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Palladacycles in catalysis – a critical survey
135/135 checkable references clean · checked 2026-07-23
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
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The 135 checked references that resolve
resolves10.1002/anie.199518441
Palladacycles as Structurally Defined Catalysts for the Heck Olefination of Chloro‐ and Bromoarenes
resolves10.1055/s-2003-38382
Palladium-Catalyzed IntramolecularArylation Reaction: Mechanism and Application for theSynthesis of Polyarenes
resolves10.1246/bcsj.71.2239
Regioselective Arylation Reactions of Biphenyl-2-ols, Naphthols, and Benzylic Compounds with Aryl Halides under Palladium Catalysis
resolves10.1246/cl.1996.823
Palladium-Catalyzed Coupling Reaction of Salicylaldehydes with Aryl Iodides <i>via</i> Cleavage of the Aldehyde C–H Bond
resolves10.1002/anie.199717401
Palladium‐Catalyzed Regioselective Mono‐ and Diarylation Reactions of 2‐Phenylphenols and Naphthols with Aryl Halides
resolves10.1055/s-2003-39911
Novel Synthesis of Naphthobenzazepinesfrom<i>N</i>-Bromobenzylnaphthylaminesby Regioselective C-H Activation Utilizing the Intramolecular Coordinationof an Amine to Pd
resolves10.1016/S0040-4039(01)02077-9
Palladium-catalyzed α-arylation of aldehydes with aryl bromides
resolves10.1016/S0022-328X(02)01466-3
Intramolecular C_N bond formation in the reductive elimination of ortho-palladated arylhydrazones of acetophenone
resolves10.1039/b307535d
Extended X-ray absorption fine structure (EXAFS) characterisation of dilute palladium homogeneous catalystsElectronic supplementary information (ESI) available: electronic supplementary data (ESI) available: data includes reaction profile for and structural/statistical data from EXAFS analysis of Pd(OAc)2/PBut3 catalysed Heck reaction. See http://www.rsc.org/suppdata/cc/b3/b307535d/
resolves10.1016/j.jorganchem.2003.07.028
Phospha-palladacycles and N-heterocyclic carbene palladium complexes: efficient catalysts for CC-coupling reactions
resolves10.1002/1099-0682(200108)2001:8<1917::AID-EJIC1917>3.0.CO;2-M
Palladacycles − An Old Organometallic Family Revisited: New, Simple, and Efficient Catalyst Precursors for Homogeneous Catalysis
resolves10.1016/S0022-328X(00)00876-7
NC-palladacycles as highly effective cheap precursors for the phosphine-free Heck reactions
resolves10.1002/(SICI)1521-3773(20000103)39:1<165::AID-ANIE165>3.0.CO;2-B
Phosphane-Free Palladium-Catalyzed Coupling Reactions: The Decisive Role of Pd Nanoparticles
resolves10.1002/1099-0682(200105)2001:5<1131::AID-EJIC1131>3.0.CO;2-3
Metallic Palladium in the Heck Reaction: Active Catalyst or Convenient Precursor?
resolves10.1016/S0040-4039(98)01967-4
A highly active phosphine-free catalyst system for Heck reactions of aryl bromides
resolves10.1021/ol035184b
Homeopathic Ligand-Free Palladium as a Catalyst in the Heck Reaction. A Comparison with a Palladacycle
resolves10.1002/1615-4169(200210)344:9<996::AID-ADSC996>3.0.CO;2-J
A Practical Recycle of a Ligand-Free Palladium Catalyst for Heck Reactions
resolves10.1016/S0040-4039(01)01590-8
On the use of phosphine-free PdCl2(SEt2)2 complex as catalyst precursor for the Heck reaction
resolves10.1021/jo034646w
Ligand-Free Heck Reaction: Pd(OAc)<sub>2</sub> as an Active Catalyst Revisited
resolves10.1016/j.tet.2003.12.012
Mizoroki–Heck reaction, catalysis by nitrogen ligand Pd complexes and activation of aryl bromides
resolves10.1039/C39840001287
Palladium-catalysed vinylation of organic halides under solid–liquid phase transfer conditions
resolves10.1016/S0040-4039(98)01135-6
[Pd/Base/QX] catalyst systems for directing Heck-type reactions
resolves10.1016/0040-4020(96)00547-9
On the efficiency of tetraalkylammonium salts in Heck type reactions
resolves10.1002/anie.200353473
In Situ Generation of Highly Active Dissolved Palladium Species from Solid Catalysts—A Concept for the Activation of Aryl Chlorides in the Heck Reaction
resolves10.1016/S0022-328X(98)00941-3
Heck reaction catalyzed by phospha-palladacycles in non-aqueous ionic liquids
resolves10.1002/1521-3765(20011001)7:19<4191::AID-CHEM4191>3.0.CO;2-1
Mechanism of the Heck Reaction Using a Phosphapalladacycle as the Catalyst: Classical versus Palladium(IV) Intermediates
resolves10.1016/0040-4039(96)01442-6
First efficient palladium-catalyzed Heck reactions of aryl bromides with alkyl methacrylate
resolves10.1002/(SICI)1099-0682(199801)1998:1<29::AID-EJIC29>3.0.CO;2-X
Phosphapalladacycle-Catalyzed Heck Reactions for Efficient Synthesis of Trisubstituted Olefins: Evidence for Palladium(0) Intermediates
resolves10.1016/S0022-328X(03)00663-6
Palladium-catalyzed coupling reactions of bromo-substituted phenylphosphine oxides: a facile route to functionalized arylphosphine ligands
resolves10.1002/1099-0690(200007)2000:13<2433::AID-EJOC2433>3.0.CO;2-G
Efficient Synthesis of Six-Membered Ring D Analogues of the Pentacyclic Alkaloid Cephalotaxine by Two Palladium-Catalyzed Reactions
resolves10.1002/1098-1128(200007)20:4<304::AID-MED3>3.0.CO;2-8
Multicomponent domino reactions for the synthesis of biologically active natural products and drugs
resolves10.1055/s-2003-40832
Novel Medium Ring Sized EstradiolDerivatives by Intramolecular Heck Reactions
resolves10.1002/chem.19970030823
Palladacycles: Efficient New Catalysts for the Heck Vinylation of Aryl Halides
resolves10.1016/j.tetlet.2003.08.069
Polystyrene-supported recyclable palladacycle catalyst for Heck, Suzuki and Sonogashira reactions
resolves10.1039/b100328n
Highly efficient C–C coupling reactions using metallated benzylphosphine complexes of palladium
resolves10.1039/b203910a
Synthesis of vinylated 5,10,15,20-tetraphenylporphyrins via Heck-type coupling reaction and their photophysical properties
resolves10.1039/a802642d
Highly active, stable, catalysts for the Heck reaction; further suggestions on the mechanism
resolves10.1002/1521-3773(20000602)39:11<1946::AID-ANIE1946>3.0.CO;2-I
Highly Efficient Phosphapalladacyclic Catalysts for the Hydroarylation of Norbornene
resolves10.1039/b005521m
New highly active chiral phosphapalladacycle catalysts. First isolation and characterization of a Pd(iv) intermediate
resolves10.1016/0022-328X(92)80031-R
Palladacycle formation by electrophilic aromatic substitution, as monitored by 1H NMR spectroscopy
resolves10.1016/0022-328X(95)05738-B
Chemistry of alkylaromatic metallacycles. Regiochemistry of CC coupling in ring opening or enlargement reactions of a palladacycle with alkynes
resolves10.1002/anie.199701191
A Complex Catalytic Cycle Leading to a Regioselective Synthesis of <i>o,o</i>′‐Disubstituted Vinylarenes
resolves10.1016/S0022-328X(99)00093-5
Palladium-catalyzed sequential reactions: a new termination step leading to spirocyclohexadienone formation from p-iodophenol and bicyclo[2.2.1]heptene
resolves10.1016/S0022-328X(99)00582-3
Aromatic arylation via palladacycles: interception of reaction intermediates
resolves10.1016/j.jorganchem.2003.07.011
A new catalytic method for the synthesis of selectively substituted biphenyls containing an oxoalkyl chain
resolves10.1039/a909099a
Symmetrical and unsymmetrical 2,6-dialkyl-1,1′-biaryls by combined catalysis of aromatic alkylation via palladacycles and Suzuki-type coupling
resolves10.1016/S0040-4039(98)02384-3
Palladium-catalyzed coupling of functionalized bromoarenes to a polystyrene-bound aryl tributylstannane
resolves10.1021/ol990872+
Palladium-Catalyzed (Ullmann-Type) Homocoupling of Aryl Halides: A Convenient and General Synthesis of Symmetrical Biaryls via Inter- and Intramolecular Coupling Reactions
resolves10.1016/S0040-4039(98)02175-3
Orthopalladated triarylphosphite complexes as highly efficient catalysts in the Heck reaction
resolves10.1039/a806041j
Orthopalladated triaryl phosphite complexes as highly active catalysts in biaryl coupling reactions
resolves10.1002/chem.200304997
Orthopalladated and ‐platinated Bulky Triarylphosphite Complexes: Synthesis, Reactivity and Application as High‐Activity Catalysts for Suzuki and Stille Coupling Reactions
resolves10.1039/b008470k
Palladacyclic phosphinite complexes as extremely high activity catalysts in the Suzuki reaction
resolves10.1021/ja00264a028
Enhancement of catalytic activity through orthometalation. Synthesis, structure, and catalytic activity of a new orthometalated ruthenium complex
resolves10.1039/b208545n
Thermomorphic fluorous imine and thioether palladacycles as precursors for highly active Heck and Suzuki catalysts; evidence for palladium nanoparticle pathways
resolves10.1021/ja005872f
Observation of Unusual Kinetics in Heck Reactions of Aryl Halides: The Role of Non-Steady-State Catalyst Concentration
resolves10.1021/ja003191e
Kinetic Studies of Heck Coupling Reactions Using Palladacycle Catalysts: Experimental and Kinetic Modeling of the Role of Dimer Species
resolves10.1039/b004502k
Cyclopalladated imine catalysts in Heck arylation: search for the catalytic species
resolves10.1016/S0022-328X(01)00967-6
Cyclopalladated ferrocenylimines: highly active catalysts for Heck reactions
resolves10.1021/ol025790r
Highly Active Thermomorphic Fluorous Palladacycle Catalyst Precursors for the Heck Reaction; Evidence for a Palladium Nanoparticle Pathway
resolves10.1016/S0040-4039(00)01594-X
Aryl–Pd covalently bonded palladacycles, novel amino and oxime catalysts {di-μ-chlorobis(benzaldehydeoxime-6-C,N)dipalladium(II), di-μ-chlorobis(dimethylbenzylamine-6-C,N)dipalladium(II)} for the Heck reaction
resolves10.1021/ol0058644
Oxime Palladacycles: Stable and Efficient Catalysts for Carbon−Carbon Coupling Reactions
resolves10.1002/1615-4169(200202)344:2<172::AID-ADSC172>3.0.CO;2-9
Oxime-Derived Palladium Complexes as Very Efficient Catalysts for the Heck–Mizoroki Reaction
resolves10.1021/jo025619t
Highly Active Oxime-Derived Palladacycle Complexes for Suzuki−Miyaura and Ullmann-Type Coupling Reactions
resolves10.1002/1521-3773(20020104)41:1<179::AID-ANIE179>3.0.CO;2-O
A Convenient Oxime-Carbapalladacycle-Catalyzed Suzuki Cross-Coupling of Aryl Chlorides in Water
resolves10.1016/S0022-328X(02)01727-8
Cross-coupling reactions with boronic acids in water catalysed by oxime-derived palladacycles
resolves10.1039/b211742h
An oxime–carbapalladacycle complex covalently anchored to silica as an active and reusable heterogeneous catalyst for Suzuki cross-coupling in water
resolves10.1021/jo030302u
Oxime Carbapalladacycle Covalently Anchored to High Surface Area Inorganic Supports or Polymers as Heterogeneous Green Catalysts for the Suzuki Reaction in Water
resolves10.1016/S0022-328X(02)01195-6
Cyclopalladated complexes of tertiary arylamines as highly efficient catalysts using in the Heck reactions
resolves10.3987/R-1981-09-1603
Organopalladium (II) Complexes Containing Carbon-bonded Pyridine and Picoline as a Ligand: Preparation, Structures, and Reactions
resolves10.1039/B401077A
A new precatalyst for the Suzuki reaction—a pyridyl-bridged dinuclear palladium complex as a source of mono-ligated palladium(
<scp>0</scp>
)
resolves10.1021/ol027337l
Chloropalladated Propargyl Amine: A Highly Efficient Phosphine-Free Catalyst Precursor for the Heck Reaction
resolves10.1055/s-2003-38755
Phosphine-Free Suzuki-MiyauraReactions Catalyzed by Bishydrazone-Pd-Complex
resolves10.1016/j.tetlet.2004.02.069
Sulfilimine palladacycles: stable and efficient catalysts for carbon–carbon coupling reactions
resolves10.1021/ol0057277
Sulfur-Containing Palladacycles as Catalyst Precursors for the Heck Reaction
resolves10.1021/ol0063048
Sulfur-Containing Palladacycles: Efficient Phosphine-Free Catalyst Precursors for the Suzuki Cross-Coupling Reaction at Room Temperature
resolves10.1016/S0040-4039(00)01472-6
PdCl2(SEt2)2 and Pd(OAc)2: simple and efficient catalyst precursors for the Suzuki cross-coupling reaction
resolves10.1021/om000699h
Synthesis and Catalytic Properties of Configurationally Stable and Non-racemic Sulfur-Containing Palladacycles
resolves10.1002/1521-3773(20011015)40:20<3750::AID-ANIE3750>3.0.CO;2-6
Platinum Group Organometallics Based on “Pincer” Complexes: Sensors, Switches, and Catalysts
resolves10.1021/cr960118r
Cyclometalated Phosphine-Based Pincer Complexes: Mechanistic Insight in Catalysis, Coordination, and Bond Activation
resolves10.1016/S0040-4039(99)01938-3
Heck reactions: a caveat on the use of palladium(II) PCP-type catalysts
resolves10.1016/S0040-4039(99)02181-4
Acetylene-bridged P,C,P′-ligands and corresponding cyclopalladated compounds
resolves10.1016/S1381-1169(03)00158-4
The first synthesis of stable palladium(II) PCP-type catalysts supported on silica—application to the Heck reaction
resolves10.1039/b111487p
Synthesis, characterisation and catalytic investigation of a new type of PC(sp3)P pincer Pd(ii) complex
resolves10.1016/S0040-4039(99)01514-2
The synthesis of a new palladacycle catalyst. Development of a high performance catalyst for Heck reactions
resolves10.1016/S0020-1693(99)00616-7
Highly efficient and regioselective production of trisubstituted alkenes through heck couplings catalyzed by a palladium phosphinito PCP pincer complex
resolves10.1039/b004412l
High yield olefination of a wide scope of aryl chlorides catalyzed by the phosphinito palladium PCP pincer complex: [PdCl{C6H3(OPPri2)2-2,6}]
resolves10.1039/b200453b
Investigations into the Pd-catalysed cross-coupling of phenylacetylene with aryl chlorides: simple one-pot procedure and the effect of ZnCl2 co-catalysisElectronic supplementary information (ESI) available: general experimental, procedure for cross-coupling experiments and characterization data for products. See http://www.rsc.org/suppdata/cc/b2/b200453b/
resolves10.1039/b004793g
Palladium bis(phosphinite) ‘PCP’-pincer complexes and their application as catalysts in the Suzuki reaction
resolves10.1016/S0022-328X(03)00604-1
A structure–activity relationship for pincer palladium(II) complexes — influence of ring-size of metallacycles on the activity in allylic alkylation
resolves10.1002/(SICI)1521-3765(20000117)6:2<353::AID-CHEM353>3.0.CO;2-U
Platinum-Catalysed Allylic Alkylation: Reactivity, Enantioselectivity, and Regioselectivity
resolves10.1021/om030371z
Synthesis of Novel Pd−NCN Pincer Complexes Having Additional Nitrogen Coordination Sites and Their Application as Catalysts for the Heck Reaction
resolves10.1021/om0340600
1,2,4-Triazole-Based Palladium Pincer Complexes. A New Type of Catalyst for the Heck Reaction
resolves10.1021/ja991099g
Tridentate SCS Palladium(II) Complexes: New, Highly Stable, Recyclable Catalysts for the Heck Reaction
resolves10.1039/b312368e
Terminally functionalized polyisobutylene oligomers as soluble supports in catalysisElectronic supplementary information (ESI) available: experimental details for the synthesis and use of the PIB oligomers and catalysts. See http://www.rsc.org/suppdata/cc/b3/b312368e/
resolves10.1002/1521-3773(20021004)41:19<3668::AID-ANIE3668>3.0.CO;2-U
A New Generation of Air Stable, Highly Active Pd Complexes for CC and CN Coupling Reactions with Aryl Chlorides
resolves10.1021/om020941f
The Role of Ligand Transformations on the Performance of Phosphite- and Phosphinite-Based Palladium Catalysts in the Suzuki Reaction
resolves10.1039/b304053d
Phosphine and arsine adducts of N-donor palladacycles as catalysts in the Suzuki coupling of aryl bromides
resolves10.1002/1521-3773(20020415)41:8<1363::AID-ANIE1363>3.0.CO;2-G
A Defined N-Heterocyclic Carbene Complex for the Palladium-Catalyzed Suzuki Cross-Coupling of Aryl Chlorides at Ambient Temperatures
resolves10.1021/ja038631r
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
resolves10.1002/anie.200351325
An N‐Heterocyclic Carbene Ligand with Flexible Steric Bulk Allows Suzuki Cross‐Coupling of Sterically Hindered Aryl Chlorides at Room Temperature
resolves10.1055/s-2003-39881
Saturated N-Heterocyclic CarbeneOxime and Amine Palladacycle Catalysis of the Mizoroki-Heckand the Suzuki Reactions
resolves10.1021/ol034264c
Synthesis, Characterization, and Catalytic Activity of <i>N</i>-Heterocyclic Carbene (NHC) Palladacycle Complexes
resolves10.1021/ol0260831
An Air-Stable Palladium/<i>N</i>-Heterocyclic Carbene Complex and Its Reactivity in Aryl Amination
resolves10.1021/ol026745m
Well-Defined, Air-Stable (NHC)Pd(Allyl)Cl (NHC = N-Heterocyclic Carbene) Catalysts for the Arylation of Ketones
resolves10.1016/j.tetlet.2004.03.138
Suzuki–Miyaura coupling with high turnover number using an N-acyl-N-heterocyclic carbene palladacycle precursor
resolves10.1021/ja983263q
High Enantioselection in the Rearrangement of Allylic Imidates with Ferrocenyl Oxazoline Catalysts
resolves10.1016/S0040-4039(02)02439-5
Preparation of bis[palladacycles] and application to asymmetric aza-Claisen rearrangement of allylic imidates
resolves10.1021/ja037086r
Catalytic Asymmetric Rearrangement of Allylic Trichloroacetimidates. A Practical Method for Preparing Allylic Amines and Congeners of High Enantiomeric Purity
resolves10.1021/ol0271786
Catalytic Asymmetric Rearrangement of Allylic <i>N</i>-Aryl Trifluoroacetimidates. A Useful Method for Transforming Prochiral Allylic Alcohols to Chiral Allylic Amines
resolves10.1002/ejic.200390113
<i>para</i>‐Functionalized NCN‐Pincer Palladium(<scp>II</scp>) Complexes: Synthesis, Catalysis and DFT Calculations
resolves10.1021/ol0494515
Development of Chiral Pincer Palladium Complexes Bearing a Pyrroloimidazolone Unit. Catalytic Use for Asymmetric Michael Addition
resolves10.1002/adsc.200390041
Application of a Homogeneous Dodecakis(NCN‐Pd<sup>II</sup>) Catalyst in a Nanofiltration Membrane Reactor under Continuous Reaction Conditions
resolves10.1021/om0101689
Design and Performance of Rigid Nanosize Multimetallic Cartwheel Pincer Compounds as Lewis-Acid Catalysts
resolves10.1021/ja980901w
Thermodynamics and Mechanism of the Reversible Tin-to-Palladium Transmetalation of the Furyl Group
resolves10.1002/anie.200351477
Palladium‐Catalyzed Electrophilic Substitution via Monoallylpalladium Intermediates
resolves10.1021/ja0391715
Palladium Pincer Complex-Catalyzed Trimethyltin Substitution of Functionalized Propargylic Substrates. An Efficient Route to Propargyl- and Allenyl-Stannanes
The 7 references without a DOI — listed, not checked
no DOI — not checked10.1016/j.jorganchem.2004.07.054_bib20
no DOI — not checked10.1016/j.jorganchem.2004.07.054_bib28
no DOI — not checked10.1016/j.jorganchem.2004.07.054_bib32
no DOI — not checked10.1016/j.jorganchem.2004.07.054_bib33
no DOI — not checked10.1016/j.jorganchem.2004.07.054_bib67
no DOI — not checked10.1016/j.jorganchem.2004.07.054_bib87
no DOI — not checked10.1016/j.jorganchem.2004.07.054_bib128
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