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Rates and Mechanism of the Formation of Zerovalent Palladium Complexes from Mixtures of Pd(OAc)2 and Tertiary Phosphines and Their Reactivity in Oxidative Additions
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On the Influence of the Bite Angle of Bidentate Phosphane Ligands on theRegioselectivity in Allylic Alkylation
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Palladium-Catalyzed Bicyclization of 2-Bromo-1,6-dienes and -1,6-enynes to 5-Membered-Ring-Annelated Vinylcyclopropane Derivatives
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Bis(triphenylphosphine)palladium(II) Acetate
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The IntramolecularHeck Reaction
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Transition Metal‐Catalyzed Carbon–Carbon Cross‐Coupling
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Cross‐Coupling Reactions of Organoboron Compounds with Organic Halides
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Palladium‐Catalyzed Coupling of Organyl Halides to Alkenes — the Heck Reaction
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Intramolecular Heck Reactions in Natural Product Chemistry
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Development of Methods: Section 3.1.3–3.1.13.4
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Mechanistic Aspects of Metal‐Catalyzed C,C‐ and C,X‐Bond‐Forming Reactions
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Metal‐Catalyzed Cross‐Coupling Reactions of Organoboron Compounds with Organic Halides
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Metal‐Catalyzed Cross‐Coupling Reactions
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Case Study of Mechanisms in Synthetic Reactions
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Stille Polycondensation: A Versatile Synthetic Approach to Functional Polymers
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Metal‐Catalyzed Alternating Polymerization Reactions with Carbon Monoxide
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A Novel Water‐Soluble m‐TPPTC Ligand: Steric and Electronic Features –Recent Developments in Pd‐ and Rh‐Catalyzed CC Bond Formations
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Intramolecular Palladium‐Catalyzed Direct Arylation vs. Heck Reactions: Synthesis of Pyrroloisoquinolines and Isoindoles
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Preparation of Arylphosphonates by Palladium(0)‐Catalyzed Cross‐Coupling in the Presence of Acetate Additives: Synthetic and Mechanistic Studies
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Intramolecular Direct Arylation and Heck Reactions in the Formation of Medium‐Sized Rings: Selective Synthesis of Fused Indolizine, Pyrroloazepine and Pyrroloazocine Systems
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Assisted Tandem Palladium(II)/Palladium(0)‐Catalyzed C‐ and N‐Arylations of Quinoxalin‐2(1 H )‐ones in Water
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The Palladium Acetate‐Catalyzed Microwave‐Assisted Hirao Reaction without an Added Phosphorus Ligand as a “Green” Protocol: A Quantum Chemical Study on the Mechanism
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Palladium‐Catalyzed Domino Heck/Phosphorylation towards 3,3‐Disubstituted Phosphinonyloxindoles
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Allylic C(sp3)−C(sp3) Bond Formation Through Pd‐Catalyzed C(sp3)−H Activation of Alkenes and 1,4‐Dienes
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Palladium Catalysis: Dependence of the Efficiency of C−C Bond Formation on Carboxylate Ligand and Alkali Metal Carboxylate or Carboxylic Acid Additive. Part A: the C(sp2)−C(sp2), C(sp2)−C(sp3) and C(sp3)−C(sp3) Bonds
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Palladium Catalysis: Dependence of the Efficiency of C−C Bond Formation on Carboxylate Ligand and Alkali Metal Carboxylate or Carboxylic Acid Additive. Part B: The Hydro(hetero)arylation, Hydroalkenylation and Hydroalkylation Reactions
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Die Mechanismen der Stille‐Reaktion
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Domino Catalysis: Palladium‐Catalyzed Carbonylation of Allylic Alcohols to β,γ‐Unsaturated Esters
inferred← citeshttps://doi.org/10.1002/ange.201304252openalex-snapshot
Phosphane‐Functionalized Cycloheptatrienyl–Cyclopentadienyl Titanium Sandwich Complexes: Phosphorus Ligands with an Integrated Reducing Agent for Palladium(0) Catalyst Generation
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Palladium‐Catalyzed Hydrobenzylation of ortho‐Tolyl Alkynyl Ethers by Benzylic CH Activation: Remarkable Alkynoxy‐Directing Effect
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Formation of Four Different Aromatic Scaffolds from Nitriles through Tandem Divergent Catalysis
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Regioselektive Pd‐katalysierte Methoxycarbonylierung von Alkenen unter Verwendung von Paraformaldehyd/Methanol als CO‐Surrogat
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Synthesis of Carboxylic Acids by Palladium‐Catalyzed Hydroxycarbonylation
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Tailored Palladium Catalysts for Selective Synthesis of Conjugated Enynes by Monocarbonylation of 1,3‐Diynes
inferred← citeshttps://doi.org/10.1002/ange.202008916openalex-snapshot
Direct and Selective Synthesis of Adipic and Other Dicarboxylic Acids by Palladium‐Catalyzed Carbonylation of Allylic Alcohols
inferred← citeshttps://doi.org/10.1002/ange.202108744openalex-snapshot
A Systematic Study of the Effects of Complex Structure on Aryl Iodide Oxidative Addition at Bipyridyl‐Ligated Gold(I) Centers
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Nitrate Reduction for Deaminative Suzuki–Miyaura Coupling of Anilines
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Katalysatoraktivierung als Schlüsselfaktor in Kreuzkupplungen: Raumtemperatur‐Kupplungen schwacher Nukleophile ermöglicht durch [Pd(1‐MeNAP)TFA] 2 Präkatalysatoren
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The Mechanisms of the Stille Reaction
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Evidence for the Structure of the Enantioactive Ligand in the Phosphine–Copper‐Catalyzed Addition of Diorganozinc Reagents to Imines
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Oxindole Synthesis through Intramolecular Nucleophilic Addition of Vinylpalladiums to Aryl Isocyanates
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Synthesis, Structure, and Photophysical Properties of Highly Substituted 8,8a‐Dihydrocyclopenta[a]indenes
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The Impact of Palladium(II) Reduction Pathways on the Structure and Activity of Palladium(0) Catalysts
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Domino Catalysis: Palladium‐Catalyzed Carbonylation of Allylic Alcohols to β,γ‐Unsaturated Esters
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Phosphane‐Functionalized Cycloheptatrienyl–Cyclopentadienyl Titanium Sandwich Complexes: Phosphorus Ligands with an Integrated Reducing Agent for Palladium(0) Catalyst Generation
inferred← citeshttps://doi.org/10.1002/anie.201304893openalex-snapshot
Palladium‐Catalyzed Hydrobenzylation of ortho‐Tolyl Alkynyl Ethers by Benzylic CH Activation: Remarkable Alkynoxy‐Directing Effect
inferred← citeshttps://doi.org/10.1002/anie.201403698openalex-snapshot
Formation of Four Different Aromatic Scaffolds from Nitriles through Tandem Divergent Catalysis
inferred← citeshttps://doi.org/10.1002/anie.201410764openalex-snapshot
Regioselective Pd‐Catalyzed Methoxycarbonylation of Alkenes Using both Paraformaldehyde and Methanol as CO Surrogates
inferred← citeshttps://doi.org/10.1002/anie.201908451openalex-snapshot
Synthesis of Carboxylic Acids by Palladium‐Catalyzed Hydroxycarbonylation
inferred← citeshttps://doi.org/10.1002/anie.201915386openalex-snapshot
Tailored Palladium Catalysts for Selective Synthesis of Conjugated Enynes by Monocarbonylation of 1,3‐Diynes
inferred← citeshttps://doi.org/10.1002/anie.202008916openalex-snapshot
Direct and Selective Synthesis of Adipic and Other Dicarboxylic Acids by Palladium‐Catalyzed Carbonylation of Allylic Alcohols
inferred← citeshttps://doi.org/10.1002/anie.202108744openalex-snapshot
A Systematic Study of the Effects of Complex Structure on Aryl Iodide Oxidative Addition at Bipyridyl‐Ligated Gold(I) Centers
inferred← citeshttps://doi.org/10.1002/anie.202110450openalex-snapshot
Halogen‐Bridged Methylnaphthyl Palladium Dimers as Versatile Catalyst Precursors in Coupling Reactions
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Nitrate Reduction for Deaminative Suzuki–Miyaura Coupling of Anilines
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Unlocking Catalyst Activation as a Critical Bottleneck in Cross‐Coupling Reactions: Room‐Temperature Couplings of Weak Nucleophiles Enabled by [Pd(1‐MeNAP)TFA] 2 Precatalysts
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Long‐chain silanes as reducing agents part 1: a facile, efficient and selective route to amine and phosphine‐stabilized active Pd‐nanoparticles
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Room‐temperature carbon–sulfur bond formation from Ni(II) σ‐aryl complex via cleavage of the S–S bond of disulfide moieties
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A Density Functional Theory Study on the Ligand Substitution Mechanism of a Square Planar Pd Complex
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Acceleration of the Rate of the Heck Reaction through UV‐ and Visible‐Light‐Induced Palladium(II) Reduction
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Cooperative Use of Brønsted Acids and Metal Catalysts in Tandem Isomerization Reactions of Olefins
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Gold Nanoparticle‐Catalyzed Solvent Switchable Selective Partial Reduction of Nitrobenzene to N‐Phenylhydroxylamine and Azoxybenzene
inferred← citeshttps://doi.org/10.1002/cctc.202401825openalex-snapshot
Pd/CeO2 Single‐Atom Catalyst Forms Atypical C4 Product in a Suzuki Reaction with 2,4‐Dibromopyridine
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Isolation of Transmetalation Intermediates in the Stille Cross‐Coupling Reaction of Stannanes: Synthesis of Palladacycles, Ligand Substitution, and Insertion Reactions
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The Effect of Hydrogen Bonding on Allylic Alkylation and Isomerization Reactions in Ionic Liquids
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Active Anionic Zero‐Valent Palladium Catalysts: Characterization by Density Functional Calculations
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Palladium‐Catalyzed Formation of Highly Substituted Naphthalenes from Arene and Alkyne Hydrocarbons
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Deprotonative Metalation of Functionalized Aromatics Using Mixed Lithium–Cadmium, Lithium–Indium, and Lithium–Zinc Species
inferred← citeshttps://doi.org/10.1002/chem.200902654openalex-snapshot
Ring‐Opening Metathesis Polymerization Based Pore‐Size‐Selective Functionalization of Glycidyl Methacrylate Based Monolithic Media: Access to Size‐Stable Nanoparticles for Ligand‐Free Metal Catalysis
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Asymmetric CC Bond‐Formation Reaction with Pd: How to Favor Heterogeneous or Homogeneous Catalysis?
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Bimetallic Catalysis Involving Dipalladium(I) and Diruthenium(I) Complexes
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Mechanistic Studies of Pd‐Catalyzed Regioselective Aryl CH Bond Functionalization with Strained Alkenes: Origin of Regioselectivity
inferred← citeshttps://doi.org/10.1002/chem.201100437openalex-snapshot
Palladium‐Catalyzed Cycloisomerizations of Diarylacetylenes: Synthesis, Structures, and Physical Properties of Highly Substituted Naphthalenes and 8,8 a‐Dihydrocyclopenta[a]indenes
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Deprotonative Metalation of Aromatic Compounds by Using an Amino‐Based Lithium Cuprate
inferred← citeshttps://doi.org/10.1002/chem.201602913openalex-snapshot
Multiple Roles of Isocyanides in Palladium‐Catalyzed Imidoylative Couplings: A Mechanistic Study
inferred← citeshttps://doi.org/10.1002/chem.201702703openalex-snapshot
A Combined Experimental/Computational Study of the Mechanism of a Palladium‐Catalyzed Bora‐Negishi Reaction
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Evidence for a Cooperative Mechanism Involving Two Palladium(0) Centers in the Oxidative Addition of Iodoarenes
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Formation of XPhos‐Ligated Palladium(0) Complexes and Reactivity in Oxidative Additions
inferred← citeshttps://doi.org/10.1002/chem.202203974openalex-snapshot
Base‐Controlled Palladium‐Catalyzed Intramolecular ‘One Substrate ‐ Five Reactions’ of 5‐Benzyl‐1‐(2‐halobenzyl)‐2‐phenyl‐1H‐pyrazol‐3(2H)‐ones
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Quantitative Reactivity Models for Oxidative Addition to L 2 Pd(0): Additional Substrate Classes, Solvents, and Mechanistic Insights
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Planar Chiral P,O‐Compounds Derived from Ferrocenyl Aryl Ethers
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Cycloheptatrienyl Cyclopentadienyl Titanium Phosphane Ligands in Palladium‐Catalyzed Suzuki–Miyaura Cross‐Coupling Reactions
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The Effect of High Pressure on the Heck Reaction − A Contribution to a Deeper Understanding of the Mechanism
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Phosphonylation of 2‐Amino‐ and 2‐Amido‐3‐bromopyridines and 2‐Amino‐3‐chloroquinoxalines with Triethyl Phosphite
inferred← citeshttps://doi.org/10.1002/ejoc.201200918openalex-snapshot
Room‐Temperature Suzuki–Miyaura Coupling of Heteroaryl Chlorides and Tosylates
inferred← citeshttps://doi.org/10.1002/ejoc.201402519openalex-snapshot
Kinetic Data on the Synergetic Role of Amines and Water in the Reduction of Phosphine‐Ligated Palladium(II) to Palladium(0)
inferred← citeshttps://doi.org/10.1002/ejoc.202200663openalex-snapshot
Palladium‐Catalyzed Carbonylation of Allylic Chlorides to β,γ‐Unsaturated Esters/Amides under Mild Conditions
inferred← citeshttps://doi.org/10.1002/ijch.201900067openalex-snapshot
Development of Palladium Precatalysts that Efficiently Generate LPd(0) Active Species
inferred← citeshttps://doi.org/10.1002/jccs.200800017openalex-snapshot
The Nitrogen‐Assisted Triphenylphosphine Displacement of Methylpyridine Ligand in Palladium(II) Complex: Crystal Structures of [Pd(PPh3)2{η1‐C5H3N(CH3)}(Br)] and [Pd(PPh3)Br]2{μ,η2‐C5H3N(CH3)}2
inferred← citeshttps://doi.org/10.1007/128_2009_13openalex-snapshot
Synthesis in the Key of Catellani: Norbornene-Mediated ortho C–H Functionalization
inferred← citeshttps://doi.org/10.1007/3-540-68525-1_8openalex-snapshot
Activation of Otherwise Unreactive C-Cl Bonds
inferred← citeshttps://doi.org/10.1007/3418_019openalex-snapshot
Carbonylation of Ethene in Methanol Catalysed by Cationic Phosphine Complexes of Pd(II): from Polyketones to Monocarbonylated Products
inferred← citeshttps://doi.org/10.1007/978-3-540-46129-6_24openalex-snapshot
Organometallic Complexes in Organic Synthesis Examples of Applications
inferred← citeshttps://doi.org/10.1007/978-3-642-01053-8_169openalex-snapshot
Mori–Ban indole synthesis
inferred← citeshttps://doi.org/10.1007/978-3-662-05336-2_202openalex-snapshot
Mori-Ban indole synthesis
inferred← citeshttps://doi.org/10.1007/978-4-431-65924-2_115openalex-snapshot
Investigation of the Mechanism of Palladium-Catalyzed Reactions by Electrochemistry
inferred← citeshttps://doi.org/10.1007/s10562-010-0342-zopenalex-snapshot
Sulfur-Ligand/Pd-Catalyzed Cross-Coupling Reactions of Aryl Halides with Arylboronic Acids Under Aerobic Conditions
inferred← citeshttps://doi.org/10.1007/s11172-021-3064-zopenalex-snapshot
Solvent effect in palladium-catalyzed allylation of norbornadiene
inferred← citeshttps://doi.org/10.1016/0040-4020(95)00752-topenalex-snapshot
Stereoselective synthesis of perfluoroalkylated (E,E)-dienes from perfluoroalkylated alkynes. the synthesis of fluorinated analogs of lepidoptera pheromones
inferred← citeshttps://doi.org/10.1016/0040-4020(96)00303-1openalex-snapshot
The palladium-catalysed vinylic substitution of vinyl triflates with β-substituted-α,β-unsaturated carbonyl compounds. An application to the synthesis of cardenolides
inferred← citeshttps://doi.org/10.1016/0040-4020(96)00714-4openalex-snapshot
Heck couplings of non-activated alkenes
inferred← citeshttps://doi.org/10.1016/1381-1169(96)00033-7openalex-snapshot
Carbon monoxide-ethylene copolymerization catalyzed by a Pd(AcO)2/dppp/TsOH11dppp = 1,3-bis(diphenylphosphino)propane; TsOH = p-toluenesulfonic acid. system: the promoting effect of water and of the acid
inferred← citeshttps://doi.org/10.1016/b0-08-043748-6/09020-4openalex-snapshot
Metal Complexes as Catalysts for Addition of Carbon Monoxide
inferred← citeshttps://doi.org/10.1016/b978-0-12-813834-2.00005-6openalex-snapshot
Reactivity of P–H Group of H-Phosphinic Acid and Its Derivatives
inferred← citeshttps://doi.org/10.1016/b978-0-12-813834-2.00006-8openalex-snapshot
Reactivity of P–H Group of H-Phosphonic Acid and Its Derivatives
inferred← citeshttps://doi.org/10.1016/b978-0-12-820206-7.00111-6openalex-snapshot
High-Throughput Experimentation in Organometallic Chemistry and Catalysis
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Metallate Complexes of the Late Transition Metals: Organometallic Chemistry 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/bs.apoc.2023.08.001openalex-snapshot
Nickel and palladium catalysed cross-coupling: Factors effecting the oxidative addition step
inferred← citeshttps://doi.org/10.1016/j.apcata.2008.03.007openalex-snapshot
Homogeneous catalytic hydrogenolysis of chlorodifluoromethane
inferred← citeshttps://doi.org/10.1016/j.apcata.2019.05.030openalex-snapshot
Synthesis of methyl β-alkylcarboxylates by Pd/diphosphine-catalyzed methoxycarbonylation of methylenealkanes RCH2CH2C(R)=CH2
inferred← citeshttps://doi.org/10.1016/j.catcom.2013.03.028openalex-snapshot
An efficient protocol for copper- and amine-free Sonogashira reactions catalyzed by mononuclear palladacycle complexes containing bidentate phosphine ligands
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.2006.11.013openalex-snapshot
Monomolecular, nanosized and heterogenized palladium catalysts for the Heck reaction
inferred← citeshttps://doi.org/10.1016/j.ccr.2017.10.012openalex-snapshot
Hydroxide complexes of the late transition metals: Organometallic chemistry and catalysis
inferred← citeshttps://doi.org/10.1016/j.ccr.2021.213860openalex-snapshot
Formation and stabilization of nanosized Pd particles in catalytic systems: Ionic nitrogen compounds as catalytic promoters and stabilizers of nanoparticles
inferred← citeshttps://doi.org/10.1016/j.ica.2013.04.048openalex-snapshot
Palladacycle phosphine complexes as homogeneous catalysts for the Heck cross-coupling reaction at low catalyst loading under aerobic conditions
inferred← citeshttps://doi.org/10.1016/j.inoche.2011.03.042openalex-snapshot
Suzuki cross-coupling of aryl bromides catalyzed by cyrhetrenylphosphine complexes of palladium (II)
inferred← citeshttps://doi.org/10.1016/j.jcat.2022.12.006openalex-snapshot
Pd-catalyzed tandem bis-hydroaminocarbonylation of terminal alkynes for synthesis of N-aryl substituted succinimides with involvement of ionic P, O-hybrid ligand
inferred← citeshttps://doi.org/10.1016/j.jcat.2026.116674openalex-snapshot
Kinetic study and modeling of the process for the methyl pelargonate synthesis by 1-octene methoxycarbonylation using CO and the catalytic system Pd(OAc)2–PPh3–p-toluenesulfonic acid
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2004.02.033openalex-snapshot
Synthesis and structural characterization of mixed carbene-carboxylate complexes of palladium(II)
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2004.05.012openalex-snapshot
Formation of anionic palladium(0) complexes ligated by the trifluoroacetate ion and their reactivity in oxidative addition
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2004.10.053openalex-snapshot
Di- and tri-nuclear molybdenum–palladium complexes bearing strong π-acceptor “P–N–P” ligands, MeN{P(OR)2}2 (R = CH2CF3 or Ph)
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.2011.02.027openalex-snapshot
A DFT study of the mechanism of palladium-catalyzed alkoxycarbonylation and aminocarbonylation of alkynes: Hydride versus amine pathways
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2012.03.014openalex-snapshot
Dual reactivity of O-α-allenyl esters under palladium(0) catalysis: From carbopalladation/allylic alkylation domino sequence to decarboxylative allenylation
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2025.123548openalex-snapshot
Long-chain PdIICoII paddle wheel carboxylate complexes: Synthesis, thermal analysis and electrochemistry
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2026.124271openalex-snapshot
Computational investigation of Pd-catalyzed three-component bisamination reactions with ynamides and diaziridinone: Mechanism and regioselectivity
inferred← citeshttps://doi.org/10.1016/j.micromeso.2021.111336openalex-snapshot
Spontaneous formation and catalysis of highly dispersed Pd0 on *BEA zeolite
inferred← citeshttps://doi.org/10.1016/j.micromeso.2024.113156openalex-snapshot
Pd(OAc)2/P–COF: A phosphine-based COF supported palladium-salt heterogeneous catalyst for Suzuki-Miyaura coupling reactions at ambient conditions
inferred← citeshttps://doi.org/10.1016/j.molcata.2003.10.059openalex-snapshot
Homogeneous catalytic hydrodechlorination of CFC and HCFC compounds
inferred← citeshttps://doi.org/10.1016/j.molcata.2009.05.001openalex-snapshot
On the behavior of amines in the presence of Pd0 and PdII species
inferred← citeshttps://doi.org/10.1016/j.molcata.2011.08.008openalex-snapshot
Water-soluble cis-[(NHC)PdBr2(TPPTS)] catalysts and their applications in Suzuki–Miyaura coupling of aryl chlorides
inferred← citeshttps://doi.org/10.1016/j.tet.2004.12.040openalex-snapshot
Palladium-catalyzed homocoupling of aryl halides in the presence of fluoride
inferred← citeshttps://doi.org/10.1016/j.tet.2005.01.032openalex-snapshot
Copper-free palladium-catalyzed sonogashira-type coupling of aryl halides and 1-aryl-2-(trimethylsilyl)acetylenes
inferred← citeshttps://doi.org/10.1016/j.tet.2005.02.026openalex-snapshot
Palladium-catalysed reactions of alcohols. Part B: Formation of C–C and C–N bonds from unsaturated alcohols
inferred← citeshttps://doi.org/10.1016/j.tet.2005.07.098openalex-snapshot
In situ formation of palladium(0) from a P,C-palladacycle
inferred← citeshttps://doi.org/10.1016/j.tet.2007.11.031openalex-snapshot
Negishi cross-coupling reactions of α-amino acid-derived organozinc reagents and aromatic bromides
inferred← citeshttps://doi.org/10.1016/j.tet.2009.04.096openalex-snapshot
An efficient system for the Pd-catalyzed cross-coupling of amides and aryl chlorides
inferred← citeshttps://doi.org/10.1016/j.tet.2014.04.019openalex-snapshot
The influence of the nature of phosphine ligand on palladium catalysts for cross-coupling of weakly nucleophilic potassium pentafluorophenyltrifluoroborate with ArHal and PhCH2Hal (Hal=Br, Cl)
inferred← citeshttps://doi.org/10.1016/j.tet.2015.09.010openalex-snapshot
Improving reactivity and selectivity of aqueous-based Heck reactions by the local hydrophobicity of phosphine ligands
inferred← citeshttps://doi.org/10.1016/j.tet.2022.133063openalex-snapshot
Cross-dehydrogenative annelation of arynes with C(sp2)–H/N–H or C(sp2)–H/O–H frameworks under Pd or Cu catalysis
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133653openalex-snapshot
One-pot esters synthesis from secondary alcohols and CO catalyzed byPd-phosphine systems
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134256openalex-snapshot
Pd0 catalyst/carboxylic acid-mediated hydrofunctionalization of alkynes and allenes, two plausible hydropalladation mechanisms of a versatile process
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134680openalex-snapshot
Domino syntheses of carbo- and heterocycles from Pd-catalyzed bis-substitutions of allylic bis-carboxylates, -carbonates or –diols
inferred← citeshttps://doi.org/10.1016/j.tet.2026.135407openalex-snapshot
A sustainable approach for P(t-Bu)2Ph-involving Pd-catalyzed Suzuki-Miyaura cross-coupling in water at low catalyst loading
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.05.039openalex-snapshot
Palladium-complex-catalyzed regioselective Markovnikov addition reaction and dehydrogenative double phosphinylation to terminal alkynes with diphenylphosphine oxide
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.06.064openalex-snapshot
Palladium(II) phosphine–ylide complexes as highly efficient pre-catalysts in additive- and amine-free Sonogashira coupling reactions performed under aerobic and low Pd loading conditions
inferred← citeshttps://doi.org/10.1016/s0010-8545(96)01322-7openalex-snapshot
Transition metals in organic synthesis. Highlights for the year 1995
inferred← citeshttps://doi.org/10.1016/s0020-1693(97)06015-5openalex-snapshot
Unexpected bell-shaped effect of the ligand on the rate of the oxidative addition to palladium(0) complexes generated in situ from mixtures of Pd(dba)2 and para-substituted triarylphosphines
inferred← citeshttps://doi.org/10.1016/s0020-1693(98)00366-1openalex-snapshot
NMR investigation of Pd(II)–Pd(0) reduction in the presence of mono- and ditertiary phosphines
inferred← citeshttps://doi.org/10.1016/s0022-0728(96)04901-7openalex-snapshot
Mechanism of the electrochemical oxidation of zero valent palladium complexes
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)00063-2openalex-snapshot
Reactivity of [Pd3(μ-OAc)3(μ,η2-MeSCHCO2Et-C,S)3] in the presence of triphenylphosphine: a model of the early steps of the Pd/PR3-catalysed Heck reaction
inferred← citeshttps://doi.org/10.1016/s0022-328x(01)00916-0openalex-snapshot
Palladium(II) phosphine thiocarboxylates. Structures of cis-Pd(κS-SOCMe)2(dppf) [dppf=1,1′-bis(diphenylphosphino)ferrocene] and trans-Pd(κS-SOCMe)2(PPh3)2
inferred← citeshttps://doi.org/10.1016/s0022-328x(02)01225-1openalex-snapshot
Allyl–palladium complexes with fluorinated benzene thiolate ligands. Examination of the electronic effects in the Pd-catalyzed allylic alkylation reaction with the catalytic system [(η3-C3H5)Pd(μ-SRf)]2/PR3
inferred← citeshttps://doi.org/10.1016/s0022-328x(02)01645-5openalex-snapshot
Isolation and structural characterization of some stable Pd(II) carboxylate complexes supported by 1,1′-bis(diphenylphosphino) ferrocene (dppf)
inferred← citeshttps://doi.org/10.1016/s0022-328x(98)01050-xopenalex-snapshot
Application of palladacycles in Heck type reactions
inferred← citeshttps://doi.org/10.1016/s0022-328x(98)01063-8openalex-snapshot
Mechanistic and kinetic studies of palladium catalytic systems
inferred← citeshttps://doi.org/10.1016/s0040-4020(97)10383-0openalex-snapshot
Allylic protecting groups and their use in a complex environment part II: Allylic protecting groups and their removal through catalytic palladium π-allyl methodology
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)02240-7openalex-snapshot
First examples of a tosylate in the palladium-catalyzed Heck cross coupling reaction
inferred← citeshttps://doi.org/10.1016/s0167-2991(98)80171-7openalex-snapshot
Supported Aqueous Phase Catalysts for the C-C and C-N Bond Formation
inferred← citeshttps://doi.org/10.1016/s0277-5387(99)00398-8openalex-snapshot
The Heck reaction: mechanistic insights and novel ligands
inferred← citeshttps://doi.org/10.1016/s0920-5861(98)00129-1openalex-snapshot
Palladium(0) allylic alkylation in a two-phase system or with a supported aqueous phase catalyst
inferred← citeshttps://doi.org/10.1016/s1045-0688(98)80007-5openalex-snapshot
Synthesis of biaryls via the cross-coupling reaction of arylboronic acids
inferred← citeshttps://doi.org/10.1016/s1381-1169(97)00144-1openalex-snapshot
Complete debromination of polybrominated benzenes at room temperature catalyzed by palladium metallocenyl diphosphine complexes
inferred← citeshttps://doi.org/10.1016/s1381-1169(97)00274-4openalex-snapshot
Room-temperature hydrodebromination of 4,4′-dibromobiphenyl catalyzed by 1,1′-bis(diphenylphosphino)ferrocene complexes of palladium
inferred← citeshttps://doi.org/10.1016/s1381-1169(98)00387-2openalex-snapshot
Palladium(II)-catalyzed synthesis of polyamides (aramids) from aromatic dichlorides, diamines, and carbon monoxide
inferred← citeshttps://doi.org/10.1016/s1381-1169(99)00251-4openalex-snapshot
Hydroesterification of styrene using an in situ formed Pd(OTs)2(PPh3)2 complex catalyst
inferred← citeshttps://doi.org/10.1016/s1460-1567(07)80050-xopenalex-snapshot
Chapter 1 An introduction to palladium catalysis
inferred← citeshttps://doi.org/10.1016/s1872-2067(20)63561-6openalex-snapshot
Intermediate formation enabled regioselective access to amide in the Pd-catalyzed reductive aminocarbonylation of olefin with nitroarene
inferred← citeshttps://doi.org/10.1016/s1873-0418(03)80005-2openalex-snapshot
Activation of Substrates with Polar Single Bonds
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5c00996openalex-snapshot
Metal-Catalyzed Reductive Coupling of Aryl Halides beyond Premetalated Reagents or Metallic Reductants: Biaryl Formation
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.2c04291openalex-snapshot
Mechanistic Insight into Palladium/Brønsted Acid Catalyzed Methoxycarbonylation and Hydromethoxylation of Internal Alkene: A Computational Study
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.9b01392openalex-snapshot
Ligands and Bases Mediate Switching between Aminocarbonylations and Alkoxycarbonylations in Coupling of Aminophenols with Iodoarenes
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00533openalex-snapshot
Mechanism and Origin of Ligand-Controlled Chemo- and Regioselectivities in Palladium-Catalyzed Methoxycarbonylation of Alkynes
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02732openalex-snapshot
Preparation of (E)-1,3-Enyne Derivatives through Palladium Catalyzed Hydroalkynylation of Allenes
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00966openalex-snapshot
Pd(0)/Xantphos-Catalyzed Benzylic C(sp 3 )–O Arylation of Benzyl Heteroaryl Ethers: Reduction of Pd(II) to Pd(0) by Xantphos
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00891openalex-snapshot
Palladium-Catalyzed Denitrogenative Carbonylation of Benzotriazinones in Batch and Flow: Divergent Synthesis of Phthalimides and Phthalic Diamides
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00348openalex-snapshot
Mechanism and Origin of Stereoselectivity of Pd-Catalyzed Cascade Annulation of Aryl Halide, Alkene, and Carbon Monoxide via C–H Activation
inferred← citeshttps://doi.org/10.1021/acs.jpca.0c06746openalex-snapshot
Exploring Phosphine Electronic Effects on Molybdenum Complexes: A Combined Photoelectron Spectroscopy and Energy Decomposition Analysis Study
inferred← citeshttps://doi.org/10.1021/acs.oprd.2c00332openalex-snapshot
Kinetic and Mechanistic Investigations to Enable a Key Suzuki Coupling for Sotorasib Manufacture─What a Difference a Base Makes
inferred← citeshttps://doi.org/10.1021/acs.oprd.3c00200openalex-snapshot
Investigation of Mechanochemical Sonogashira Couplings─From Batch Solution to Continuous Reactive Extrusion through Ball-Milling Optimization
inferred← citeshttps://doi.org/10.1021/acs.oprd.9b00170openalex-snapshot
Development of an Operational Space Using Mechanistic Models for a Pd-Catalyzed Amidation Reaction Used in the Synthesis of ABT-530
inferred← citeshttps://doi.org/10.1021/acs.organomet.0c00117openalex-snapshot
Revisiting the Palladium-Catalyzed Carbonylation of Allyl Alcohol: Mechanistic Insight and Improved Catalytic Efficiency
inferred← citeshttps://doi.org/10.1021/acs.organomet.1c00090openalex-snapshot
Role of dppf Monoxide in the Transmetalation Step of the Suzuki–Miyaura Coupling Reaction
inferred← citeshttps://doi.org/10.1021/acs.organomet.1c00347openalex-snapshot
Reactivity of a Dinuclear Pd I Complex [Pd 2 (μ-PPh 2 )(μ 2 -OAc)(PPh 3 ) 2 ] with PPh 3 : Implications for Cross-Coupling Catalysis Using the Ubiquitous Pd(OAc) 2 /nPPh 3 Catalyst System
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