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Highly Active Pd(II) PCP-Type Catalysts for the Heck Reaction
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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.199518481openalex-snapshot
Palladacycles as Efficient Catalysts for Aryl Coupling Reactions
inferredcites →https://doi.org/10.1002/anie.199523741openalex-snapshot
Self‐Assembly of Polyanions at a Metal Cation Template: Syntheses and Structures of [{Ag([18]aneS6)}I7]n and [Ag([18]aneS6)]I3
inferredcites →https://doi.org/10.1002/anie.199623591openalex-snapshot
A Route to Pdo from PdII Metallacycles in Animation and Cross‐Coupling Chemistry
inferredcites →https://doi.org/10.1002/cber.19961291018openalex-snapshot
Palladium‐Catalyzed Reactions in Industry, 4[]. Synthesis of New Palladium Catalysts: First Isolation and Characterization of all Intermediates in a Cyclopalladation Reaction
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Facile catalytic coupling of aryl bromides with terminal alkynes by phospha-palladacycles
inferredcites →https://doi.org/10.1021/om00042a008openalex-snapshot
Palladium-catalyzed vinylation of aryl chlorides. Chelate effect in catalysis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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The Structure-Property Correlation in Homocoupling Reaction; a Case Study by Clamshell and Planar Palladium Complexes
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13C NMR of Pd-aryl complexes. Chemical shifts and Pd π-back-bonding
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Fast Palladium Catalyzed Arylation of Alkenes Using Bulky Monodentate Phosphorus Ligands
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Design neuartiger Hexametall-Wagenradmoleküle aus persubstituierten Benzolverbindungen
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Hydrogen-Transfer Catalysis with Pincer-Aryl Ruthenium(II) Complexes
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[2,6-Bis[(bis(1-methylethyl)phosphino-P]methyl]-3,5 dimethylphenyl]methyl-C]tri-fluoroacetato-O)palladium
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Structural Investigation in Solution of a Series of Five-Coordinate Bisphosphanylaryl Ruthenium(II) Complexes
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Computational Study of a New Heck Reaction Mechanism Catalyzed by Palladium(II/IV) Species
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Highly Efficient Phosphapalladacyclic Catalysts for the Hydroarylation of Norbornene
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inferred← citeshttps://doi.org/10.1002/adsc.200404161openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.200404270openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200803953openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/slct.201801185openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/3-540-68525-1_8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10562-005-5869-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11244-006-0008-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11244-006-0119-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12039-015-0958-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00011-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00103-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00179-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-822091-7.00003-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-822091-7.00005-1openalex-snapshot
An outlook on the applications of pincer-metal complexes in catalytic dehydrogenation chemistry
inferred← citeshttps://doi.org/10.1016/b978-044453138-4/50002-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-044453138-4/50010-6openalex-snapshot
The chemistry of PCP pincer phosphinite transition metal complexes
inferred← citeshttps://doi.org/10.1016/b978-044453138-4/50013-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-044453138-4/50018-0openalex-snapshot
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Recent progress on group 10 metal complexes of pincer ligands: From synthesis to activities and catalysis
inferred← citeshttps://doi.org/10.1016/bs.adomc.2024.04.002openalex-snapshot
A tale of two metals: The Mizoroki-Heck reaction as a guide to compare the chemical characters of nickel and palladium in catalysis
inferred← citeshttps://doi.org/10.1016/j.cattod.2007.10.043openalex-snapshot
PdCl2(bipy) complex—An efficient catalyst for Heck reaction in glycol–organic biphasic medium
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Monodentate phosphorus-coordinated palladium(II) complexes as new catalyst for Mizoroki-Heck reaction of aryl halides with electron-deficient olefins
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Pyridylthioethers: a promising class of polydentate ligands in palladium and platinum coordination
inferred← citeshttps://doi.org/10.1016/j.ccr.2004.05.011openalex-snapshot
Intramolecular five-membered ring compounds and their applications
inferred← citeshttps://doi.org/10.1016/j.ccr.2004.06.012openalex-snapshot
The development of palladium catalysts for CC and Cheteroatom bond forming reactions of aryl chloride substrates
inferred← citeshttps://doi.org/10.1016/j.ccr.2005.02.001openalex-snapshot
Structural and mechanistic studies of Pd-catalyzed CC bond formation: The case of carbonylation and Heck reaction
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.ccr.2006.11.013openalex-snapshot
Monomolecular, nanosized and heterogenized palladium catalysts for the Heck reaction
inferred← citeshttps://doi.org/10.1016/j.ccr.2008.02.002openalex-snapshot
Cycloheptatrienyl, alkyl and aryl PCP-pincer complexes: Ligand backbone effects and metal reactivity
inferred← citeshttps://doi.org/10.1016/j.ccr.2019.01.008openalex-snapshot
The role of palladium nanoparticles in catalytic C–C cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.ccr.2020.213203openalex-snapshot
Cyclopalladated complexes containing an (sp3)C–Pd bond
inferred← citeshttps://doi.org/10.1016/j.ccr.2022.214915openalex-snapshot
Transition metal pincer complexes: A series of potential catalysts in C H activation reactions
inferred← citeshttps://doi.org/10.1016/j.ccr.2026.218584openalex-snapshot
Palladium complexes of pincer-structured organosulfur ligands: coordination features, reactivity, and applications
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e17608openalex-snapshot
Palladium complexes containing NNN pincer type ligands and their activities in Suzuki-Miyaura cross coupling reaction
inferred← citeshttps://doi.org/10.1016/j.ica.2003.11.014openalex-snapshot
sp3 C–H and sp2 C–H agostic ruthenium complexes: a combined experimental and theoretical study
inferred← citeshttps://doi.org/10.1016/j.ica.2004.06.002openalex-snapshot
Nickel promoted C–H, C–C and C–O bond activation in solution
inferred← citeshttps://doi.org/10.1016/j.ica.2005.07.050openalex-snapshot
Ruthenium PCP–bis(phosphinite) pincer complexes
inferred← citeshttps://doi.org/10.1016/j.ica.2005.09.016openalex-snapshot
Catalytic hydroxylation of 1-propanol by platinum NCN and PCP pincer complexes using CuCl2 as oxidant
inferred← citeshttps://doi.org/10.1016/j.ica.2005.09.030openalex-snapshot
Synthesis and characterization of electronically varied XCX palladacycles with functional arene groups
inferred← citeshttps://doi.org/10.1016/j.ica.2006.07.092openalex-snapshot
Synthesis, structure, and reactivity of fluorous phosphorus/carbon/phosphorus pincer complexes derived from P(CH2)5P backbones
inferred← citeshttps://doi.org/10.1016/j.ica.2007.05.056openalex-snapshot
Reactivity of fluorinated thioether ligands of the type [C6H4Br-2-(CH2SRF)] towards transition metal complexes of the group 10
inferred← citeshttps://doi.org/10.1016/j.ica.2009.03.003openalex-snapshot
Taylor-made palladium–pincer complexes: A new source of more efficient catalysts for sustainable organic synthesis
inferred← citeshttps://doi.org/10.1016/j.ica.2011.09.034openalex-snapshot
Aliphatic pincer-type POCOP ligands and their complexation behaviour with iridium: Crystal structure of an iridium(III) phosphinite complex
inferred← citeshttps://doi.org/10.1016/j.ica.2011.10.040openalex-snapshot
Palladium and copper complexes with oxygen–nitrogen mixed donors as efficient catalysts for the Heck reaction
inferred← citeshttps://doi.org/10.1016/j.ica.2021.120704openalex-snapshot
Synthesis, photophysical properties and catalytic activity of Ƙ3-SCS pincer palladium (II) complex of N,N'-di-tert-butylbenzene-1,3-dicarbothioamide supported by DFT analysis
inferred← citeshttps://doi.org/10.1016/j.inoche.2008.09.021openalex-snapshot
An unprecedented bonding mode for potassium within a PCP-pincer palladium hydride–K-Selectride® complex
inferred← citeshttps://doi.org/10.1016/j.inoche.2011.05.018openalex-snapshot
Synthesis, structure, and catalytic behavior of a PSiP pincer-type iridium(III) complex
inferred← citeshttps://doi.org/10.1016/j.inoche.2011.10.022openalex-snapshot
Synthesis, characterization, and catalytic behavior of a PSiP pincer-type ruthenium(II) complex
inferred← citeshttps://doi.org/10.1016/j.jcat.2004.05.015openalex-snapshot
Silica and polymer-tethered Pd?SCS-pincer complexes: evidence for precatalyst decomposition to form soluble catalytic species in Mizoroki?Heck chemistry
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2012.12.009openalex-snapshot
An efficient synthesis of perfluoroalkenylated aryl compounds via Pincer-Pd catalyzed Heck couplings
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2003.07.028openalex-snapshot
Phospha-palladacycles and N-heterocyclic carbene palladium complexes: efficient catalysts for CC-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2004.06.007openalex-snapshot
Reaction of aryl di-, tri-, or tetrabromides with arylboronic acids or alkenes in the presence of a palladium-tetraphosphine catalyst
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2004.07.054openalex-snapshot
Palladacycles in catalysis – a critical survey
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2005.02.035openalex-snapshot
1′-Carbopalladated-4-ferrocenyl-1,3-oxazolines as catalysts for Heck reactions: Further evidence in support of the Pd(0)/Pd(II) mechanism
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2005.05.014openalex-snapshot
Selective synthesis of (E)-triethyl(2-arylethenyl)silane derivatives by reaction of aryl bromides with triethyl vinylsilane catalysed by a palladium–tetraphosphine complex
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2005.06.014openalex-snapshot
Kinetic investigation of a PC(sp3)P pincer palladium (II) complex in the Heck reaction
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2006.03.007openalex-snapshot
Predicting the catalytic efficiency by quantum-chemical descriptors: Theoretical study of pincer metallic complexes involved in the catalytic Heck reaction
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2006.07.018openalex-snapshot
Missing link: PCP pincer ligands containing P–N bonds and their Pd complexes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2006.09.055openalex-snapshot
Chiral Pt(II)/Pd(II) pincer complexes that show C–H⋯Cl hydrogen bonding: Synthesis and applications to catalytic asymmetric aldol and silylcyanation reactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2006.12.039openalex-snapshot
Palladacycle as highly efficient catalyst for ring opening of oxabicyclic alkenes with organozinc halides
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.03.020openalex-snapshot
Preparation of NHC-substituted phosphitepalladacycles
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.11.031openalex-snapshot
Isolation and crystallographic characterization of solvate- and anion-stabilized PCP pincer complexes of palladium(II)
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.01.034openalex-snapshot
Density functional study of the complete pathway for the Heck reaction with palladium diphosphines
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.06.016openalex-snapshot
Self-assembly of para-OH functionalized ECE-metalated pincer complexes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.07.003openalex-snapshot
Synthesis and applications of a new palladacycle as a high active catalyst in the Suzuki couplings
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.09.040openalex-snapshot
Palladiumdichloride (ferrocenylethynyl)phosphanes and their use in Pd-catalyzed Heck–Mizoroki- and Suzuki–Miyaura carbon–carbon cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.11.065openalex-snapshot
NC palladacycles in the Heck arylation of ethylene: Synthesis, structure and their reactivity
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.2009.05.025openalex-snapshot
Suzuki reaction catalysed by a PCsp3P pincer Pd(II) complex: Evidence for a mechanism involving molecular species
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2010.10.019openalex-snapshot
New POCOP-type pincer complexes of Nickel(II)
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2010.10.031openalex-snapshot
Structure and catalytic activity of organopalladium(II) complexes based on 4,5-dihydro-1H-imidazol-5-one derivatives
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2011.03.023openalex-snapshot
Application of dimeric cyclopalladated complex of tribenzylamine as an efficient catalyst in the Heck cross-coupling reaction
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2011.03.047openalex-snapshot
Selenoether ligand assisted Heck catalysis
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2011.06.027openalex-snapshot
Cyclometalated complexes derived from calix[4]arene bisphosphites and their catalytic applications in cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2012.07.029openalex-snapshot
Pseudohalide complexes of palladium(II) containing PCP pincer: Synthesis, characterization, and their antimicrobial activities
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2013.01.008openalex-snapshot
Dimethylaminoalkylchalcogenolate complexes of palladium(II): Synthesis, structures, and their catalytic activity in Suzuki C–C cross-coupling reactions
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.2018.09.019openalex-snapshot
(η6-Benzene)Ru(II) half-sandwich complexes of pyrazolated chalcogenoethers for catalytic activation of aldehydes to amides transformation
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2019.04.021openalex-snapshot
Cross-coupling reactions catalysed by palladium pincer complexes. A review of recent advances
inferred← citeshttps://doi.org/10.1016/j.molcata.2003.12.035openalex-snapshot
Comparison of palladium carbene and palladium phosphine catalysts for catalytic coupling reactions of aryl halides
inferred← citeshttps://doi.org/10.1016/j.molcata.2004.04.035openalex-snapshot
Pd-catalyzed Heck arylation of cycloalkenes—studies on selectivity comparing homogeneous and heterogeneous catalysts
inferred← citeshttps://doi.org/10.1016/j.molcata.2004.05.008openalex-snapshot
Bis(triphenylphosphine)palladium(II)phthalimide – an easily prepared precatalyst for efficient Suzuki–Miyaura coupling of aryl bromides
inferred← citeshttps://doi.org/10.1016/j.molcata.2004.07.017openalex-snapshot
Diphosphinoazine palladium(II) complexes as catalysts for the Heck reaction of bromides and an activated chloride
inferred← citeshttps://doi.org/10.1016/j.molcata.2005.01.008openalex-snapshot
Pyridine-derived ruthenium and platinum complexes immobilized on ordered mesoporous silica as catalysts for Heck vinylation
inferred← citeshttps://doi.org/10.1016/j.molcata.2006.05.063openalex-snapshot
Novel silica immobilized NCN-pincer palladium(II) and platinum(II) complexes: Application as Lewis acid catalysts
inferred← citeshttps://doi.org/10.1016/j.molcata.2010.03.014openalex-snapshot
Mechanism of the oxidative addition of hypervalent iodonium salts to palladium(II) pincer-complexes☆
inferred← citeshttps://doi.org/10.1016/j.molcata.2016.09.022openalex-snapshot
Kinetic investigation of cross-coupling reaction steps by advanced competing reaction methods
inferred← citeshttps://doi.org/10.1016/j.molstruc.2017.07.066openalex-snapshot
Supramolecular structures of V(III) complexes supported by PNP pincer ligands
inferred← citeshttps://doi.org/10.1016/j.poly.2006.11.023openalex-snapshot
A highly active two six-membered phosphinite palladium PCP pincer complex [PdCl{C6H3(CH2OPPri)2-2,6}]
inferred← citeshttps://doi.org/10.1016/j.poly.2007.05.031openalex-snapshot
2-Arylnaphthoxazole-derived palladium(II) complexes as phosphine-free catalysts for Heck reactions
inferred← citeshttps://doi.org/10.1016/j.poly.2012.10.006openalex-snapshot
Isolation and X-ray structures of four Rh(PCP) complexes including a Rh(I) dioxygen complex with a short O–O bond
inferred← citeshttps://doi.org/10.1016/j.poly.2015.05.015openalex-snapshot
Cu(II), Zn(II) and Mn(II) complexes of NNS tridentate and Pd(II) complex of NN(μ-S) tetradentate thiobenzyl esters: Synthesis, spectral and X-ray characterization
inferred← citeshttps://doi.org/10.1016/j.poly.2016.09.002openalex-snapshot
Synthesis and structural characterization of Pd(II) and Cu(I) complexes containing dithiophosphorus ligand and their catalytic activities for Heck reaction
inferred← citeshttps://doi.org/10.1016/j.poly.2017.07.020openalex-snapshot
Synthesis and characterization of a NCsp3N pincer complex upon coordination of a bis(pyridine)-functionalized indene
inferred← citeshttps://doi.org/10.1016/j.poly.2020.114415openalex-snapshot
One-pot synthesis of a PCsp3P-type pincer complex via double C H palladation of a large chelate ring
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