On the public citation graph

Catalytic Suzuki Coupling Reactions by Amido Phosphine Complexes of Palladium

0 signed · 105 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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/anie.199518491openalex-snapshot
Carbenoid or Lithium Complex of a Carbanion? Synthesis and Structure of (Me3Si)2CP(aryl)C(Cl)Li(thf)3 and LiCl Elimination To Give the Phosphirene
inferredcites →https://doi.org/10.1002/anie.200353615openalex-snapshot
A Rationally Designed Universal Catalyst for Suzuki–Miyaura Coupling Processes
inferredcites →https://doi.org/10.1016/j.tetlet.2004.05.144openalex-snapshot
Iminophosphine–palladium(0) complexes as highly active catalysts in the Suzuki reaction. Synthesis of undecaaryl substituted corroles
inferredcites →https://doi.org/10.1016/s0022-1139(01)00463-8openalex-snapshot
Synthesis and comparison of N-fluorobis[(perfluoroalkyl)sulfonyl]imides with different perfluoroalkyl groups
inferredcites →https://doi.org/10.1016/s0022-328x(97)00736-5openalex-snapshot
Chelating N-heterocyclic carbene ligands in palladium-catalyzed heck-type reactions
inferredcites →https://doi.org/10.1016/s0022-328x(99)00237-5openalex-snapshot
Combining N-heterocyclic carbenes and phosphines: improved palladium(II) catalysts for aryl coupling reactions
inferredcites →https://doi.org/10.1016/s0040-4020(97)10010-2openalex-snapshot
Investigations into ambient temperature biaryl coupling reactions
inferredcites →https://doi.org/10.1016/s0040-4039(01)01301-6openalex-snapshot
Suzuki cross-coupling of arylboronic acids mediated by a hydrosoluble Pd(0)/TPPTS catalyst
inferredcites →https://doi.org/10.1021/cr960118ropenalex-snapshot
Cyclometalated Phosphine-Based Pincer Complexes: Mechanistic Insight in Catalysis, Coordination, and Bond Activation
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/ja00402a067openalex-snapshot
Hybrid multidentate ligands. Tridentate amidophosphine complexes of nickel(II) and palladium(II)
inferredcites →https://doi.org/10.1021/ja038631ropenalex-snapshot
A General Method for the Suzuki−Miyaura Cross-Coupling of Sterically Hindered Aryl Chlorides: Synthesis of Di- and Tri-ortho-substituted Biaryls in 2-Propanol at Room Temperature
inferredcites →https://doi.org/10.1021/ja9729692openalex-snapshot
Highly Active Pd(II) PCP-Type Catalysts for the Heck Reaction
inferredcites →https://doi.org/10.1021/ja992130hopenalex-snapshot
Highly Active Palladium Catalysts for Suzuki Coupling Reactions
inferredcites →https://doi.org/10.1021/ol0341849openalex-snapshot
Di-2-pyridylmethylamine-Based Palladium Complexes as New Catalysts for Heck, Suzuki, and Sonogashira Reactions in Organic and Aqueous Solvents
inferredcites →https://doi.org/10.1081/scc-100108234openalex-snapshot
EASY LARGE-SCALE SYNTHESIS OF STERICALLY ENCUMBERED 2-IODOBIPHENYLS AND SOME DERIVATIVES THEREOF

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/10.1002/047084289x.rn00684openalex-snapshot
Tricyclohexylphosphine
inferred← citeshttps://doi.org/10.1002/047084289x.rn00684.pub2openalex-snapshot
Tricyclohexylphosphine
inferred← citeshttps://doi.org/10.1002/9781118662083.cot01-002openalex-snapshot
Formation of Alkanes and Arenes by Coupling Reactions
inferred← citeshttps://doi.org/10.1002/adsc.200505473openalex-snapshot
On the Nature of the Active Species in Palladium Catalyzed Mizoroki–Heck and Suzuki–Miyaura Couplings – Homogeneous or Heterogeneous Catalysis, A Critical Review
inferred← citeshttps://doi.org/10.1002/aoc.1713openalex-snapshot
Highly efficient orthopalladated complexes of second and third benzyl amine for catalyzing the Suzuki cross‐coupling reaction
inferred← citeshttps://doi.org/10.1002/aoc.1755openalex-snapshot
Highly efficient amine‐based catalytic system for room temperature Suzuki–Miyaura reactions of aryl halides with arylboronic acids
inferred← citeshttps://doi.org/10.1002/aoc.1801openalex-snapshot
Iron(0), rhodium(I) and palladium(II) complexes with p‐(N,N‐dimethylaminophenyl) diphenylphosphine and the application of the palladium complex as a catalyst for the Suzuki–Miyaura cross‐coupling reaction
inferred← citeshttps://doi.org/10.1002/aoc.2852openalex-snapshot
A comparative Suzuki reaction of aryl halides using a new dimeric orthopalladated complex under conventional and microwave irradiation conditions
inferred← citeshttps://doi.org/10.1002/aoc.6128openalex-snapshot
Amido PNP pincer complexes of palladium(II) and platinum(II): Synthesis, structure, and reactivity
inferred← citeshttps://doi.org/10.1002/cctc.201000260openalex-snapshot
The Heck Reaction of Allylic Alcohols Catalyzed by Palladium Nanoparticles in Water: Chemoenzymatic Synthesis of ( R )‐(−)‐Rhododendrol
inferred← citeshttps://doi.org/10.1002/chem.200701418openalex-snapshot
Insights into Sonogashira Cross‐Coupling by High‐Throughput Kinetics and Descriptor Modeling
inferred← citeshttps://doi.org/10.1002/chem.201406486openalex-snapshot
Chemistry of Stannylene‐Based Lewis Pairs: Dynamic Tin Coordination Switching Between Donor and Acceptor Character
inferred← citeshttps://doi.org/10.1002/chin.200526054openalex-snapshot
Catalytic Suzuki Coupling Reactions by Amido Phosphine Complexes of Palladium.
inferred← citeshttps://doi.org/10.1002/cssc.202501205openalex-snapshot
Durable Heterogeneous Pd‐PNP Pincer Complex for CarbonCarbon Bond Formation in Continuous‐Flow Systems
inferred← citeshttps://doi.org/10.1002/ejic.201001362openalex-snapshot
Synthesis, Structure, and Ring‐Opening Polymerization Catalysis of Zinc Complexes Containing Amido Phosphinimine Ligands
inferred← citeshttps://doi.org/10.1002/ejic.201100952openalex-snapshot
Synthesis and Structural Characterization of Zinc Complexes that Contain Chelating Phenolate Phosphane Ligands
inferred← citeshttps://doi.org/10.1002/ejic.201101434openalex-snapshot
Nucleophilic Attack on Coordinated Imines: The Synthesis of C‐Bonded Acetylacetonates of Palladium(II) and Mechanistic Insights
inferred← citeshttps://doi.org/10.1002/ejoc.201200355openalex-snapshot
An Efficient Class of P,N‐Type “PhMezole‐phos” Ligands: Applications in Palladium‐Catalyzed Suzuki Coupling of Aryl Chlorides
inferred← citeshttps://doi.org/10.1002/ejoc.201402699openalex-snapshot
A Versatile and Efficient Palladium– meta ‐Terarylphosphine Catalyst for the Copper‐Free Sonogashira Coupling of (Hetero‐)Aryl Chlorides and Alkynes
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/zaac.201300107openalex-snapshot
Rhodium(III), Palladium(II) and Rhenium(I) Complexes with 7‐(Diphenylphosphine)‐indole and ‐indolate
inferred← citeshttps://doi.org/10.1007/978-4-431-54604-7_8openalex-snapshot
Applications of Five-Membered Ring Products as Catalysts in Cyclometalation Reactions
inferred← citeshttps://doi.org/10.1007/s10562-013-0979-5openalex-snapshot
Nickel-catalyzed C(sp2)–C(sp2) Cross Coupling Reactions of Sulfur-Functionalities and Grignard Reagents
inferred← citeshttps://doi.org/10.1016/j.apcata.2013.01.021openalex-snapshot
Silica-supported PEI capped nanopalladium as potential catalyst in Suzuki, Heck and Sonogashira coupling reactions
inferred← citeshttps://doi.org/10.1016/j.cclet.2009.03.034openalex-snapshot
Synthesis of substituted polyaryls via sterically hindered double Suzuki cross-couplings
inferred← citeshttps://doi.org/10.1016/j.ccr.2006.01.001openalex-snapshot
Metal complexes of chelating diarylamido phosphine ligands
inferred← citeshttps://doi.org/10.1016/j.crci.2013.05.019openalex-snapshot
Seven-membered Pd(II) complexes containing symmetric phosphorus ylides: Synthesis, characterization and high catalytic activity toward Suzuki cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.05.074openalex-snapshot
Inhibition of 17β-HSD1: SAR of bicyclic substituted hydroxyphenylmethanones and discovery of new potent inhibitors with thioether linker
inferred← citeshttps://doi.org/10.1016/j.ica.2006.07.050openalex-snapshot
Preparation and structural characterization of group 1 metal complexes containing a chelating biphenolato phosphine ligand
inferred← citeshttps://doi.org/10.1016/j.ica.2018.06.013openalex-snapshot
Palladium(II) catalyzed Suzuki C C coupling reactions with imino- and amino-phosphine ligands
inferred← citeshttps://doi.org/10.1016/j.inoche.2013.08.010openalex-snapshot
New dimeric phosphine ylide copper (I) complexes: Synthesis, coordination behavior, and application in Suzuki cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.02.036openalex-snapshot
Three types of reactions with intramolecular five-membered ring compounds in organic synthesis
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.05.046openalex-snapshot
Synthesis and application of novel ionic phosphine ligands with a cobaltocenium backbone
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.07.022openalex-snapshot
Rare earth metal bis(alkyl) complexes bearing amino phosphine ligands: Synthesis and catalytic activity toward ethylene polymerization
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2009.02.019openalex-snapshot
Phosphine free diamino-diol based palladium catalysts and their application in Suzuki–Miyaura cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2012.10.004openalex-snapshot
Four-coordinate Pd(II) complexes containing non-symmetric phosphorus ylides: Synthesis, characterization, and catalytic behavior towards Suzuki reaction
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2015.12.032openalex-snapshot
Catalytic Suzuki couplings by an amido pincer complex of palladium
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2018.05.015openalex-snapshot
Applications of cyclometalation reaction five-membered ring products
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.mencom.2013.11.014openalex-snapshot
Catalytic activity of k3-X,N,Y-palladium pincer complexes (X, Y = O, S) with (thio)phosphoryl-substituted carbamoylmethylphosphine oxide and sulfide ligands in the Suzuki cross-coupling
inferred← citeshttps://doi.org/10.1016/j.poly.2014.06.010openalex-snapshot
Palladium and platinum complexes of the new ligands containing P–N and P–O bonds
inferred← citeshttps://doi.org/10.1016/j.poly.2016.05.046openalex-snapshot
A new Pd(II) complex of a sulfur ylide; Synthesis, X-ray characterization, theoretical study and catalytic activity toward the Suzuki–Miyaura reaction
inferred← citeshttps://doi.org/10.1016/j.poly.2016.11.006openalex-snapshot
Titanium, hafnium, and tantalum complexes of a potentially triphenolate phosphine ligand that is unexpectedly prone to O-protonation
inferred← citeshttps://doi.org/10.1016/j.reactfunctpolym.2011.07.006openalex-snapshot
Active immobilized palladium catalyst based on multiporous amphiphilic graft copolymer
inferred← citeshttps://doi.org/10.1016/j.tet.2007.04.057openalex-snapshot
Efficient palladium-catalyzed Suzuki–Miyaura coupling of aryl chlorides with arylboronic acids using benzoferrocenyl phosphines as supporting ligands
inferred← citeshttps://doi.org/10.1016/j.tet.2007.10.081openalex-snapshot
An inexpensive and highly stable ligand 1,4-bis(2-hydroxy-3,5-di-tert-butylbenzyl)piperazine for Mizoroki–Heck and room temperature Suzuki–Miyaura cross-coupling reactions
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.2011.03.066openalex-snapshot
Probing the electronic demands of transmetalation in the palladium-catalyzed cross-coupling of arylsilanolates
inferred← citeshttps://doi.org/10.1016/j.tet.2012.10.055openalex-snapshot
Benzimidazole-based palladium–N-heterocyclic carbene: a useful catalyst for C–C cross-coupling reaction at ambient condition
inferred← citeshttps://doi.org/10.1016/j.tet.2014.02.011openalex-snapshot
Calculated linear free energy relationships in the course of the Suzuki–Miyaura coupling reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.05.017openalex-snapshot
P,N-Type benzimidazolyl phosphine ligands for the palladium-catalyzed Suzuki coupling of potassium aryltrifluoroborates and aryl chlorides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.03.115openalex-snapshot
A highly efficient Schiff-base derived palladium catalyst for the Suzuki–Miyaura reactions of aryl chlorides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.12.071openalex-snapshot
Highly active palladium catalysts containing a 1,10-phenanthroline analogue N-heterocyclic carbene for room temperature Suzuki-Miyaura coupling reactions of aryl chlorides with arylboronic acids in aqueous media
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.5b02208openalex-snapshot
Homo- and Heteropolynuclear Clusters of Phosphine Triphenolates
inferred← citeshttps://doi.org/10.1021/ar600003hopenalex-snapshot
Metal Unsaturation and Ligand Hemilability in Suzuki Coupling
inferred← citeshttps://doi.org/10.1021/ic050599+openalex-snapshot
Zirconium and Hafnium Complexes Containing Bidentate Diarylamido−Phosphine Ligands
inferred← citeshttps://doi.org/10.1021/ic101883uopenalex-snapshot
Comparison of Structure and Reactivity of Phosphine-Amido and Hemilabile Phosphine-Amine Chelates of Rhodium
inferred← citeshttps://doi.org/10.1021/ic102194zopenalex-snapshot
Group 4 Complexes of atert-Butylphosphine-Bridged Biphenolate Ligand
inferred← citeshttps://doi.org/10.1021/ic702293dopenalex-snapshot
Fluorinated Diarylamido Complexes of Lithium, Zirconium, and Hafnium
inferred← citeshttps://doi.org/10.1021/ic802125zopenalex-snapshot
Biphenolate Phosphine Complexes of Tantalum
inferred← citeshttps://doi.org/10.1021/ic802286uopenalex-snapshot
Palladium N(CH2CH2PiPr2)2-Dialkylamides: Synthesis, Structural Characterization, and Reactivity
inferred← citeshttps://doi.org/10.1021/ja065505popenalex-snapshot
Intermolecular Arene C−H Activation by Nickel(II)
inferred← citeshttps://doi.org/10.1021/jo900550gopenalex-snapshot
Biphenylene-Substituted Ruthenocenylphosphine for Suzuki−Miyaura Coupling of Sterically Hindered Aryl Bromides
inferred← citeshttps://doi.org/10.1021/om201041zopenalex-snapshot
Divergent Carbonylation Reactivity Preferences of Nickel Complexes Containing Amido Pincer Ligands: Migratory Insertion versus Reductive Elimination
inferred← citeshttps://doi.org/10.1021/om5006353openalex-snapshot
Nickel(II) Complexes Containing Bidentate Diarylamido Phosphine Chelates: Kumada Couplings Kinetically Preferred to β-Hydrogen Elimination
inferred← citeshttps://doi.org/10.1021/om701294aopenalex-snapshot
Phosphorus and Olefin Substituent Effects on the Insertion Chemistry of Nickel(II) Hydride Complexes Containing Amido Diphosphine Ligands
inferred← citeshttps://doi.org/10.1021/om800175aopenalex-snapshot
A Nonsymmetric Pincer-Type Palladium Catalyst In Suzuki, Sonogashira, and Hiyama Couplings in Neat Water
inferred← citeshttps://doi.org/10.1021/om800251sopenalex-snapshot
Two Competing Mechanisms for the Copper-Free Sonogashira Cross-Coupling Reaction
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/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/10.1039/b501520kopenalex-snapshot
Benzene C–H activation by platinum(ii) complexes of bis(2-diphenylphosphinophenyl)amide
inferred← citeshttps://doi.org/10.1039/b503101jopenalex-snapshot
Pentafluorophenyl imidato palladium(ii) complexes: catalysts for Suzuki cross-coupling reactions
inferred← citeshttps://doi.org/10.1039/b701517hopenalex-snapshot
Aryl bromide/triflate selectivities reveal mechanistic divergence in palladium-catalysed couplings; the Suzuki–Miyaura anomaly
inferred← citeshttps://doi.org/10.1039/b915184bopenalex-snapshot
Suzuki-Miyaura cross-coupling catalyzed by protein-stabilized palladium nanoparticles under aerobic conditions in water: application to a one-pot chemoenzymatic enantioselective synthesis of chiral biaryl alcohols
inferred← citeshttps://doi.org/10.1039/c2cc15972dopenalex-snapshot
An efficient palladium–benzimidazolyl phosphine complex for the Suzuki–Miyaura coupling of aryl mesylates: facile ligand synthesis and metal complex characterization
inferred← citeshttps://doi.org/10.1039/c3qi00086aopenalex-snapshot
Catalytic Sonogashira couplings mediated by an amido pincer complex of palladium
inferred← citeshttps://doi.org/10.1039/c4ra11186aopenalex-snapshot
Phosphine-stabilized Pd nanoparticles supported on silica as a highly active catalyst for the Suzuki–Miyaura cross-coupling reaction
inferred← citeshttps://doi.org/10.1039/c5ob00289copenalex-snapshot
Dendrimer-encapsulated Pd nanoparticles as catalysts for C–C cross-couplings in flow microreactors
inferred← citeshttps://doi.org/10.1039/c6dt02143copenalex-snapshot
Aluminum complexes containing biphenolate phosphine ligands: synthesis and living ring-opening polymerization catalysis
inferred← citeshttps://doi.org/10.1039/c6sc02118bopenalex-snapshot
Site-selective Suzuki–Miyaura coupling of heteroaryl halides – understanding the trends for pharmaceutically important classes
inferred← citeshttps://doi.org/10.1039/d2ra05230jopenalex-snapshot
Aqueous Suzuki couplings mediated by a hydrophobic catalyst
inferred← citeshttps://doi.org/10.1080/00958972.2012.759216openalex-snapshot
Five-membered cyclopalladated complex containing bidentate phosphine ligands; Synthesis, characterization, and highly efficient Suzuki cross-coupling reactions
inferred← citeshttps://doi.org/10.31237/osf.io/udw5kopenalex-snapshot
Activation of diboron reagents: The development of mild conditions for the synthesis of unique organoboron compounds
inferred← citeshttps://doi.org/10.3184/174751913x13662179283121openalex-snapshot
PdCl 2 (1-methylimidazole) 2 -catalysed Suzuki–Miyaura and Mizoroki–Heck Reactions Performed in Neat Water
inferred← citeshttps://doi.org/10.3389/fchem.2018.00607openalex-snapshot
Enhanced Reactivity of Aluminum Complexes Containing P-Bridged Biphenolate Ligands in Ring-Opening Polymerization Catalysis
inferred← citeshttps://doi.org/10.4236/mrc.2016.53006openalex-snapshot
Applications of Cyclometalation Five-Membered Ring Products and Intermediates as Catalytic Agents
inferred← citeshttps://doi.org/10.70675/d08da350z1c84z4fa6zadc6z2c727384541eopenalex-snapshot
Influence of the polymer network properties on the in situ synthesis of palladium nanoparticles : application to catalytic membranes of high efficiency in fine chemistry
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.