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Evidence of the formation of zerovalent palladium from Pd(OAc)2 and triphenylphosphine
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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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Ein neues Katalysatorsystem für die Heck-Reaktion von reaktionsträgen Arylhalogeniden
inferred← citeshttps://doi.org/10.1002/047084289x.rb233openalex-snapshot
Bis(triphenylphosphine)palladium(II) Acetate
inferred← citeshttps://doi.org/10.1002/047084289x.rb233.pub2openalex-snapshot
Bis(triphenylphosphine)palladium(II) Acetate
inferred← citeshttps://doi.org/10.1002/047084289x.ri034openalex-snapshot
Iodo(phenyl)bis(triphenylphosphine)palladium(II)
inferred← citeshttps://doi.org/10.1002/0470857234.ch19openalex-snapshot
Electrophilic Additions to Double Bonds
inferred← citeshttps://doi.org/10.1002/0471264180.or060.02openalex-snapshot
The IntramolecularHeck Reaction
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Homo- and Heterobimetallic Precursor Catalysts for the Heck Reaction, and a Proposal for a General Catalytic Cooperativity Index
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Electrophilic Additions to Double Bonds
inferred← citeshttps://doi.org/10.1002/9780470716076.ch1openalex-snapshot
Mechanisms of the Mizoroki–Heck Reaction
inferred← citeshttps://doi.org/10.1002/9781118754887.ch19openalex-snapshot
Transition Metal‐Catalyzed Carbon–Carbon Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/9783527612222.ch2openalex-snapshot
Cross‐Coupling Reactions of Organoboron Compounds with Organic Halides
inferred← citeshttps://doi.org/10.1002/9783527612222.ch3openalex-snapshot
Palladium‐Catalyzed Coupling of Organyl Halides to Alkenes — the Heck Reaction
inferred← citeshttps://doi.org/10.1002/9783527612222.ch8openalex-snapshot
Palladium‐Catalyzed 1,4‐Additions to Conjugated Dienes
inferred← citeshttps://doi.org/10.1002/9783527618231.ch3bopenalex-snapshot
Development of Methods: Section 3.1.3–3.1.13.4
inferred← citeshttps://doi.org/10.1002/9783527619399.ch2oopenalex-snapshot
Palladium‐Catalyzed Allylic Substitutions
inferred← citeshttps://doi.org/10.1002/9783527619405.ch2nopenalex-snapshot
Palladium‐Catalyzed Allylic Substitutions
inferred← citeshttps://doi.org/10.1002/9783527619535.ch1openalex-snapshot
Mechanistic Aspects of Metal‐Catalyzed C,C‐ and C,X‐Bond‐Forming Reactions
inferred← citeshttps://doi.org/10.1002/9783527619535.ch5openalex-snapshot
Cross‐Coupling of Organyl Halides with Alkenes: the Heck Reaction
inferred← citeshttps://doi.org/10.1002/9783527619535.ch8openalex-snapshot
Palladium‐Catalyzed 1,4‐Additions to Conjugated Dienes
inferred← citeshttps://doi.org/10.1002/9783527623211.ch8openalex-snapshot
Application of Cyclopalladated Compounds as Catalysts for Heck and Sonogashira Reactions
inferred← citeshttps://doi.org/10.1002/9783527655588.ch1openalex-snapshot
Mechanistic Aspects of Metal‐Catalyzed C,C‐ and C,X‐Bond Forming Reactions
inferred← citeshttps://doi.org/10.1002/9783527655588.ch11openalex-snapshot
Palladium‐Catalyzed 1,4‐Additions to Conjugated Dienes
inferred← citeshttps://doi.org/10.1002/9783527655588.ch8openalex-snapshot
Cross‐Coupling of Organyl Halides with Alkenes – The Heck Reaction
inferred← citeshttps://doi.org/10.1002/adsc.200404218openalex-snapshot
A Novel Water‐Soluble m‐TPPTC Ligand: Steric and Electronic Features –Recent Developments in Pd‐ and Rh‐Catalyzed CC Bond Formations
inferred← citeshttps://doi.org/10.1002/adsc.200404298openalex-snapshot
Immobilized Co/Rh Heterobimetallic Nanoparticle‐Catalyzed Pauson–Khand‐Type Reaction
inferred← citeshttps://doi.org/10.1002/adsc.200606045openalex-snapshot
Efficient and Selective Rhodium‐Catalyzed Hydrophosphorylation of Dienes
inferred← citeshttps://doi.org/10.1002/adsc.200900368openalex-snapshot
Intramolecular Palladium‐Catalyzed Direct Arylation vs. Heck Reactions: Synthesis of Pyrroloisoquinolines and Isoindoles
inferred← citeshttps://doi.org/10.1002/adsc.200900590openalex-snapshot
Preparation of Arylphosphonates by Palladium(0)‐Catalyzed Cross‐Coupling in the Presence of Acetate Additives: Synthetic and Mechanistic Studies
inferred← citeshttps://doi.org/10.1002/adsc.201300444openalex-snapshot
Palladium‐Catalyzed Suzuki–Miyaura Cross‐Coupling of α‐Halomethyl Oxime Ethers and Site‐Selective Cross‐Coupling of Dihalo Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.201400075openalex-snapshot
Intramolecular Direct Arylation and Heck Reactions in the Formation of Medium‐Sized Rings: Selective Synthesis of Fused Indolizine, Pyrroloazepine and Pyrroloazocine Systems
inferred← citeshttps://doi.org/10.1002/adsc.201400662openalex-snapshot
Assisted Tandem Palladium(II)/Palladium(0)‐Catalyzed C‐ and N‐Arylations of Quinoxalin‐2(1 H )‐ones in Water
inferred← citeshttps://doi.org/10.1002/adsc.201500332openalex-snapshot
Intermolecular versus Intramolecular Palladium‐Catalyzed Direct Arylations between 1‐(2‐Bromobenzyl)imidazoles and Aryl Bromides
inferred← citeshttps://doi.org/10.1002/adsc.201500778openalex-snapshot
Palladium‐Catalyzed Aminocarbonylation Reaction to Access 1,3,4‐Oxadiazoles using Chloroform as the Carbon Monoxide Source
inferred← citeshttps://doi.org/10.1002/adsc.201500888openalex-snapshot
Mechanistic Studies on the Palladium‐Catalyzed Direct C‐5 Arylation of Imidazoles: The Fundamental Role of the Azole as a Ligand for Palladium
inferred← citeshttps://doi.org/10.1002/adsc.201600708openalex-snapshot
One‐Pot Palladium‐Catalyzed Cross‐Coupling Treble of Borylation, the Suzuki Reaction and Amination
inferred← citeshttps://doi.org/10.1002/adsc.201800258openalex-snapshot
Palladium‐Catalyzed Domino Dehydrogenation/Heck‐Type Reactions of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/adsc.201901100openalex-snapshot
Palladium‐Catalyzed Domino Heck/Phosphorylation towards 3,3‐Disubstituted Phosphinonyloxindoles
inferred← citeshttps://doi.org/10.1002/adsc.202200384openalex-snapshot
Allylic C(sp3)−C(sp3) Bond Formation Through Pd‐Catalyzed C(sp3)−H Activation of Alkenes and 1,4‐Dienes
inferred← citeshttps://doi.org/10.1002/adsc.202300903openalex-snapshot
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
inferred← citeshttps://doi.org/10.1002/adsc.202300921openalex-snapshot
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
inferred← citeshttps://doi.org/10.1002/adsc.202301001openalex-snapshot
Palladium Catalysis: Dependence of the Efficiency of C−C Bond Formation on Carboxylate Ligand and Alkali Metal Carboxylate or Carboxylic Acid Additive. Part C: The Domino Diarylation and Annelation Reactions
inferred← citeshttps://doi.org/10.1002/adsu.202100409openalex-snapshot
Predesigned Covalent Organic Frameworks as Effective Platforms for Pd(II) Coordination Enabling Cross‐Coupling Reactions under Sustainable Conditions
inferred← citeshttps://doi.org/10.1002/aic.15063openalex-snapshot
Engineering uniform nanocrystals: Mechanism of formation and self‐assembly into bimetallic nanocrystal superlattices
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Palladiumkatalysierte Reaktionen von Propargylverbindungen in der organischen Synthese
inferred← citeshttps://doi.org/10.1002/ange.19971091331openalex-snapshot
Synthese und katalytische Wirkung von dendritischen Diphosphan‐Metallkomplexen
inferred← citeshttps://doi.org/10.1002/ange.200300638openalex-snapshot
Die Mechanismen der Stille‐Reaktion
inferred← citeshttps://doi.org/10.1002/ange.200461920openalex-snapshot
Evidence for the Structure of the Enantioactive Ligand in the Phosphine–Copper‐Catalyzed Addition of Diorganozinc Reagents to Imines
inferred← citeshttps://doi.org/10.1002/ange.200501582openalex-snapshot
Tetraarylphosphonium Halides as Arylating Reagents in Pd‐Catalyzed Heck and Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/ange.201210252openalex-snapshot
The Impact of Palladium(II) Reduction Pathways on the Structure and Activity of Palladium(0) Catalysts
inferred← citeshttps://doi.org/10.1002/ange.201303850openalex-snapshot
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
inferred← citeshttps://doi.org/10.1002/ange.201304893openalex-snapshot
Palladium‐Catalyzed Hydrobenzylation of ortho‐Tolyl Alkynyl Ethers by Benzylic CH Activation: Remarkable Alkynoxy‐Directing Effect
inferred← citeshttps://doi.org/10.1002/ange.201311198openalex-snapshot
Aryl Formate as Bifunctional Reagent: Applications in Palladium‐Catalyzed Carbonylative Coupling Reactions Using In Situ Generated CO
inferred← citeshttps://doi.org/10.1002/ange.201410764openalex-snapshot
Regioselektive Pd‐katalysierte Methoxycarbonylierung von Alkenen unter Verwendung von Paraformaldehyd/Methanol als CO‐Surrogat
inferred← citeshttps://doi.org/10.1002/ange.201908451openalex-snapshot
Synthesis of Carboxylic Acids by Palladium‐Catalyzed Hydroxycarbonylation
inferred← citeshttps://doi.org/10.1002/ange.201915386openalex-snapshot
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.202403484openalex-snapshot
Arylative Ring Expansion of 3‐Vinylazetidin‐3‐Ols and 3‐Vinyloxetan‐3‐Ols to Dihydrofurans by Dual Palladium and Acid Catalysis
inferred← citeshttps://doi.org/10.1002/anie.199525891openalex-snapshot
Palladium‐Catalyzed Reactions of Propargylic Compounds in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/anie.199715261openalex-snapshot
Systhesis and Catalytic Activity of Dendritic Diphosphane Metal Complexes
inferred← citeshttps://doi.org/10.1002/anie.200300638openalex-snapshot
The Mechanisms of the Stille Reaction
inferred← citeshttps://doi.org/10.1002/anie.200461920openalex-snapshot
Evidence for the Structure of the Enantioactive Ligand in the Phosphine–Copper‐Catalyzed Addition of Diorganozinc Reagents to Imines
inferred← citeshttps://doi.org/10.1002/anie.200501582openalex-snapshot
Tetraarylphosphonium Halides as Arylating Reagents in Pd‐Catalyzed Heck and Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/anie.201210252openalex-snapshot
The Impact of Palladium(II) Reduction Pathways on the Structure and Activity of Palladium(0) Catalysts
inferred← citeshttps://doi.org/10.1002/anie.201303850openalex-snapshot
Domino Catalysis: Palladium‐Catalyzed Carbonylation of Allylic Alcohols to β,γ‐Unsaturated Esters
inferred← citeshttps://doi.org/10.1002/anie.201304252openalex-snapshot
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.201311198openalex-snapshot
Aryl Formate as Bifunctional Reagent: Applications in Palladium‐Catalyzed Carbonylative Coupling Reactions Using In Situ Generated CO
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.202403484openalex-snapshot
Arylative Ring Expansion of 3‐Vinylazetidin‐3‐Ols and 3‐Vinyloxetan‐3‐Ols to Dihydrofurans by Dual Palladium and Acid Catalysis
inferred← citeshttps://doi.org/10.1002/aoc.1597openalex-snapshot
Long‐chain silanes as reducing agents part 1: a facile, efficient and selective route to amine and phosphine‐stabilized active Pd‐nanoparticles
inferred← citeshttps://doi.org/10.1002/aoc.1843openalex-snapshot
Miscellaneous applications of ferrocene‐based peptides/amides
inferred← citeshttps://doi.org/10.1002/aoc.2975openalex-snapshot
Room‐temperature carbon–sulfur bond formation from Ni(II) σ‐aryl complex via cleavage of the S–S bond of disulfide moieties
inferred← citeshttps://doi.org/10.1002/aoc.3591openalex-snapshot
Synthesis and catalytic application of Pd complex catalysts: Atom‐efficient cross‐coupling of triarylbismuthines with haloarenes and acid chlorides under mild conditions
inferred← citeshttps://doi.org/10.1002/aoc.6690openalex-snapshot
A rare example of the in situ formation of palladium nanoparticles: The emergence of catalytically active palladium nanoparticles from Pd (II) phosphine complexes in the Suzuki–Miyaura coupling reaction
inferred← citeshttps://doi.org/10.1002/aoc.70515openalex-snapshot
Palladium‐Catalyzed β − Carbonyl Alkylation of α ‐Imino Esters With Allylic/Propargyl Alcohols
inferred← citeshttps://doi.org/10.1002/bkcs.10823openalex-snapshot
A Density Functional Theory Study on the Ligand Substitution Mechanism of a Square Planar Pd Complex
inferred← citeshttps://doi.org/10.1002/cctc.201000137openalex-snapshot
Acceleration of the Rate of the Heck Reaction through UV‐ and Visible‐Light‐Induced Palladium(II) Reduction
inferred← citeshttps://doi.org/10.1002/cctc.201200300openalex-snapshot
Hemilabile BINAP(O) as a Chiral Ligand in Desymmetrizing Mizoroki–Heck Cyclizations
inferred← citeshttps://doi.org/10.1002/cctc.201600433openalex-snapshot
Palladium‐Catalyzed Carbonylation of Indoles using Aryl Formates as Bifunctional Reagents: A Route to Indol‐3‐yl Aryl Ketones
inferred← citeshttps://doi.org/10.1002/cctc.201900830openalex-snapshot
Cooperative Use of Brønsted Acids and Metal Catalysts in Tandem Isomerization Reactions of Olefins
inferred← citeshttps://doi.org/10.1002/cctc.202300288openalex-snapshot
Effect of Flexible Chain Length of Graphene‐Supported Palladium Complex Catalyst on Suzuki‐Miyaura Coupling Activity
inferred← citeshttps://doi.org/10.1002/cctc.202401702openalex-snapshot
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
inferred← citeshttps://doi.org/10.1002/cctc.202501702openalex-snapshot
Operando Spectroscopy and Kinetic Modelling Reveal Dynamic Catalyst Species During Auto‐Oxidation of a Palladium Phosphine System
inferred← citeshttps://doi.org/10.1002/chem.19970030823openalex-snapshot
Palladacycles: Efficient New Catalysts for the Heck Vinylation of Aryl Halides
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
inferred← citeshttps://doi.org/10.1002/chem.201000833openalex-snapshot
Asymmetric CC Bond‐Formation Reaction with Pd: How to Favor Heterogeneous or Homogeneous Catalysis?
inferred← citeshttps://doi.org/10.1002/chem.201001911openalex-snapshot
Kinetic Data for the Transmetalation/Reductive Elimination in Palladium‐Catalyzed Suzuki–Miyaura Reactions: Unexpected Triple Role of Hydroxide Ions Used as Base
inferred← citeshttps://doi.org/10.1002/chem.201001960openalex-snapshot
Bimetallic Catalysis Involving Dipalladium(I) and Diruthenium(I) Complexes
inferred← citeshttps://doi.org/10.1002/chem.201002267openalex-snapshot
Dual Effect of Halides in the Stille Reaction: In Situ Halide Metathesis and Catalyst Stabilization
inferred← citeshttps://doi.org/10.1002/chem.201100210openalex-snapshot
Mechanistic Studies of Pd‐Catalyzed Regioselective Aryl CH Bond Functionalization with Strained Alkenes: Origin of Regioselectivity
inferred← citeshttps://doi.org/10.1002/chem.201101695openalex-snapshot
BINAP versus BINAP(O) in Asymmetric Intermolecular Mizoroki–Heck Reactions: Substantial Effects on Selectivities
inferred← citeshttps://doi.org/10.1002/chem.201200516openalex-snapshot
Mechanistic Origin of Antagonist Effects of Usual Anionic Bases (OH−, CO32−) as Modulated by their Countercations (Na+, Cs+, K+) in Palladium‐Catalyzed Suzuki–Miyaura Reactions
inferred← citeshttps://doi.org/10.1002/chem.201301937openalex-snapshot
Oxidative Addition to Palladium(0) Diphosphine Complexes: Observations of Mechanistic Complexity with Iodobenzene as Reactant
inferred← citeshttps://doi.org/10.1002/chem.201406408openalex-snapshot
Catalyst Activation, Deactivation, and Degradation in Palladium‐Mediated Negishi Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/chem.201602735openalex-snapshot
Exploring the Oxidative‐Addition Pathways of Phenyl Chloride in the Presence of PdII Abnormal N‐Heterocyclic Carbene Complexes: A DFT Study
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.201603431openalex-snapshot
Stability and Unimolecular Reactivity of Palladate(II) Complexes [LnPdR3]− (L=Phosphine, R=Organyl, n=0 and 1)
inferred← citeshttps://doi.org/10.1002/chem.201702703openalex-snapshot
A Combined Experimental/Computational Study of the Mechanism of a Palladium‐Catalyzed Bora‐Negishi Reaction
inferred← citeshttps://doi.org/10.1002/chem.201900451openalex-snapshot
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
inferred← citeshttps://doi.org/10.1002/chem.202402664openalex-snapshot
Cyclization by Intramolecular Suzuki‐Miyaura Cross‐Coupling–A Review
inferred← citeshttps://doi.org/10.1002/chin.200345079openalex-snapshot
Oxidative Addition of Aryl Tosylates to Palladium(0) and Coupling of Unactivated Aryl Tosylates at Room Temperature.
inferred← citeshttps://doi.org/10.1002/cssc.202000407openalex-snapshot
Palladium‐Based Bimetallic Nanocrystal Catalysts for the Direct Synthesis of Hydrogen Peroxide
inferred← citeshttps://doi.org/10.1002/cssc.202002433openalex-snapshot
Formate‐Bicarbonate Cycle as a Vehicle for Hydrogen and Energy Storage
inferred← citeshttps://doi.org/10.1002/ejic.200300069openalex-snapshot
The Use of Conductivity Measurements for the Characterization of Cationic Palladium( II ) Complexes and for the Determination of Kinetic and Thermodynamic Data in Palladium‐Catalyzed Reactions
inferred← citeshttps://doi.org/10.1002/ejic.201402952openalex-snapshot
Halogenolysis of a Nickelalactone Complex Produces β‐Halo‐Anhydrides
inferred← citeshttps://doi.org/10.1002/ejic.201900060openalex-snapshot
Hydrazine‐Free Facile Synthesis of Palladium‐Tetrakis(Triphenylphosphine)
inferred← citeshttps://doi.org/10.1002/ejic.202000750openalex-snapshot
Reactions of Schiff Base‐Substituted Diselenides and ‐tellurides with Ni(II), Pd(II) and Pt(II) Phosphine Complexes
inferred← citeshttps://doi.org/10.1002/ejoc.200200499openalex-snapshot
Carbon−Carbon Bond Formation with Electrogenerated Nickel and Palladium Complexes
inferred← citeshttps://doi.org/10.1002/ejoc.200390029openalex-snapshot
15‐Membered Triolefinic Macrocycles − Catalytic Role of (E,E,E)‐1,6,11‐Tris(arenesulfonyl)‐1,6,11‐triazacyclopentadeca‐3,8,13‐triene Complexes of Palladium(0) in the Presence of Phosphanes
inferred← citeshttps://doi.org/10.1002/ejoc.200600540openalex-snapshot
α‐Amino‐α‐vinyl‐γ‐butyrolactone Derivatives from α‐{[(Trimethylsilyl)methyl]alkylidene}‐γ‐butyrolactones
inferred← citeshttps://doi.org/10.1002/ejoc.200601050openalex-snapshot
Procedures for and Possible Mechanisms of Pd‐Catalyzed Allylations of Primary and Secondary Amines with Allylic Alcohols
inferred← citeshttps://doi.org/10.1002/ejoc.201100143openalex-snapshot
Pd‐Mediated Reactions of Epoxides
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.201500979openalex-snapshot
Synthesis of a 4‐Vinyltetrahydrocarbazole by Palladium‐Catalyzed Asymmetric Allylic Alkylation of Indole‐Containing Allylic Carbonates
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/ejoc.202201018openalex-snapshot
Reppe‐Carbonylation of Alkenes with Carboxylic Acids: A Catalytic and Mechanistic Study
inferred← citeshttps://doi.org/10.1002/ejoc.202201374openalex-snapshot
Highly Chemoselective One‐Step Synthesis of Novel N‐Substituted‐Pyrrolo[3,4‐b]quinoline‐1,3‐diones via Palladium‐Catalyzed Aminocarbonylation/Carbonylative Cyclisation Sequence
inferred← citeshttps://doi.org/10.1002/elan.201000767openalex-snapshot
Highly Efficient and Stable Palladium Nanoparticles Supported on an Ionic Liquid Silica SolGel Modified Electrode
inferred← citeshttps://doi.org/10.1002/hlca.202100162openalex-snapshot
Palladium‐Catalyzed Aminocarbonylation of Aryl Halides with N,N‐Dialkylformamide Acetals
inferred← citeshttps://doi.org/10.1002/jhet.2523openalex-snapshot
Synthesis of Pyridazine Dicarboxamides via Highly Selective Palladium‐catalyzed Aminocarbonylation
inferred← citeshttps://doi.org/10.1002/jhet.2635openalex-snapshot
4‐Amino‐TEMPO as N‐Nucleophile in Palladium‐Catalyzed Aminocarbonylation
inferred← citeshttps://doi.org/10.1002/jhet.5570420728openalex-snapshot
Preparation and reactivity of 5-substituted azepino[3,4-b]indoles
inferred← citeshttps://doi.org/10.1002/jlcr.3932openalex-snapshot
A comparative study on Suzuki‐type 11 C‐methylation of aromatic organoboranes performed in two reaction media
inferred← citeshttps://doi.org/10.1002/pol.20210524openalex-snapshot
Improving the efficiency and sustainability of catalysts for direct arylation polymerization (DArP)
inferred← citeshttps://doi.org/10.1002/slct.201900848openalex-snapshot
Synthesis of 5‐Carboxamidotriazoles via Azide‐Alkyne Cycloaddition–Aminocarbonylation Sequence
inferred← citeshttps://doi.org/10.1002/slct.201903801openalex-snapshot
Facile, High‐Yielding Synthesis of 4‐Functionalised 1,2,3‐Triazoles via Amino‐ and Aryloxycarbonylation
inferred← citeshttps://doi.org/10.1002/slct.202001728openalex-snapshot
Synthesis of 2‐Methylresorcinol‐Based Deepened Cavitands with Chiral Inlet Bearing Steroidal Moieties on the Upper Rim
inferred← citeshttps://doi.org/10.1002/slct.202002093openalex-snapshot
Synthesis of Axially Chiral Carboxamides via Aminocarbonylation of Aryl and Vinyl Iodides with 2,2’‐Diamino‐1,1’‐binaphthalene in the Presence of Palladium Catalysts
inferred← citeshttps://doi.org/10.1002/slct.202002203openalex-snapshot
The Ultrasmall Palladium Nanoparticles Catalyzed Telomerization of CO 2 with 1,3‐Butadiene at Room Temperature: Selective Synthesis of δ ‐Lactone
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/10.1007/978-3-642-01053-8_169openalex-snapshot
Mori–Ban indole synthesis
inferred← citeshttps://doi.org/10.1007/978-3-642-28288-1_2openalex-snapshot
Pd-Catalyzed Telomerization of 1,3-Dienes with Multifunctional Renewable Substrates: Versatile Routes for the Valorization of Biomass-Derived Platform Molecules
inferred← citeshttps://doi.org/10.1007/978-3-662-05336-2_202openalex-snapshot
Mori-Ban indole synthesis
inferred← citeshttps://doi.org/10.1007/978-3-662-65244-2_6openalex-snapshot
Übergangsmetallkatalysierte Kupplungsreaktionen
inferred← citeshttps://doi.org/10.1007/978-3-662-70963-4_6openalex-snapshot
Transition Metal-Catalyzed Coupling Reactions
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/10.1007/978-94-010-0373-5_17openalex-snapshot
ROMP in the Synthesis of Well-Defined Catalytic Supports
inferred← citeshttps://doi.org/10.1007/978-94-011-0355-8_12openalex-snapshot
Rhodium and Palladium Water-Soluble Complexes in the Carbonylation Reactions. Improvement in the Transfer between the Organic and Aqueous Phases
inferred← citeshttps://doi.org/10.1007/s00706-014-1254-1openalex-snapshot
Alkoxycarbonylpiperidines as N-nucleophiles in the palladium-catalyzed aminocarbonylation
inferred← citeshttps://doi.org/10.1007/s00706-015-1535-3openalex-snapshot
Synthesis of 2-(1,4-dioxaspiro[4.5]decan-6-yl)acrylamides from 2-acetylcyclohexanone via palladium-catalysed aminocarbonylation
inferred← citeshttps://doi.org/10.1007/s11144-007-5059-7openalex-snapshot
Palladium-catalysed aminocarbonylation of 17-iodo-5α-androst-16-ene with L-amino acid esters in ionic liquids
inferred← citeshttps://doi.org/10.1007/s11172-021-3064-zopenalex-snapshot
Solvent effect in palladium-catalyzed allylation of norbornadiene
inferred← citeshttps://doi.org/10.1007/s11696-020-01478-7openalex-snapshot
Synthesis of novel pregnane-based 20-carboxamides via palladium-catalysed aminocarbonylation
inferred← citeshttps://doi.org/10.1007/s12034-015-0923-yopenalex-snapshot
Palladium nanoparticle anchored polyphosphazene nanotubes: preparation and catalytic activity on aryl coupling reactions
inferred← citeshttps://doi.org/10.1007/s13233-019-7133-1openalex-snapshot
Triphenylphosphine-Containing Thermo-Responsive Copolymers: Synthesis, Characterization and Catalysis Application
inferred← citeshttps://doi.org/10.1016/0022-328x(94)88182-0openalex-snapshot
Carbonylation of bromobenzene in a biphasic medium catalysed by water-soluble palladium complexes derived from tris(3-sulphophenyl)phosphine
inferred← citeshttps://doi.org/10.1016/0022-328x(95)05539-2openalex-snapshot
Combined oxidative and reductive carbonylation of terminal alkynes with palladium iodide-thiourea catalysts
inferred← citeshttps://doi.org/10.1016/0022-328x(96)06136-0openalex-snapshot
Water soluble phosphines VII. Palladium-catalyzed PC cross coupling reactions between primary or secondary phosphines and functional aryliodides — a novel synthetic route to water soluble phosphines
inferred← citeshttps://doi.org/10.1016/0039-128x(95)00121-6openalex-snapshot
Steroidal alkenylphosphonates via palladium-catalyzed coupling reactions
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/10.1016/0040-4039(95)00770-dopenalex-snapshot
Preparation of N-Formyl- and N-carbomethoxy-2,3-dihydropyrroles by palladium-catalyzed isomerization of the corresponding N-acyl-2,5-dihydropyrrole
inferred← citeshttps://doi.org/10.1016/0040-4039(95)00795-eopenalex-snapshot
Palladium-catalyzed reaction of a malonate anion with a glycine cation equivalent: Bis-phosphine ligands and in situ catalyst formation
inferred← citeshttps://doi.org/10.1016/0040-4039(96)00237-7openalex-snapshot
Remote substituent control of the regioselectivity of the aryl- and vinylpalladation of 7-oxabicyclo[2.2.1]heptenes
inferred← citeshttps://doi.org/10.1016/0040-4039(96)01587-0openalex-snapshot
Enantioselective elimination reaction of a 6,6-membered bicyclic allylic carbonate. Importance of chirality reversal depending on the palladium-chiral phosphine ratio
inferred← citeshttps://doi.org/10.1016/0926-860x(95)00190-5openalex-snapshot
Arylation of acrylonitrile with iodobenzene over Pd/MgO catalyst
inferred← citeshttps://doi.org/10.1016/1381-1169(95)00140-9openalex-snapshot
Coordination chemistry and mechanisms of metal-catalyzed CC-coupling reactions11For Part 6 of this series, see ref. [22] (a).. Part 7. Heck vinylation of aryl halides with n-butyl acrylate: relevance of PC bond cleavage to catalyst deactivation
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00129-1openalex-snapshot
C–C Bond Formation (Part 1) by Addition Reactions: through Carbometallation Catalyzed by Group 8–11 Metals
inferred← citeshttps://doi.org/10.1016/bs.adioch.2018.12.002openalex-snapshot
Schrock vs Fischer carbenes: A quantum chemical perspective
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.apcata.2010.04.039openalex-snapshot
Telomerisation of 1,3-butadiene with glycerol under aqueous biphasic conditions: Influence of the reaction conditions on the products distribution
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.bmc.2008.09.009openalex-snapshot
4-Anilino-7-alkenylquinoline-3-carbonitriles as potent MEK1 kinase inhibitors
inferred← citeshttps://doi.org/10.1016/j.catcom.2015.06.005openalex-snapshot
Synthesis of atropisomeric chiral MeOBIPHEP analogues via Pd-catalyzed P–C coupling — applications to asymmetric Rh-catalyzed C–C bond formations in water
inferred← citeshttps://doi.org/10.1016/j.ccr.2009.08.005openalex-snapshot
Catalytic Pauson–Khand-type reactions and related carbonylative cycloaddition reactions
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.ces.2022.118151openalex-snapshot
Simultaneous hypercrosslinking and functionalization of polyHIPEs for use as coarse powder catalyst supports
inferred← citeshttps://doi.org/10.1016/j.ica.2006.07.019openalex-snapshot
Chiral tetradentate amine and tridentate aminocarbene ligands: Synthesis, reactivity and X-ray structural characterizations
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.jcat.2011.04.009openalex-snapshot
Size- and shape-controlled palladium nanoparticles in a fluorometric Tsuji–Trost reaction
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.2006.02.015openalex-snapshot
Computational study of the transmetalation process in the Suzuki–Miyaura cross-coupling of aryls
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.10.051openalex-snapshot
Synthesis of benzylpalladium complexes through C–O bond cleavage of benzylic carboxylates: Development of a novel palladium-catalyzed benzylation of olefins
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.2014.12.017openalex-snapshot
Ligand effect on direct arylation by CMD process
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2019.03.002openalex-snapshot
Different properties of P,C-donor Pd(II) and Pt(II); spectroscopic and X-ray analysis, catalytic potential and anti-proliferative potency
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.mcat.2017.10.031openalex-snapshot
Influence of base additives on the selectivity of palladium-catalysed aminocarbonylation: Highly selective functionalization of a cavitand scaffold
inferred← citeshttps://doi.org/10.1016/j.mcat.2018.03.015openalex-snapshot
Palladium-catalysed aminocarbonylation/cyclization of iodoalkenes toward N-propargylcarboxamides and oxazoles
inferred← citeshttps://doi.org/10.1016/j.mcat.2020.111239openalex-snapshot
Porous organic polymer-supported palladium catalyst for hydroesterification of olefins
inferred← citeshttps://doi.org/10.1016/j.mcat.2021.111895openalex-snapshot
Theoretical study on the mechanism of C N and C C coupling to form indole catalyzed by Pd(OAc)2
inferred← citeshttps://doi.org/10.1016/j.mencom.2023.02.007openalex-snapshot
Crystal structure of tetrakis(triphenylphosphine)palladium(0)
inferred← citeshttps://doi.org/10.1016/j.micromeso.2015.05.002openalex-snapshot
Good Suzuki-coupling reaction performance of Pd immobilized at the metal-free porphyrin-based covalent organic framework
inferred← citeshttps://doi.org/10.1016/j.micromeso.2021.111336openalex-snapshot
Spontaneous formation and catalysis of highly dispersed Pd0 on *BEA zeolite
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