phosphonium coupling

inferred← citeshttps://doi.org/10.1039/c0cc02173copenalex-snapshot

Nickel-catalysed cross-coupling reaction of aryl(trialkyl)silanes with aryl chlorides and tosylates

inferred← citeshttps://doi.org/10.1039/c0cc02360dopenalex-snapshot

Direct arylations of electron-deficient (hetero)arenes with aryl or alkenyl tosylates and mesylates

inferred← citeshttps://doi.org/10.1039/c0cc03107kopenalex-snapshot

A pyridine-bridged bis-benzimidazolylidene pincer nickel(ii) complex: synthesis and practical catalytic application towards Suzuki–Miyaura coupling with less-activated electrophiles

inferred← citeshttps://doi.org/10.1039/c0cc03535aopenalex-snapshot

General and highly active catalyst for mono and double Hiyama coupling reactions of unreactive aryl chlorides in water

inferred← citeshttps://doi.org/10.1039/c0gc00122hopenalex-snapshot

Highly effective alternative aryl trihydroxyborate salts for a ligand-free, on-water Suzuki–Miyaura coupling reaction

inferred← citeshttps://doi.org/10.1039/c0nj01019gopenalex-snapshot

An easy access to styrenes: trans aryl 1,3-, 1,4- and 1,5-dienes, and 1,3,5-trienes by Hiyama cross-coupling catalyzed by palladium nanoparticles

inferred← citeshttps://doi.org/10.1039/c0ob00212gopenalex-snapshot

Regioselective syntheses of fully-substituted 1,2,3-triazoles: the CuAAC/C–H bond functionalization nexus

inferred← citeshttps://doi.org/10.1039/c1cs15114bopenalex-snapshot

Palladium-catalyzed cross-coupling reactions of aryl mesylates

inferred← citeshttps://doi.org/10.1039/c1cs15122copenalex-snapshot

Silicon-based cross-coupling reaction: an environmentally benign version

inferred← citeshttps://doi.org/10.1039/c1cs15181aopenalex-snapshot

Palladium-catalysed cross-coupling of organosilicon reagents

inferred← citeshttps://doi.org/10.1039/c1sc00356aopenalex-snapshot

Opening the silole ring: Efficient and specific cleavage of the endo-C(sp2)-Si bond with AcOH/ROH system

inferred← citeshttps://doi.org/10.1039/c2dt31174gopenalex-snapshot

Synthesis and characterization of dinuclear NHC–palladium complexes and their applications in the Hiyama reactions of aryltrialkyoxysilanes with aryl chlorides

inferred← citeshttps://doi.org/10.1039/c3cc41421copenalex-snapshot

Palladium-catalyzed Suzuki cross-coupling of N′-tosyl arylhydrazines

inferred← citeshttps://doi.org/10.1039/c3dt51119gopenalex-snapshot

Keggin type mono Ni(ii)-substituted phosphomolybdate: a sustainable, homogeneous and reusable catalyst for Suzuki–Miyaura cross-coupling

inferred← citeshttps://doi.org/10.1039/c3dt53391copenalex-snapshot

DFT studies on the mechanism of palladium-catalyzed carbon–silicon cleavage for the synthesis of benzosilole derivatives

inferred← citeshttps://doi.org/10.1039/c4cy00256copenalex-snapshot

Nanoporous palladium catalyzed silicon-based one-pot cross-coupling reaction of aryl iodides with organosilanes

inferred← citeshttps://doi.org/10.1039/c4gc00141aopenalex-snapshot

Efficient ligand-free Hiyama cross-coupling reaction catalyzed by functionalized SBA-15-supported Pd nanoparticles

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

Palladium-catalyzed Hiyama coupling reaction of arylsulfonyl hydrazides under oxygen

inferred← citeshttps://doi.org/10.1039/c5ob02514aopenalex-snapshot

A palladium-catalyzed coupling reaction of aryl nonaflates, sulfur dioxide, and hydrazines

inferred← citeshttps://doi.org/10.1039/c5ra12512jopenalex-snapshot

Synthesis of benzochromenes and dihydrophenanthridines with helical motifs using Garratt–Braverman and Buchwald–Hartwig reactions

inferred← citeshttps://doi.org/10.1039/c6qo00589fopenalex-snapshot

Rhodium( iii )-catalyzed directed C–H benzylation and allylation of indoles with organosilicon reagents

inferred← citeshttps://doi.org/10.1039/c7dt01433copenalex-snapshot

Synthesis of zwitterionic palladium complexes and their application as catalysts in cross-coupling reactions of aryl, heteroaryl and benzyl bromides with organoboron reagents in neat water

inferred← citeshttps://doi.org/10.1039/c7ob00818jopenalex-snapshot

Ruthenium( ii )-catalyzed ortho-C–H arylation of diverse N-heterocycles with aryl silanes by exploiting solvent-controlled N-coordination

inferred← citeshttps://doi.org/10.1039/c7ob02531aopenalex-snapshot

Efficient cross-coupling of aryl/alkenyl triflates with acyclic secondary alkylboronic acids

inferred← citeshttps://doi.org/10.1039/c7sc00156hopenalex-snapshot

Highly chemoselective ruthenium( ii )-catalyzed direct arylation of cyclic and N,N-dialkyl benzamides with aryl silanes

inferred← citeshttps://doi.org/10.1039/d0cy01159bopenalex-snapshot

Palladium-catalyzed cross-couplings by C–O bond activation

inferred← citeshttps://doi.org/10.1039/d0gc01494jopenalex-snapshot

Deep eutectic solvents: cutting-edge applications in cross-coupling reactions

inferred← citeshttps://doi.org/10.1039/d0ob01718copenalex-snapshot

An update on the use of sulfinate derivatives as versatile coupling partners in organic chemistry

inferred← citeshttps://doi.org/10.1039/d1ob01202aopenalex-snapshot

Silicon compounds in carbon-11 radiochemistry: present use and future perspectives

inferred← citeshttps://doi.org/10.1039/d5qo01479dopenalex-snapshot

TBADT/nickel co-catalyzed arylation of hydrosilanes with aryl halides

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/a-1503-6330openalex-snapshot

C–O-Selective Cross-Coupling of Chlorinated Phenol Derivatives

inferred← citeshttps://doi.org/10.1080/17415993.2015.1057512openalex-snapshot

Synthesis and reactivity of imidazole-1-sulfonate esters (imidazylates) in substitution, elimination, and metal-catalyzed cross-coupling reactions: a review

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

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

inferred← citeshttps://doi.org/10.1246/cl.160439openalex-snapshot

Silicon-based Cross-coupling of Aryl Tosylates by Cooperative Palladium/Copper Catalysis

inferred← citeshttps://doi.org/10.1246/cl.181018openalex-snapshot

Cross-coupling Reaction of Aryl(triethyl)silanes with Aryl Chlorides: An Easy Access to Oligothiophenes

inferred← citeshttps://doi.org/10.1246/cl.2011.1001openalex-snapshot

Cross-coupling of Aryl/Alkenyl Silyl Ethers with Grignard Reagents through Nickel-catalyzed C–O Bond Activation

inferred← citeshttps://doi.org/10.1246/cl.2012.1503openalex-snapshot

Synthesis of Unsymmetrical Diarylethynes by Pd(0)/Cu(I)-cocatalyzed Sila-Sonogashira–Hagihara Coupling Reactions of Alkynylsilanes with Aryl Tosylates or Mesylates

inferred← citeshttps://doi.org/10.1351/pac-con-09-08-17openalex-snapshot

Transition-metal-catalyzed direct arylations via C–H bond cleavages

inferred← citeshttps://doi.org/10.1515/9783111739601-022openalex-snapshot

73121 Hiyama cross-coupling reactions

inferred← citeshttps://doi.org/10.17760/d20000131openalex-snapshot

The development of a versatile and expeditious route to pet imaging ligands and its potential applications to prostate cancer treatment and diagnosis

inferred← citeshttps://doi.org/10.2174/1385272827666230217093032openalex-snapshot

Progress in the Preparation and Application of Arylsilane

inferred← citeshttps://doi.org/10.24820/ark.5550190.p011.845openalex-snapshot

Recent advances and prospects in palladium-catalyzed Hiyama coupling reaction

inferred← citeshttps://doi.org/10.3762/bxiv.2023.25.v1openalex-snapshot

Modulating the electronics of palladium complexes supported by iminopyridine ligands as the catalysts in Suzuki-Miyaura and Heck-Mizoroki cross-coupling reactions

inferred← citeshttps://doi.org/10.5012/bkcs.2010.31.01.025openalex-snapshot

Cross-coupling Reaction of β,β-Difluoro-α-phenylvinylstannane with Alkenyl Iodides: Novel Approach to 2-Phenyl-1,1-difluoro-1,3-butadienes

inferred← citeshttps://doi.org/10.5012/bkcs.2010.31.01.250openalex-snapshot

Silica-Supported Palladium-Catalyzed Hiyama Cross-Coupling Reactions Using Continuous Flow System

inferred← citeshttps://doi.org/10.70675/1bc9a11fzd9dcz47a7z8004zc8985462b86eopenalex-snapshot

Activation et transformation catalytique de SO₂ par des composés organométalliques et organiques

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