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Palladium−Imidazolium Carbene Catalyzed Aryl, Vinyl, and Alkyl Suzuki−Miyaura Cross Coupling
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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/anie.199628051openalex-snapshot
Chiral Heterocylic Carbenes in Asymmetric Homogeneous Catalysis
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(99)00927-8openalex-snapshot
Imidazolylidenes, imidazolinylidenes and imidazolidines
inferredcites →https://doi.org/10.1016/s0040-4039(00)93420-8openalex-snapshot
One-pot synthesis of cyclic amidinium tetrafluoroborates and hexafluorophosphates; the simplest models of N5,N100methenyltetrahydrofolate coenzyme
inferredcites →https://doi.org/10.1021/ja0002058openalex-snapshot
Versatile Catalysts for the Suzuki Cross-Coupling of Arylboronic Acids with Aryl and Vinyl Halides and Triflates under Mild Conditions
inferredcites →https://doi.org/10.1021/ja00183a048openalex-snapshot
Palladium-catalyzed inter- and intramolecular cross-coupling reactions of B-alkyl-9-borabicyclo[3.3.1]nonane derivatives with 1-halo-1-alkenes or haloarenes. Syntheses of functionalized alkenes, arenes, and cycloalkenes via a hydroboration-coupling sequence
inferredcites →https://doi.org/10.1021/ja005613qopenalex-snapshot
Thiol Ester−Boronic Acid Coupling. A Mechanistically Unprecedented and General Ketone Synthesis
inferredcites →https://doi.org/10.1021/ja982250+openalex-snapshot
A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides
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/ja992130hopenalex-snapshot
Highly Active Palladium Catalysts for Suzuki Coupling Reactions
inferredcites →https://doi.org/10.1021/jo00434a018openalex-snapshot
Alkyl nitrite-metal halide deamination reactions. 3. Arylation of olefinic compounds in the deamination of arylamines by alkyl nitrites and copper(II) halides. A convenient and effective variation of the Meerwein arylation reaction
inferredcites →https://doi.org/10.1021/jo960058popenalex-snapshot
Palladium-Catalyzed Cross-Coupling of Arenediazonium Salts with Arylboronic Acids
inferredcites →https://doi.org/10.1021/jo990554oopenalex-snapshot
Palladium−Imidazol-2-ylidene Complexes as Catalysts for Facile and Efficient Suzuki Cross-Coupling Reactions of Aryl Chlorides with Arylboronic Acids
inferredcites →https://doi.org/10.1021/ol005956topenalex-snapshot
Efficient Cross-Coupling Reactions of Aryl Chlorides and Bromides with Phenyl- or Vinyltrimethoxysilane Mediated by a Palladium/Imidazolium Chloride System
inferredcites →https://doi.org/10.1021/ol0062547openalex-snapshot
Transannular Macrocyclization via Intramolecular B-Alkyl Suzuki Reaction
inferredcites →https://doi.org/10.1021/ol006827fopenalex-snapshot
Palladium/Imidazolium Salt Catalyzed Coupling of Aryl Halides with Hypervalent Organostannates
inferredcites →https://doi.org/10.1021/ol010060popenalex-snapshot
Nonbasic, Room Temperature, Palladium-Catalyzed Coupling of Aryl and Alkenyl Iodides with Boronic Acids Mediated by Copper(I) Thiophene-2-carboxylate (CuTC)
inferredcites →https://doi.org/10.1021/ol015676topenalex-snapshot
Convenient and Efficient Suzuki−Miyaura Cross-Coupling Catalyzed by a Palladium/Diazabutadiene System
inferredcites →https://doi.org/10.1021/ol015827sopenalex-snapshot
Highly Efficient Heck Reactions of Aryl Bromides with n-Butyl Acrylate Mediated by a Palladium/Phosphine−Imidazolium Salt System
inferredcites →https://doi.org/10.1021/ol990909qopenalex-snapshot
Synthesis and Activity of a New Generation of Ruthenium-Based Olefin Metathesis Catalysts Coordinated with 1,3-Dimesityl-4,5-dihydroimidazol-2-ylidene Ligands
inferredcites →https://doi.org/10.1021/om970826iopenalex-snapshot
Chiral Oxazoline/Imidazoline-2-ylidene Complexes
inferredcites →https://doi.org/10.1021/om990776copenalex-snapshot
Donor-Functionalized Heterocyclic Carbene Complexes of Palladium(II): Efficient Catalysts for C−C Coupling Reactions
inferredcites →https://doi.org/10.1055/s-1998-1590openalex-snapshot
Suzuki Reactions with B-Allyl-9-Borabicyclo[3.3.1]nonane (B-Allyl-9-BBN)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/047084289x.rn00291openalex-snapshot
1,3-bis(2,6-diisopropylphenyl)-4,5-dihydroimidazol-2-ylidene
inferred← citeshttps://doi.org/10.1002/047084289x.rn00291.pub2openalex-snapshot
1,3-bis(2,6-diisopropylphenyl)-4,5-dihydroimidazol-2-ylidene
inferred← citeshttps://doi.org/10.1002/0471264229.os088.20openalex-snapshot
Discussion Addendum for: Palladium(0)‐Catalyzed Reaction of 9‐Alkyl‐9‐Borabicyclo[3.3.1]Nonane with 1‐Bromo‐1‐Phenylthioethene: 4‐(3‐Cyclohexenyl)‐2‐Phenylthio‐1‐Butene
inferred← citeshttps://doi.org/10.1002/9780470503973.ch5openalex-snapshot
Preparation of Alkyls, Methylenes, and Aryls
inferred← citeshttps://doi.org/10.1002/9780471264194.fos07552.pub2openalex-snapshot
Palladium(II) acetate
inferred← citeshttps://doi.org/10.1002/9780471264194.fos07552.pub3openalex-snapshot
Palladium(II) acetate
inferred← citeshttps://doi.org/10.1002/9780471264194.fos07552.pub4openalex-snapshot
Palladium( II ) Acetate
inferred← citeshttps://doi.org/10.1002/9780471264194.fos07552.pub5openalex-snapshot
Palladium( II ) Acetate
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/10.1002/9780471264194.fos11766openalex-snapshot
Palladium( II ) Acetate – Aminocarbene
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11766.epub2openalex-snapshot
Palladium – aminocarbene complexes
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11766.pub3openalex-snapshot
Palladium – aminocarbene complexes
inferred← citeshttps://doi.org/10.1002/9780471476665.ch5openalex-snapshot
Preparation of Alkyls, Methylenes and Aryls
inferred← citeshttps://doi.org/10.1002/9781118662083.cot01-002openalex-snapshot
Formation of Alkanes and Arenes by Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9783527619535.ch2openalex-snapshot
Metal‐Catalyzed Cross‐Coupling Reactions of Organoboron Compounds with Organic Halides
inferred← citeshttps://doi.org/10.1002/adsc.200404212openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling Reaction of 1‐Aryltriazenes with Aryl‐ and Alkenyltrifluorosilanes
inferred← citeshttps://doi.org/10.1002/adsc.200505409openalex-snapshot
Nickel(0)/Imidazolium Carbene Catalyst System for Efficient Cross‐Coupling of Aryl Bromides and Chlorides with Organomanganese Reagents
inferred← citeshttps://doi.org/10.1002/adsc.200800162openalex-snapshot
Suzuki–Miyaura Cross‐Coupling of 2‐Nitroarenediazonium Tetrafluoroborates: Synthesis of Unsymmetrical 2‐Nitrobiphenyls and Highly Functionalized Carbazoles
inferred← citeshttps://doi.org/10.1002/adsc.200800630openalex-snapshot
Direct B‐Alkyl Suzuki–Miyaura Cross‐Coupling of Trialkyl‐ boranes with Aryl Bromides in the Presence of Unmasked Acidic or Basic Functions and Base‐Labile Protections under Mild Non‐Aqueous Conditions
inferred← citeshttps://doi.org/10.1002/adsc.201100531openalex-snapshot
Aryl Diazonium versus Iodonium Salts: Preparation, Applications and Mechanisms for the Suzuki–Miyaura Cross‐Coupling Reaction
inferred← citeshttps://doi.org/10.1002/adsc.70542openalex-snapshot
Decoding Transmetalation in Miyaura Borylation: The Hidden Chemistry of Bis(pinacolato) Diboron and Base Effects
inferred← citeshttps://doi.org/10.1002/ajoc.201500063openalex-snapshot
Silver‐Nitrite‐Assisted In Situ Diazotization Reaction: Cross‐Coupling of Anilines with Arylboronic Acids at Room Temperature
inferred← citeshttps://doi.org/10.1002/ajoc.202100437openalex-snapshot
Nickel Catalyzed Ligand‐ And Base‐Free One‐Pot Diazotization/Cross‐Coupling of Aryl Amine With Aryl Boronic Acid
inferred← citeshttps://doi.org/10.1002/ange.200352679openalex-snapshot
Asymmetric Addition of Aryl Boron Reagents to Enones with Rhodium Dicyclophane Imidazolium Carbene Catalysis
inferred← citeshttps://doi.org/10.1002/ange.200601663openalex-snapshot
Aus der Sicht des Synthetikers: Palladiumkomplexe N‐heterocyclischer Carbene als Katalysatoren für Kreuzkupplungen
inferred← citeshttps://doi.org/10.1002/ange.201106299openalex-snapshot
Alkylboronic Esters from Copper‐Catalyzed Borylation of Primary and Secondary Alkyl Halides and Pseudohalides
inferred← citeshttps://doi.org/10.1002/ange.201702107openalex-snapshot
Enantioselective Heck–Matsuda Arylations through Chiral Anion Phase‐Transfer of Aryl Diazonium Salts
inferred← citeshttps://doi.org/10.1002/ange.202504012openalex-snapshot
Nitrate Reduction for Deaminative Suzuki–Miyaura Coupling of Anilines
inferred← citeshttps://doi.org/10.1002/anie.200352679openalex-snapshot
Asymmetric Addition of Aryl Boron Reagents to Enones with Rhodium Dicyclophane Imidazolium Carbene Catalysis
inferred← citeshttps://doi.org/10.1002/anie.200601663openalex-snapshot
Palladium Complexes of N‐Heterocyclic Carbenes as Catalysts for Cross‐Coupling Reactions—A Synthetic Chemist's Perspective
inferred← citeshttps://doi.org/10.1002/anie.201106299openalex-snapshot
Alkylboronic Esters from Copper‐Catalyzed Borylation of Primary and Secondary Alkyl Halides and Pseudohalides
inferred← citeshttps://doi.org/10.1002/anie.201702107openalex-snapshot
Enantioselective Heck–Matsuda Arylations through Chiral Anion Phase‐Transfer of Aryl Diazonium Salts
inferred← citeshttps://doi.org/10.1002/anie.202504012openalex-snapshot
Nitrate Reduction for Deaminative Suzuki–Miyaura Coupling of Anilines
inferred← citeshttps://doi.org/10.1002/aoc.2869openalex-snapshot
Palladium‐catalyzed Suzuki–Miyaura coupling with aryl and heteroaryl bromides using N,N,N′,N′‐tetra(diphenylphosphinomethyl)‐1,2‐ethylenediamine
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.3346openalex-snapshot
Carboxymethylcellulose‐supported palladium nanoparticles generated in situ from palladium(II) carboxymethylcellulose as an efficient and reusable catalyst for ligand‐ and base‐free Heck–Matsuda and Suzuki–Miyaura couplings
inferred← citeshttps://doi.org/10.1002/aoc.4934openalex-snapshot
Well‐dispersed N‐heterocyclic carbene–palladium complex anchored onto poly(acrylic acid)/poly(vinyl alcohol) nanofibers: Novel, superior and ecofriendly nanocatalyst for the Suzuki–Miyaura cross‐coupling reaction
inferred← citeshttps://doi.org/10.1002/cctc.201500179openalex-snapshot
Palladium Nanoparticles Supported on Sulfonic Acid Functionalized Silica as Trifunctional Heterogeneous Catalysts for Heck and Suzuki Reactions
inferred← citeshttps://doi.org/10.1002/cctc.202500267openalex-snapshot
A Well‐Defined Pd‐NHC Pre‐Catalyst for the Borylation of Aryl Chlorides
inferred← citeshttps://doi.org/10.1002/chem.200400928openalex-snapshot
Diaminocarbene‐ and Fischer‐Carbene Complexes of Palladium and Nickel by Oxidative Insertion: Preparation, Structure, and Catalytic Activity
inferred← citeshttps://doi.org/10.1002/chem.201001009openalex-snapshot
Polyoxometalate‐Based N‐Heterocyclic Carbene (NHC) Complexes for Palladium‐Mediated CC Coupling and Chloroaryl Dehalogenation Catalysis
inferred← citeshttps://doi.org/10.1002/chem.201300858openalex-snapshot
Chelation‐Assisted Cross‐Coupling of Anilines through In Situ Activation as Diazonium Salts with Boronic Acids under Ligand‐, Base‐, and Salt‐Free Conditions
inferred← citeshttps://doi.org/10.1002/chem.201603626openalex-snapshot
Using Anilines as Masked Cross‐Coupling Partners: Design of a Telescoped Three‐Step Flow Diazotization, Iododediazotization, Cross‐Coupling Process
inferred← citeshttps://doi.org/10.1002/chin.200213069openalex-snapshot
ChemInform Abstract: Palladium—Imidazolium Carbene Catalyzed Aryl, Vinyl, and Alkyl Suzuki—Miyaura Cross Coupling.
inferred← citeshttps://doi.org/10.1002/cjoc.201190063openalex-snapshot
Ligand‐free Suzuki‐Miyaura Cross‐Coupling Reactions of Aryltriazenes with Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/ejic.200400637openalex-snapshot
Ionic Liquids as Reaction Media for Palladium‐Catalysed Cross‐Coupling of Aryldiazonium Tetrafluoroborates with Potassium Organotrifluoroborates
inferred← citeshttps://doi.org/10.1002/ejoc.200300294openalex-snapshot
Potassium Trifluoro(organo)borates: New Perspectives in Organic Chemistry
inferred← citeshttps://doi.org/10.1002/ejoc.200600600openalex-snapshot
Recoverable Homogeneous Palladium(0) Catalyst for Cross‐Coupling Reactions of Arenediazonium Salts with Potassium Organotrifluoroborates: Detection of Catalytic Intermediates by Electrospray Ionization Mass Spectrometry
inferred← citeshttps://doi.org/10.1002/ejoc.201001620openalex-snapshot
Evolution and Synthetic Applications of the Heck–Matsuda Reaction: The Return of Arenediazonium Salts to Prominence
inferred← citeshttps://doi.org/10.1002/ejoc.201900622openalex-snapshot
Renaissance of 1,2,5‐Oxadiazolyl Diazonium Salts: Synthesis and Reactivity
inferred← citeshttps://doi.org/10.1002/ijch.201100018openalex-snapshot
Hybrid Polyoxometalates: Merging Organic and Inorganic Domains for Enhanced Catalysis and Energy Applications
inferred← citeshttps://doi.org/10.1007/978-3-540-36930-1_3openalex-snapshot
Palladium-catalyzed Reactions Using NHC Ligands
inferred← citeshttps://doi.org/10.1007/s10562-013-1126-zopenalex-snapshot
N-Heterocyclic Carbene Conjugated with Poly(ethylene glycol) for Palladium-Catalyzed Suzuki–Miyaura Coupling in Aqueous Solvents
inferred← citeshttps://doi.org/10.1007/s10847-016-0673-5openalex-snapshot
Pillar[5]arene-based N-heterocyclic carbene ligand for Pd-catalysed Suzuki reaction
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/s11172-006-0366-0openalex-snapshot
Reductive activation of arenes
inferred← citeshttps://doi.org/10.1016/b0-08-043748-6/09089-7openalex-snapshot
Metal Complexes as Catalysts for CC Cross-coupling Reactions
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00006-4openalex-snapshot
One or More CC Bond(s) Formed by Substitution: Substitution of Carbon–Nitrogen, –Phosphorus, –Arsenic, –Antimony, –Boron, –Silicon, –Germanium, and –Metal Functions
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00011-8openalex-snapshot
One or More CC Bond(s) Formed by Substitution or Addition
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00143-6openalex-snapshot
C–C Bond Formation by Cross-coupling
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.03966-4openalex-snapshot
C–C Bond Formation by Cross-Coupling
inferred← citeshttps://doi.org/10.1016/b978-008044412-3/50006-3openalex-snapshot
The Suzuki-Miyaura reaction
inferred← citeshttps://doi.org/10.1016/j.apcata.2010.02.004openalex-snapshot
Palladium(0) nanoparticles formed in situ in the Suzuki–Miyaura reaction: The effect of a palladium(II) precursor
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.cclet.2010.12.048openalex-snapshot
Amide as an efficient ligand in the palladium-catalyzed Suzuki coupling reaction in water/ethanol under aerobic conditions
inferred← citeshttps://doi.org/10.1016/j.ccr.2004.02.011openalex-snapshot
Catalytic methods for the synthesis of stilbenes with an emphasis on their phytoalexins
inferred← citeshttps://doi.org/10.1016/j.jiec.2023.04.006openalex-snapshot
Air and moisture stable robust bio-polymeric palladium catalyzed C C bond formation and its application to the synthesis of fungicidal
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.03.029openalex-snapshot
Phosphine-free Suzuki cross-coupling reactions under ultrasound
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.10.030openalex-snapshot
Triarylantimony dicarboxylates as pseudo-halides for palladium-catalyzed cross-coupling reaction with arylboronic acids and triarylbismuthanes without any base
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.09.038openalex-snapshot
Novel triphenylarsinyl-functionalized N-heterocyclic carbene ligands in palladium-catalyzed C–C coupling reactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2016.08.017openalex-snapshot
Polystyrene-resin supported N-heterocyclic carbene-Pd(II) complex based on plant-derived theophylline: A reusable and effective catalyst for the Suzuki-Miyaura cross-coupling reaction of arenediazonium tetrafluoroborate salts with arylboronic acids
inferred← citeshttps://doi.org/10.1016/j.micromeso.2016.01.014openalex-snapshot
Supported palladium ions inside periodic mesoporous organosilica with ionic liquid framework (Pd@IL-PMO) as an efficient green catalyst for S-arylation coupling
inferred← citeshttps://doi.org/10.1016/j.molcata.2005.06.024openalex-snapshot
Heck, Suzuki and Kumada–Corriu cross-coupling reactions mediated by complexes based on the upper rim of diphosphinated calix[4]arenes
inferred← citeshttps://doi.org/10.1016/j.molcata.2009.01.011openalex-snapshot
PdII square planar complexes of the type [IL]2[PdX4] as catalyst precursors for the Suzuki–Miyaura cross-coupling reaction. The first in situ ESI-MS evidence of [(IL)xPd3] clusters formation
inferred← citeshttps://doi.org/10.1016/j.tet.2003.12.012openalex-snapshot
Mizoroki–Heck reaction, catalysis by nitrogen ligand Pd complexes and activation of aryl bromides
inferred← citeshttps://doi.org/10.1016/j.tet.2005.05.071openalex-snapshot
Palladium catalyzed Suzuki–Miyaura coupling with aryl chlorides using a bulky phenanthryl N-heterocyclic carbene ligand
inferred← citeshttps://doi.org/10.1016/j.tet.2007.04.016openalex-snapshot
Copper(I)-catalysed homo-coupling of aryldiazonium salts: synthesis of symmetrical biaryls
inferred← citeshttps://doi.org/10.1016/j.tet.2007.08.115openalex-snapshot
Suzuki–Miyaura cross-coupling reaction as the key step for the synthesis of some new 4′-aryl and alkyl substituted analogues of amodiaquine and amopyroquine
inferred← citeshttps://doi.org/10.1016/j.tet.2008.02.083openalex-snapshot
Air-stable Pd(II) catalysts with cryptand-22 ligand for convenient and efficient Suzuki cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2012.05.068openalex-snapshot
General and highly efficient fluorinated-N-heterocyclic carbene–based catalysts for the palladium-catalyzed Suzuki–Miyaura reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.06.006openalex-snapshot
N-Heterocyclic carbene–palladium complex on polystyrene resin surface as polymer-supported catalyst and its application in Suzuki cross-coupling reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.04.105openalex-snapshot
Amphiphilic polymer supported N-heterocyclic carbene palladium complex for Suzuki cross-coupling reaction in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.05.065openalex-snapshot
Synthesis of polyhydroxylated ester analogs of the stilbene resveratrol using decarbonylative Heck couplings
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.10.163openalex-snapshot
Suzuki-type cross-coupling reaction of pentavalent triarylantimony diacetates with arylboronic acids without a base
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.08.072openalex-snapshot
Synthesis of diarylmethane derivatives from Stille cross-coupling reactions of benzylic halides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.01.090openalex-snapshot
B-Alkyl Suzuki–Miyaura cross-coupling of tri-n-alkylboranes with arylbromides bearing acidic functions under mild non-aqueous conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.01.120openalex-snapshot
Synthesis of oxadiazole-2-oxide analogues as potential antischistosomal agents
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.11.099openalex-snapshot
A base-free, one-pot diazotization/cross-coupling of anilines with arylboronic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.11.053openalex-snapshot
Suzuki–Miyaura cross-coupling of aryldiazonium silica sulfates under mild and heterogeneous conditions
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.2013.11.027openalex-snapshot
Synthesis of novel chiral bidentate hydroxyalkyl-N-heterocyclic carbene ligands and their application in palladium-catalyzed Mizoroki–Heck couplings and asymmetric addition of diethylzinc to benzaldehyde
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.05.055openalex-snapshot
Metal-free efficient cross coupling of aromatic aldehydes with aryldiazonium tetrafluoroborates using DTBP as a radical initiator
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.06.045openalex-snapshot
Desulfinylative Pd-catalyzed coupling reaction of arenediazonium salt with aryl sulfinates to give unsymmetrical biaryls
inferred← citeshttps://doi.org/10.1016/s0022-328x(03)00476-5openalex-snapshot
Chiral diaminocarbene palladium(II) complexes: synthesis, reduction to Pd(0) and activity in the Mizoroki–Heck reaction as recyclable catalysts
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)02186-xopenalex-snapshot
Palladium–imidazolium-catalyzed carbonylative coupling of aryl diazonium ions and aryl boronic acids
inferred← citeshttps://doi.org/10.1016/s0040-4039(03)00023-6openalex-snapshot
Base-free oxidative homocoupling of arylboronic esters
inferred← citeshttps://doi.org/10.1016/s0040-4039(03)01131-6openalex-snapshot
Synthesis of resveratrol using a direct decarbonylative Heck approach from resorcylic acid
inferred← citeshttps://doi.org/10.1016/s0040-4039(03)01743-xopenalex-snapshot
Palladium-catalyzed Suzuki–Miyaura reaction using aminophosphine as ligand
inferred← citeshttps://doi.org/10.1016/s0959-6380(02)80010-1openalex-snapshot
Chapter 5.4 Five membered ring systems: With more than one N atom
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c04673openalex-snapshot
Three-Coordinate Monomeric Phosphido Complexes of Ni(II)
inferred← citeshttps://doi.org/10.1021/acscatal.0c01462openalex-snapshot
Suzuki–Miyaura Cross-Coupling of Sulfoxides
inferred← citeshttps://doi.org/10.1021/acscatal.7b00300openalex-snapshot
Modular Synthesis of Enantioenriched 1,1,2-Triarylethanes by an Enantioselective Arylboration and Cross-Coupling Sequence
inferred← citeshttps://doi.org/10.1021/cm030296iopenalex-snapshot
Liquid Crystals ofN,N‘-Dialkylimidazolium Salts Comprising Palladium(II) and Copper(II) Ions
inferred← citeshttps://doi.org/10.1021/cr0509861openalex-snapshot
Diazonium Salts as Substrates in Palladium-Catalyzed Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/cr1002276openalex-snapshot
Transmetalation of Unsaturated Carbon Nucleophiles from Boron-Containing Species to the Mid to Late d-Block Metals of Relevance to Catalytic C−X Coupling Reactions (X = C, F, N, O, Pb, S, Se, Te)
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/jo050016dopenalex-snapshot
A Tandem Heck-Carbocyclization/Suzuki-Coupling Approach to the Stereoselective Syntheses of Asymmetric 3,3-(Diarylmethylene)indolinones
inferred← citeshttps://doi.org/10.1021/jo050721mopenalex-snapshot
Polymer-Supported N-Heterocyclic Carbene−Palladium Complex for Heterogeneous Suzuki Cross-Coupling Reaction
inferred← citeshttps://doi.org/10.1021/jo201437jopenalex-snapshot
Hiyama Cross-Coupling of Arenediazonium Salts under Mild Reaction Conditions
inferred← citeshttps://doi.org/10.1021/jo500026gopenalex-snapshot
Palladium-Catalyzed Suzuki Cross-Coupling of Arylhydrazines via C–N Bond Cleavage
inferred← citeshttps://doi.org/10.1021/jo5023052openalex-snapshot
Computational Study of Metal Free Alcohol Dehydrogenation Employing Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1021/jo8016633openalex-snapshot
A Nonsymmetric Pincer-Catalyzed Suzuki−Miyaura Arylation of Benzyl Halides and Other Nonactivated Unusual Coupling Partners
inferred← citeshttps://doi.org/10.1021/ol0171463openalex-snapshot
Microwave-Assisted Synthesis of Pinacol Boronates from Aryl Chlorides Catalyzed by a Palladium/Imidazolium Salt System
inferred← citeshttps://doi.org/10.1021/ol035147kopenalex-snapshot
Sonogashira Coupling Using Bulky Palladium-Phenanthryl Imidazolium Carbene Catalysis
inferred← citeshttps://doi.org/10.1021/ol036436bopenalex-snapshot
Boron Trifluoride Induced Palladium-Catalyzed Cross-Coupling Reaction of 1-Aryltriazenes with Areneboronic Acids
inferred← citeshttps://doi.org/10.1021/om0498044openalex-snapshot
1,4-Addition of Arylboronic Acids and Arylsiloxanes to α,β-Unsaturated Carbonyl Compounds via Transmetalation to Dicationic Palladium(II) Complexes
inferred← citeshttps://doi.org/10.1021/om050678topenalex-snapshot
Enantioselective 1,4-Addition of Ar3Bi, [ArBF3]K, and ArSiF3 to Enones Catalyzed by a Dicationic Palladium(II)−Chiraphos or −Dipamp Complex
inferred← citeshttps://doi.org/10.1021/om800832ropenalex-snapshot
γ-Selective Cross-Coupling Reactions of Potassium Allyltrifluoroborates with Haloarenes Catalyzed by a Pd(0)/D-t-BPF or Pd(0)/Josiphos ((R,S)-CyPF-t-Bu) Complex: Mechanistic Studies on Transmetalation and Enantioselection
inferred← citeshttps://doi.org/10.1021/op500299topenalex-snapshot
Using Aryl Diazonium Salts in Palladium-Catalyzed Reactions under Safer Conditions
inferred← citeshttps://doi.org/10.1039/b109666bopenalex-snapshot
20 Organometallic chemistry of monometallic species
inferred← citeshttps://doi.org/10.1039/c0cc03781hopenalex-snapshot
Iron-catalyzed synthesis of glycine derivatives via carbon–nitrogen bond cleavage using diazoacetate
inferred← citeshttps://doi.org/10.1039/c1ob06752dopenalex-snapshot
Suzuki–Miyaura cross-couplings of arenediazonium tetrafluoroborate salts with arylboronic acids catalyzed by aluminium hydroxide-supported palladium nanoparticles
inferred← citeshttps://doi.org/10.1039/c2gc15679bopenalex-snapshot
Suzuki-Miyaura cross-coupling of arenediazonium salts catalyzed by alginate/gellan-stabilized palladium nanoparticles under aerobic conditions in water
inferred← citeshttps://doi.org/10.1039/c3ob27366kopenalex-snapshot
Recent applications of arene diazonium salts in organic synthesis
inferred← citeshttps://doi.org/10.1039/c3ra44620dopenalex-snapshot
Graphene oxide supported N-heterocyclic carbene-palladium as a novel catalyst for the Suzuki–Miyaura reaction
inferred← citeshttps://doi.org/10.1039/c4ob01286kopenalex-snapshot
Removal of amino groups from anilines through diazonium salt-based reactions
inferred← citeshttps://doi.org/10.1039/c4ob01430hopenalex-snapshot
Enantioselective copper catalysed C–H insertion reaction of 2-sulfonyl-2-diazoacetamides to form γ-lactams
inferred← citeshttps://doi.org/10.1039/c4ra07455fopenalex-snapshot
Palladium-catalyzed desulfitative cross-coupling of arylsulfinates with arylboronic acids
inferred← citeshttps://doi.org/10.1039/c5gc02314aopenalex-snapshot
Ligand-free Pd catalyzed cross-coupling reactions in an aqueous hydrotropic medium
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/c5ra10291jopenalex-snapshot
Copper catalyzed synthesis of unsymmetrical diaryl sulfones from an arenediazonium salt and sodium p-toluenesulfinate
inferred← citeshttps://doi.org/10.1039/c5ra15875copenalex-snapshot
Cross-coupling reaction of aryl diazonium salts with azodicarboxylate using FeCl 2
inferred← citeshttps://doi.org/10.1039/c6cc03105fopenalex-snapshot
Arenediazonium salts as electrophiles for the oxidative addition of gold( i )
inferred← citeshttps://doi.org/10.1039/c6nj01717gopenalex-snapshot
The promoting effect of pyridine ligands in the Pd-catalysed Heck–Matsuda reaction
inferred← citeshttps://doi.org/10.1039/c6qo00530fopenalex-snapshot
Reductive insertion of sulfur dioxide for the synthesis of trifluoromethyl thiolsulphonates through a one-pot reaction of aniline and trifluoromethanesulfanylamide
inferred← citeshttps://doi.org/10.1039/c6ra12557copenalex-snapshot
Aryl diazonium salt and thioacetamide: a catalyst free, efficient blend of an inexpensive arylating agent with “S” surrogate for sulphide synthesis
inferred← citeshttps://doi.org/10.1039/c7cc07543jopenalex-snapshot
Palladium-catalyzed denitrogenative functionalizations of benzotriazoles with alkenes and 1,3-dienes
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/c8ob00591eopenalex-snapshot
Aromatic substitutions of arenediazonium salts via metal catalysis, single electron transfer, and weak base mediation
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/10.1039/d4ra07556kopenalex-snapshot
Advances in pyrazolo[1,5- a ]pyrimidines: synthesis and their role as protein kinase inhibitors in cancer treatment
inferred← citeshttps://doi.org/10.1246/bcsj.81.1535openalex-snapshot
Metal-Catalyzed Reactions of Organoboronic Acids and Esters
inferred← citeshttps://doi.org/10.24820/ark.5550190.p011.559openalex-snapshot
Sonogashira coupling of arenediazonium salts: discovery and developments
inferred← citeshttps://doi.org/10.3762/bjoc.6.70openalex-snapshot
Suzuki–Miyaura cross-coupling reaction of 1-aryltriazenes with arylboronic acids catalyzed by a recyclable polymer-supported N-heterocyclic carbene–palladium complex catalyst
inferred← citeshttps://doi.org/10.3987/rev-09-662-1openalex-snapshot
Recent Development in Palladium-Mediated Synthesis of Oxygen Heterocycles
inferred← citeshttps://doi.org/10.3987/rev-09-662-2openalex-snapshot
Recent Development in Palladium-Mediated Synthesis of Nitrogen Heterocycles
inferred← citeshttps://doi.org/10.70675/327bf767z083cz4c40z8458zb7d3f964700aopenalex-snapshot
Synthesis of polymers containing perfluoroalkyl sulfonated side chains for proton conductivity membranes
inferred← citeshttps://doi.org/10.70675/3c42256ez961bz43c1z8a6bza7a04599322bopenalex-snapshot
Réactions photorédox appliquées à la valorisation du monoxyde de carbone et du 1,3-butadiène
inferred← citeshttps://doi.org/10.70675/6f251c39zce64z4ea6z8194zfcbb1226d97fopenalex-snapshot
Nouvelles méthodes de synthèse pour la formation de liaisons C(aryl)-hétéroatome et C(aryl)-C par réactions de substitution nucléophile aromatique et vinylique
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