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Palladium-Catalyzed Reppe Carbonylation

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

inferredcites →https://doi.org/10.1002/0470021209openalex-snapshot
Palladium Reagents and Catalysts
inferredcites →https://doi.org/10.1002/9783527619351openalex-snapshot
Applied Homogeneous Catalysis with Organometallic Compounds
inferredcites →https://doi.org/10.1002/anie.196700921openalex-snapshot
Oxygen Complexes of Zerovalent Nickel, Palladium, and Platinum
inferredcites →https://doi.org/10.1002/anie.196803291openalex-snapshot
Carbonylation of Olefins under Mild Temperature Conditions in the Presence of Palladium Complexes
inferredcites →https://doi.org/10.1002/anie.196803351openalex-snapshot
Sulfonyl Hydrazones of Cyclic Amides and Quaternary Azo Sulfones of Heterocycles as Reagents in Azo Chemistry
inferredcites →https://doi.org/10.1002/anie.199317201openalex-snapshot
Phosphinic Acid‐Based C2‐Symmetrical Inhibitors of HIV‐Protease**
inferredcites →https://doi.org/10.1002/jlac.19535820102openalex-snapshot
Carbonylierung I. Über die Umsetzung von Acetylen mit Kohlenoxyd und Verbindungen mit reaktionsfähigen Wasserstoffatomen Synthesen α,β‐ungesättigter Carbonsäuren und ihrer Derivate
inferredcites →https://doi.org/10.1002/jlac.19535820103openalex-snapshot
Carbonylierung II. Carbonsäuren und ihre Derivate aus olefinischen Verbindungen und Kohlenoxyd
inferredcites →https://doi.org/10.1002/jlac.19535820104openalex-snapshot
Carbonylierung III. Umsetzung von Alkoholen und offenen Äthern mit Kohlenoxyd zu Carbonsäuren
inferredcites →https://doi.org/10.1002/jlac.19535820105openalex-snapshot
Carbonylierung IV. Einwirkung von Kohlenoxyd und Wasser auf cyclische Äther
inferredcites →https://doi.org/10.1002/jlac.19535820106openalex-snapshot
Carbonylierung V. Zur Kenntnis der Metallcarbonyle und Metallcarbonylwasserstoffe
inferredcites →https://doi.org/10.1002/jlac.19535820107openalex-snapshot
Carbonylierung VI. Synthesen mit Metallcarbonylwasserstoffen
inferredcites →https://doi.org/10.1002/recl.19961150411openalex-snapshot
“Green” MMA; an environmentally benign and economically attractive process for the production of methyl methacrylate
inferredcites →https://doi.org/10.1007/978-3-642-67452-5openalex-snapshot
New Syntheses with Carbon Monoxide
inferredcites →https://doi.org/10.1007/978-3-642-67452-5_3openalex-snapshot
Carbonylations Catalyzed by Metal Carbonyls-Reppe Reactions
inferredcites →https://doi.org/10.1007/978-3-642-67475-4openalex-snapshot
Organic Synthesis with Palladium Compounds
inferredcites →https://doi.org/10.1007/bf01024186openalex-snapshot
Advances in catalytic carbonylation with transition metal complexes in homogeneous phase
inferredcites →https://doi.org/10.1007/bf02067988openalex-snapshot
Palladium(II)-catalyzed hydroesterification of enol esters: Remarkable α-substituent effect upon regioselectivity
inferredcites →https://doi.org/10.1007/bf02668492openalex-snapshot
Linear carboxylic acid esters from α‐olefins: 3. Catalysis by dispersions of palladium complexes
inferredcites →https://doi.org/10.1007/bf02886865openalex-snapshot
Catalytic carboxylation of fats. Carboxy acids and esters from monounsaturates
inferredcites →https://doi.org/10.1016/0021-9517(79)90065-4openalex-snapshot
Syngas reactions I. The catalytic carbonylation of conjugated dienes
inferredcites →https://doi.org/10.1016/0022-328x(85)87240-5openalex-snapshot
Metals in organic syntheses
inferredcites →https://doi.org/10.1016/0022-328x(90)87014-5openalex-snapshot
On the mechanism of the hydrocarbalkoxylation of olefins catalyzed by palladium complexes
inferredcites →https://doi.org/10.1016/0022-328x(91)80176-kopenalex-snapshot
Efficient palladium catalysts for the copolymerization of carbon monoxide with olefins to produce perfectly alternating polyketones
inferredcites →https://doi.org/10.1016/0022-328x(93)80406-2openalex-snapshot
Efficient palladium catalysts for the carbonylation of alkynes
inferredcites →https://doi.org/10.1016/0022-328x(94)84007-5openalex-snapshot
Homogeneous catalysis by cationic palladium complexes. Precision catalysis in the carbonylation of alkynes
inferredcites →https://doi.org/10.1016/0022-328x(94)87088-8openalex-snapshot
First use of methyl formate with no extra carbon monoxide in the hydroesterification of ethene catalysed by palladium complexes
inferredcites →https://doi.org/10.1016/0022-328x(94)87106-xopenalex-snapshot
Carbon monoxide as a building block in organic synthesis. Part V. Involvement of palladium-hydride species in carbonylation reactions of monoterpenes. X-ray crystal structure of [Ph3PCH2CHCHPh]4[PdCl6][SnCl6]
inferredcites →https://doi.org/10.1016/0022-328x(94)88055-7openalex-snapshot
New aspects of the carbonylation of allylpalladium complexes
inferredcites →https://doi.org/10.1016/0143-7208(87)85030-1openalex-snapshot
Ullmann's Encyclopedia of Industrial Chemistry
inferredcites →https://doi.org/10.1016/0304-5102(79)80018-8openalex-snapshot
Metals in organic syntheses I. Propene hydrocarboxylation with various alkanols and PdCl2(PPh3)2 as catalyst precursor
inferredcites →https://doi.org/10.1016/0304-5102(81)85004-3openalex-snapshot
Metal in organic synthesis. VI. The solvent effect on the hydrocarbonalkoxylation of propene promoted by a [PdCl2(PPh3)2]−PPh3 catalyst precursor
inferredcites →https://doi.org/10.1016/0304-5102(85)80007-9openalex-snapshot
Metals in organic syntheses
inferredcites →https://doi.org/10.1016/0304-5102(85)85022-7openalex-snapshot
Applications of the water-gas shift reaction. use of the CO/H2O couple for the conversion of variolls organic substrates catalyzed by transition metal complexes
inferredcites →https://doi.org/10.1016/0304-5102(89)80080-xopenalex-snapshot
Determination of key intermediates for homogeneous water-gas shift reaction and hydrocarbonylation of ethylene to diethyl ketone catalyzed by the ‘Pd(OAc)2-PPh3-CF3COOH/H2O’ system
inferredcites →https://doi.org/10.1016/0304-5102(90)85045-jopenalex-snapshot
Levulinic acid synthesis via regiospecific carbonylation of methyl vinyl ketone ob of its reaction products with hydrochloric ach) or an alkanol or of a mixture of acetone with a formaldehyde precursor catalyzed by a highly active Pd-HCl system
inferredcites →https://doi.org/10.1016/0304-5102(92)80191-iopenalex-snapshot
Effect of solvent on the kinetics of hydroformylation of 1-hexene using HRh(CO)(PPh3)3 catalyst
inferredcites →https://doi.org/10.1016/0304-5102(93)87064-fopenalex-snapshot
Carbon monoxide as a building block in organic synthesis
inferredcites →https://doi.org/10.1016/0304-5102(93)e0324-aopenalex-snapshot
Palladium-catalyzed hydroesterification of alkynes in the presence of p-toluenesulfonic acid under a normal pressure of carbon monoxide
inferredcites →https://doi.org/10.1016/1381-1169(95)00115-8openalex-snapshot
Synthesis of γ-ketocycloalkanecarboxylic acid esters by region-specific alkoxy carbonylation of α,β-ketocycloolefins catalyzed by palladium
inferredcites →https://doi.org/10.1016/1381-1169(95)00130-1openalex-snapshot
Progress in hydroformylation and carbonylation
inferredcites →https://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
inferredcites →https://doi.org/10.1016/s0022-328x(00)89120-2openalex-snapshot
Hydrocarbo alkoxylation of N-vinylphthalimide catalyzed by palladium complexes
inferredcites →https://doi.org/10.1016/s0022-328x(00)90871-4openalex-snapshot
Alkoxy carbonyl complexes of palladium and their role in alcohol carbonylation
inferredcites →https://doi.org/10.1016/s0022-328x(00)93181-4openalex-snapshot
Metals in orgranic syntheses
inferredcites →https://doi.org/10.1016/s0022-328x(00)93732-xopenalex-snapshot
Asymmetric hydrocarboxylation of olefins
inferredcites →https://doi.org/10.1016/s0022-328x(97)00092-2openalex-snapshot
Hydroesterification of ethylene catalyzed by Pd(II) complexes: an ab initio MO study
inferredcites →https://doi.org/10.1016/s0022-328x(97)00241-6openalex-snapshot
Asymmetric hydroesterification of styrene by PdCl2-CuCl2-chiral phosphine catalyst systems
inferredcites →https://doi.org/10.1016/s0022-328x(98)01217-0openalex-snapshot
A study on the catalytic pathways of the hydroalkoxycarbonylation reaction of styrene
inferredcites →https://doi.org/10.1016/s0022-328x(99)00225-9openalex-snapshot
Comparative investigation of the regioselectivity in styrene and α-methylstyrene hydroalkoxycarbonylation as a function of palladium catalyst structure
inferredcites →https://doi.org/10.1016/s0040-4039(00)73391-0openalex-snapshot
Synthesis of unsaturated acids by 1,2-addition of formic acid to conjugated dienes catalyzed by palladium on carbon in the presence of mono and bidentate phosphines
inferredcites →https://doi.org/10.1016/s0040-4039(00)94174-1openalex-snapshot
Selective hydroesterification of alkynes to mono- or diesters
inferredcites →https://doi.org/10.1016/s0920-5861(98)00357-5openalex-snapshot
Copolymerization of ethylene and carbon monoxide using [(dppp)Pd(H2O)(TsO)](TsO) as a catalyst precursor: rate equation
inferredcites →https://doi.org/10.1016/s0920-5861(98)00379-4openalex-snapshot
Chemically modified β-cyclodextrins in biphasic catalysis: a fruitful contribution of the host–guest chemistry to the transition-metal catalyzed reactions
inferredcites →https://doi.org/10.1016/s1381-1169(96)00192-6openalex-snapshot
Catalytic conversions in water. Part 411For part 3 of this series see Ref. [18].: Carbonylation of 5-hydroxymethylfurfural (HMF) and benzyl alcohol catalysed by palladium trisulfonated triphenylphosphine complexes
inferredcites →https://doi.org/10.1016/s1381-1169(96)00385-8openalex-snapshot
Hydroesterification of styrene catalyzed by montmorillonite-diphenylphosphinepalladium(II) chloride in the presence of chiral phosphines
inferredcites →https://doi.org/10.1016/s1381-1169(96)00396-2openalex-snapshot
A palladium complex catalyst for the regioselective hydrocarboxylation of 4-methylstyrene
inferredcites →https://doi.org/10.1016/s1381-1169(98)00166-6openalex-snapshot
Hydroformylation of ethene with triphenylphosphine modified rhodium catalyst: kinetic and mechanistic studies
inferredcites →https://doi.org/10.1016/s1387-7003(98)00079-3openalex-snapshot
Highly selective hydrocarboxylation of styrene with oxalic acid or water using palladium ortho-amino arenethiolates with intramolecular coordinating nitrogen Lewis bases
inferredcites →https://doi.org/10.1021/ar00155a007openalex-snapshot
Aspects of intermediacy of carbalkoxymetal complexes in carbon monoxide reactions
inferredcites →https://doi.org/10.1021/ar00170a006openalex-snapshot
New aspects of oxypalladation of alkenes
inferredcites →https://doi.org/10.1021/ar50061a002openalex-snapshot
Addition reactions of butadiene catalyzed by palladium complexes
inferredcites →https://doi.org/10.1021/cr00089a002openalex-snapshot
New aspects of carbonylations catalyzed by transition metal complexes
inferredcites →https://doi.org/10.1021/cr940282jopenalex-snapshot
Palladium-Catalyzed Alternating Copolymerization of Alkenes and Carbon Monoxide
inferredcites →https://doi.org/10.1021/cr950272yopenalex-snapshot
Hydrido Complexes of Palladium
inferredcites →https://doi.org/10.1021/ie970621+openalex-snapshot
Kinetics of Carboxylation of Styrene Using a Homogeneous Palladium Complex Catalyst
inferredcites →https://doi.org/10.1021/ja00075a076openalex-snapshot
Synthesis and identification by high-pressure NMR spectroscopy of the cationic square-planar cis-methyl(carbonyl)palladium diphosphine compound [Pd(CH3)(CO)[(S,S)-BDPP]]BF4, an intermediate in CO insertion into the Pd-Me bond
inferredcites →https://doi.org/10.1021/ja00163a053openalex-snapshot
Asymmetric synthesis of acids by the palladium-catalyzed hydrocarboxylation of olefins in the presence of (R)-(-)- or (S)-(+)-1,1'-binaphthyl-2,2'-diyl hydrogen phosphate
inferredcites →https://doi.org/10.1021/ja00205a039openalex-snapshot
Chelate-assisted, palladium-catalyzed efficient carbonylation of aryl chlorides
inferredcites →https://doi.org/10.1021/ja00205a040openalex-snapshot
Direct observation of .beta.-hydride elimination reactions on metal surfaces
inferredcites →https://doi.org/10.1021/ja01018a074openalex-snapshot
Electrolytic reduction of molecular nitrogen
inferredcites →https://doi.org/10.1021/jo00005a047openalex-snapshot
An investigation of the palladium-catalyzed, formate-mediated hydroxycarbonylation of optically active 1-arylethyl esters
inferredcites →https://doi.org/10.1021/jo00005a048openalex-snapshot
Preparation of 3-amino-4-(hydroxymethyl)azetidin-2-ones from the reaction of glycine enolates with imines of a glycoaldehyde
inferredcites →https://doi.org/10.1021/jo00169a040openalex-snapshot
Regioselective hydroesterification and hydrocarboxylation of 3,3,3-trifluoropropene and pentafluorostyrene catalyzed by phosphine-palladium complex
inferredcites →https://doi.org/10.1021/jo00169a041openalex-snapshot
Regioselectivity of 1,3-dipolar cycloadditions of (phenylsulfinyl)- and (phenylsulfonyl)alkenes
inferredcites →https://doi.org/10.1021/jo00879a020openalex-snapshot
Linear carboxylic acid esters from .alpha. olefins. 2. Catalysis by homogeneous palladium complexes
inferredcites →https://doi.org/10.1021/jo00879a021openalex-snapshot
Stereochemistry of reduction of ketones by simple and complex metal hydrides of the main group elements
inferredcites →https://doi.org/10.1021/jo00958a026openalex-snapshot
Noble metal catalysis. II. Hydratocarbonylation reaction of olefins with carbon monoxide to give saturated acids
inferredcites →https://doi.org/10.1021/ma951313vopenalex-snapshot
Catalytic Hydrocarboxylation and Hydroesterification Reactions of 1,2-Polybutadiene
inferredcites →https://doi.org/10.1021/ma960829ropenalex-snapshot
A Novel Approach to α,β-Unsaturated Acrylated Polymers from Poly(2-methylvinylacetylene) by Homogeneous Catalysis
inferredcites →https://doi.org/10.1021/om00017a084openalex-snapshot
Formation of Dinuclear Palladium(I) Hydride [Pd2(.mu.-H)(.mu.-CO){(S,S)-BDPP}2]Cl by Methanolysis or Hydrolysis of Pd(COMe)(Cl){(S,S)-BDPP} {(S,S)-BDPP = (2S,4S)-2,4-Bis(diphenylphosphino)pentane}
inferredcites →https://doi.org/10.1021/om00027a022openalex-snapshot
Palladium-catalyzed hydrocarboxylation of alkynes with formic acid
inferredcites →https://doi.org/10.1021/om00037a011openalex-snapshot
Selectivity of the carbonylation of styrene by cationic palladium complexes
inferredcites →https://doi.org/10.1021/om00054a070openalex-snapshot
Palladium chloride catalyzed dicarbonylation of terminal alkynes
inferredcites →https://doi.org/10.1021/om00150a041openalex-snapshot
Palladium chloride-catalyzed olefin-formate ester carbonylation reactions. A simple, exceptionally mild, and regioselective route to branched chain carboxylic esters
inferredcites →https://doi.org/10.1021/om9607513openalex-snapshot
Regioselective Cyclocarboxylation of Nonconjugated Dienes to Cyclic Keto Esters
inferredcites →https://doi.org/10.1023/a:1019015912635openalex-snapshot
Catalytic conversions in water. Part 6. A novel biphasic hydrocarboxylation of olefins catalyzed by palladium TPPTS complexes (TPPTS=P(C6H4-m-SO3Na) 3)
inferredcites →https://doi.org/10.1023/a:1019019119363openalex-snapshot
Comment on ``Catalytic conversion in water. Part 6. A novel biphasic hydrocarboxylation of olefins catalyzed by palladium TPPTS complexes (TPPTS=P(C6H4-m-SO3Na)3)''
inferredcites →https://doi.org/10.1023/a:1019073231967openalex-snapshot
Palladium-catalyzed hydroesterification of propene into methyl 2-methylpropanoate at room temperature and atmospheric pressure. Influence of various parameters on the activity and selectivity of the reaction
inferredcites →https://doi.org/10.1038/physci239013b0openalex-snapshot
Studies of Palladium and Platinum Triphenylphosphine Complexes with Carbon Monoxide at High Pressures
inferredcites →https://doi.org/10.1039/9781847556509-00384openalex-snapshot
Homogeneous catalysis
inferredcites →https://doi.org/10.1039/dt9800002246openalex-snapshot
Hard ligands as donors to soft metals. Part 3. Cationic bis(solvent) complexes of palladium(II); cations for catalysis
inferredcites →https://doi.org/10.1039/jm9920201149openalex-snapshot
Analysis of the composition of polycarboxylic acids obtained by catalytic hydrocarboxylation of polybutadienes
inferredcites →https://doi.org/10.1039/jm9930300019openalex-snapshot
Polycarboxylic acids via catalytic hydrocarboxylation of polybutadienes
inferredcites →https://doi.org/10.1055/s-1991-20800openalex-snapshot
Hydroesterification of 6-Methoxy-2-naphthylethene
inferredcites →https://doi.org/10.1111/j.1398-9995.1978.tb01551.xopenalex-snapshot
Announcements
inferredcites →https://doi.org/10.1111/j.1749-6632.1983.tb47355.xopenalex-snapshot
THE REMARKABLY MILD, REGIOSPECIFIC, AND CATALYTIC HOMOGENEOUS HYDROESTERIFICATION OF OLEFINS*
inferredcites →https://doi.org/10.1246/bcsj.49.2245openalex-snapshot
Kinetics on the Carbonylation of Cyclohexene in a Methanol Solution Catalyzed by Palladium(II) Chloride–Triphenylphosphine
inferredcites →https://doi.org/10.1246/bcsj.63.640openalex-snapshot
A Facile, Practical Synthesis of 2-(6-Methoxy-2-naphthyl)propenoic Acid
inferredcites →https://doi.org/10.1246/bcsj.64.3600openalex-snapshot
Selective Mono- and Bis(alkoxycarbonylation)s of Olefins Catalyzed by Palladium in the Presence of Cu(I) or Cu(II) Chloride under Remarkably Mild Conditions. Application to the Synthesis of γ-Butyrolactone Derivatives
inferredcites →https://doi.org/10.1246/cl.1996.339openalex-snapshot
Asymmetric Hydroesterification of Norbornene by Chiral Non-chelate Biphosphine Palladium Complexes

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Effect of Cerium Morphology on the Catalytic Activity of Ru/Ceria on the Methoxycarbonylation of Ethylene
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Carbon Monoxide
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Carbonylation Processes by Homogeneous CatalysisBased in part on the article Carbonylation Processes by Homogeneous Catalysis by George G. Stanley which appeared in the Encyclopedia of Inorganic Chemistry, First Edition .
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Palladium: Organometallic Chemistry
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Fine Chemical Synthesis – Homogeneous
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Carbonylation
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Reppe Carbonylation
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Cobalt‐Catalyzed Carbonylation Reactions
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Preparation of Acid Derivatives and Anhydrides
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Preparation of Acid Derivatives and Anhydrides
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Poly(vinylpyridine)
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Carbonylation and Related Reactions
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Carbonylation and Carboxylation
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Carbonylation Processes by Homogeneous CatalysisBased in part on the article Carbonylation Processes by Homogeneous Catalysis by George G. Stanley which appeared in the Encyclopedia of Inorganic Chemistry, First Edition .
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Palladium: Organometallic Chemistry
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Recent Developments in Alkyne Carbonylation
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Carbonyl Compounds from Alkynes and Alkenes
inferred← citeshttps://doi.org/10.1002/9783527809080.cataz08452openalex-snapshot
hydrocarboxylation
inferred← citeshttps://doi.org/10.1002/9783527809080.cataz14298openalex-snapshot
Reppe syntheses
inferred← citeshttps://doi.org/10.1002/9783527829354.ch1openalex-snapshot
Introduction: Carbon Monoxide as Synthon in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/9783527829354.ch3openalex-snapshot
Nickel‐Catalyzed Carbonylations
inferred← citeshttps://doi.org/10.1002/9783527829354.ch8openalex-snapshot
Palladium( II )‐Catalyzed Carbonylations
inferred← citeshttps://doi.org/10.1002/9783527831883.ch13openalex-snapshot
Asymmetric Carbonylation Reactions
inferred← citeshttps://doi.org/10.1002/9783527831883.ch8openalex-snapshot
Recent Hydrocarbonylation of Unsaturated Hydrocarbons with Homogeneous Catalyst
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0151openalex-snapshot
CH Functionalization Utilizing CO Surrogates
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Palladium‐Catalyzed Hydroesterification of Alkynes Employing Aryl Formates without the Use of External Carbon Monoxide
inferred← citeshttps://doi.org/10.1002/adsc.201000772openalex-snapshot
Rhodium‐Catalysed Alkoxycarbonylative Cyclisation Reactions of 1,6‐Enynes
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Carbonylative Tertiary Amide Synthesis from Aryl Iodides and Tertiary Amines via Oxidant‐Free C−N Bond Cleavage Catalyzed by Palladium(II) Chloride in Polyethylene Glycol/Water
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Mechanistic Insight into Weak Base‐Catalyzed Generation of Carbon Monoxide from Phenyl Formate and Its Application to Catalytic Carbonylation at Room Temperature without Use of External Carbon Monoxide Gas
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Metal‐free Carbon Monoxide (CO) Capture and Utilization: Formylation of Amines
inferred← citeshttps://doi.org/10.1002/adsc.201901383openalex-snapshot
Palladium Catalysed Acid‐Free Carboxytelomerisation of 1,3‐Butadiene with Alcohols Accessing Pelargonic Acid Derivatives Including Triglycerides under Selectivity Control
inferred← citeshttps://doi.org/10.1002/adsc.202000500openalex-snapshot
Recent Advances in Carbonylative Difunctionalization of Alkenes
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Counterion Effects Enable Divergent Pd‐Catalyzed Carbonylative Cyclization of Amide‐Tethered o‐Alkynylphenols
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Ambient Hydrocarbonylation of Olefins Enabled by Visible‐Light
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Ligand‐Assisted Pd‐Catalyzed N‐Dealkylative Carbonylation of Tertiary Amines with (Hetero)Aryl Halides to Tertiary Amides
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Palladium‐Catalyzed Carbonylation of Aryl Sulfonium Salts with CO 2 as a CO Surrogate
inferred← citeshttps://doi.org/10.1002/ajoc.202400261openalex-snapshot
Multi‐Dentate Phosphine Ligand Derived from Cyclotetrasiloxane and Its Application in Palladium‐Catalyzed Alkoxycarbonylation of Alkenes
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Examination of Heterogenized Triphenylphosphine‐Palladium Catalysts for Methoxycarbonylation of Higher Olefins
inferred← citeshttps://doi.org/10.1002/ajoc.202500569openalex-snapshot
LiCl‐Promoted Branched Methoxycarbonylation of Propylene Using a Heterogenized Triphenylphosphine‐palladium Catalyst
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Katalytische Carbonylierungen: kein Bedarf an Kohlenmonoxid
inferred← citeshttps://doi.org/10.1002/ange.200702889openalex-snapshot
Aluminum Triflate as a Highly Active and Efficient Nonprotic Cocatalyst in the Palladium‐Catalyzed Methoxycarbonylation Reaction
inferred← citeshttps://doi.org/10.1002/ange.201005823openalex-snapshot
Eine allgemeine und selektive Eisen‐katalysierte Aminocarbonylierung von Alkinen: Synthese von Acryl‐ und Zimtsäureamiden
inferred← citeshttps://doi.org/10.1002/ange.201208330openalex-snapshot
Alternative Metalle für die homogen katalysierte Hydroformylierung
inferred← citeshttps://doi.org/10.1002/ange.201308455openalex-snapshot
Selective Palladium‐Catalyzed Aminocarbonylation of Olefins with Aromatic Amines and Nitroarenes
inferred← citeshttps://doi.org/10.1002/ange.201400059openalex-snapshot
Reduktive Aminierung ohne externe Wasserstoffquelle
inferred← citeshttps://doi.org/10.1002/ange.201404563openalex-snapshot
Palladium‐Catalyzed Alkoxycarbonylation of Conjugated Dienes under Acid‐Free Conditions: Atom‐Economic Synthesis of β,γ‐Unsaturated Esters
inferred← citeshttps://doi.org/10.1002/ange.201502405openalex-snapshot
Palladium‐Catalyzed Hydroaminocarbonylation of Alkenes with Amines: A Strategy to Overcome the Basicity Barrier Imparted by Aliphatic Amines
inferred← citeshttps://doi.org/10.1002/ange.201503954openalex-snapshot
Palladium‐Catalyzed Hydroamidocarbonylation of Olefins to Imides
inferred← citeshttps://doi.org/10.1002/ange.201601803openalex-snapshot
Die Wassergas‐Shift‐Reaktion in der organischen Synthese
inferred← citeshttps://doi.org/10.1002/ange.201605104openalex-snapshot
Selective Palladium‐Catalyzed Aminocarbonylation of Olefins to Branched Amides
inferred← citeshttps://doi.org/10.1002/ange.201612520openalex-snapshot
Übergangsmetallkatalysierte Nutzung von Methanol als C1‐Quelle in der organischen Synthese
inferred← citeshttps://doi.org/10.1002/ange.201700317openalex-snapshot
Efficient Palladium‐Catalyzed Alkoxycarbonylation of Bulk Industrial Olefins Using Ferrocenyl Phosphine Ligands
inferred← citeshttps://doi.org/10.1002/ange.201701950openalex-snapshot
Palladium‐Catalyzed Carbonylation of sec‐ and tert‐Alcohols
inferred← citeshttps://doi.org/10.1002/ange.201706794openalex-snapshot
Markovnikov‐Selective Palladium Catalyst for Carbonylation of Alkynes with Heteroarenes
inferred← citeshttps://doi.org/10.1002/ange.201709807openalex-snapshot
Liganden‐ und lösungsmittelkontrollierte regio‐ und chemodivergente Carbonylierungen
inferred← citeshttps://doi.org/10.1002/ange.201803797openalex-snapshot
Katalytische, isofunktionelle Reaktionen – Erweiterung des Repertoires an Shuttle‐ und Metathesereaktionen
inferred← citeshttps://doi.org/10.1002/ange.201813801openalex-snapshot
Pd‐Catalyzed Selective Carbonylation of gem‐Difluoroalkenes: A Practical Synthesis of Difluoromethylated Esters
inferred← citeshttps://doi.org/10.1002/ange.201905905openalex-snapshot
Palladium‐Catalyzed Enantioselective Thiocarbonylation of Styrenes
inferred← citeshttps://doi.org/10.1002/ange.202015329openalex-snapshot
Efficient Palladium‐Catalyzed Carbonylation of 1,3‐Dienes: Selective Synthesis of Adipates and Other Aliphatic Diesters
inferred← citeshttps://doi.org/10.1002/ange.202015450openalex-snapshot
Asymmetric Hydroesterification of Diarylmethyl Carbinols
inferred← citeshttps://doi.org/10.1002/ange.202105977openalex-snapshot
Asymmetric Alkoxy‐ and Hydroxy‐Carbonylations of Functionalized Alkenes Assisted by β‐Carbonyl Groups
inferred← citeshttps://doi.org/10.1002/ange.202106079openalex-snapshot
Ligand‐Controlled Regiodivergent Thiocarbonylation of Alkynes toward Linear and Branched α,β‐Unsaturated Thioesters
inferred← citeshttps://doi.org/10.1002/ange.202107856openalex-snapshot
Palladium‐Catalyzed Asymmetric Markovnikov Hydroxycarbonylation and Hydroalkoxycarbonylation of Vinyl Arenes: Synthesis of 2‐Arylpropanoic Acids
inferred← citeshttps://doi.org/10.1002/ange.202200733openalex-snapshot
Nickel‐Catalyzed Asymmetric Hydroaryloxy‐ and Hydroalkoxycarbonylation of Cyclopropenes
inferred← citeshttps://doi.org/10.1002/ange.202207970openalex-snapshot
Nickel‐Catalyzed Four‐Component Carbonylation of Ethers and Olefins: Direct Access toγ‐Oxy Esters and Amides
inferred← citeshttps://doi.org/10.1002/ange.202211939openalex-snapshot
Iron‐Catalyzed Alkoxycarbonylation of Alkyl Bromides via a Two‐Electron Transfer Process
inferred← citeshttps://doi.org/10.1002/ange.202214706openalex-snapshot
Efficient Synthesis of Novel Plasticizers by Direct Palladium‐Catalyzed Di‐ or Multi‐carbonylations
inferred← citeshttps://doi.org/10.1002/ange.202307570openalex-snapshot
Palladium and Ruthenium Dual‐Single‐Atom Sites on Porous Ionic Polymers for Acetylene Dialkoxycarbonylation: Synergetic Effects Stabilize the Active Site and Increase CO Adsorption
inferred← citeshttps://doi.org/10.1002/ange.202410967openalex-snapshot
Palladium‐Catalyzed Enantioselective Migratory Hydroamidocarbonylation of Amide‐Linked Alkenes to Access Chiral α‐Alkyl Succinimides
inferred← citeshttps://doi.org/10.1002/ange.202412828openalex-snapshot
Cobalt‐Catalyzed Intramolecular Markovnikov Hydrocarbonylation of Unactivated Alkenes via Hydrogen Atom Transfer
inferred← citeshttps://doi.org/10.1002/ange.202509228openalex-snapshot
Light‐Driven Ligand Exchange for Palladium‐Catalyzed Regiodivergent Transfer Hydrothiocarbonylation
inferred← citeshttps://doi.org/10.1002/ange.202512346openalex-snapshot
Iron‐Catalyzed Carbonylation Reactions with Carbon Monoxide
inferred← citeshttps://doi.org/10.1002/anie.200301736openalex-snapshot
Evolution of Carbonylation Catalysis: No Need for Carbon Monoxide
inferred← citeshttps://doi.org/10.1002/anie.200702889openalex-snapshot
Aluminum Triflate as a Highly Active and Efficient Nonprotic Cocatalyst in the Palladium‐Catalyzed Methoxycarbonylation Reaction
inferred← citeshttps://doi.org/10.1002/anie.201005823openalex-snapshot
A General and Selective Iron‐Catalyzed Aminocarbonylation of Alkynes: Synthesis of Acryl‐ and Cinnamides
inferred← citeshttps://doi.org/10.1002/anie.201208330openalex-snapshot
Alternative Metals for Homogeneous Catalyzed Hydroformylation Reactions
inferred← citeshttps://doi.org/10.1002/anie.201308455openalex-snapshot
Selective Palladium‐Catalyzed Aminocarbonylation of Olefins with Aromatic Amines and Nitroarenes
inferred← citeshttps://doi.org/10.1002/anie.201400059openalex-snapshot
Reductive Amination without an External Hydrogen Source
inferred← citeshttps://doi.org/10.1002/anie.201404563openalex-snapshot
Palladium‐Catalyzed Alkoxycarbonylation of Conjugated Dienes under Acid‐Free Conditions: Atom‐Economic Synthesis of β,γ‐Unsaturated Esters
inferred← citeshttps://doi.org/10.1002/anie.201502405openalex-snapshot
Palladium‐Catalyzed Hydroaminocarbonylation of Alkenes with Amines: A Strategy to Overcome the Basicity Barrier Imparted by Aliphatic Amines
inferred← citeshttps://doi.org/10.1002/anie.201503954openalex-snapshot
Palladium‐Catalyzed Hydroamidocarbonylation of Olefins to Imides
inferred← citeshttps://doi.org/10.1002/anie.201601803openalex-snapshot
Harnessing the Power of the Water‐Gas Shift Reaction for Organic Synthesis
inferred← citeshttps://doi.org/10.1002/anie.201605104openalex-snapshot
Selective Palladium‐Catalyzed Aminocarbonylation of Olefins to Branched Amides
inferred← citeshttps://doi.org/10.1002/anie.201612520openalex-snapshot
Transition‐Metal‐Catalyzed Utilization of Methanol as a C1 Source in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/anie.201700317openalex-snapshot
Efficient Palladium‐Catalyzed Alkoxycarbonylation of Bulk Industrial Olefins Using Ferrocenyl Phosphine Ligands
inferred← citeshttps://doi.org/10.1002/anie.201701950openalex-snapshot
Palladium‐Catalyzed Carbonylation of sec‐ and tert‐Alcohols
inferred← citeshttps://doi.org/10.1002/anie.201706794openalex-snapshot
Markovnikov‐Selective Palladium Catalyst for Carbonylation of Alkynes with Heteroarenes
inferred← citeshttps://doi.org/10.1002/anie.201709807openalex-snapshot
Ligand‐ and Solvent‐Controlled Regio‐ and Chemodivergent Carbonylative Reactions
inferred← citeshttps://doi.org/10.1002/anie.201803797openalex-snapshot
Catalytic Isofunctional Reactions—Expanding the Repertoire of Shuttle and Metathesis Reactions
inferred← citeshttps://doi.org/10.1002/anie.201813801openalex-snapshot
Pd‐Catalyzed Selective Carbonylation of gem‐Difluoroalkenes: A Practical Synthesis of Difluoromethylated Esters
inferred← citeshttps://doi.org/10.1002/anie.201905905openalex-snapshot
Palladium‐Catalyzed Enantioselective Thiocarbonylation of Styrenes
inferred← citeshttps://doi.org/10.1002/anie.202015329openalex-snapshot
Efficient Palladium‐Catalyzed Carbonylation of 1,3‐Dienes: Selective Synthesis of Adipates and Other Aliphatic Diesters
inferred← citeshttps://doi.org/10.1002/anie.202015450openalex-snapshot
Asymmetric Hydroesterification of Diarylmethyl Carbinols
inferred← citeshttps://doi.org/10.1002/anie.202105977openalex-snapshot
Asymmetric Alkoxy‐ and Hydroxy‐Carbonylations of Functionalized Alkenes Assisted by β‐Carbonyl Groups
inferred← citeshttps://doi.org/10.1002/anie.202106079openalex-snapshot
Ligand‐Controlled Regiodivergent Thiocarbonylation of Alkynes toward Linear and Branched α,β‐Unsaturated Thioesters
inferred← citeshttps://doi.org/10.1002/anie.202107856openalex-snapshot
Palladium‐Catalyzed Asymmetric Markovnikov Hydroxycarbonylation and Hydroalkoxycarbonylation of Vinyl Arenes: Synthesis of 2‐Arylpropanoic Acids
inferred← citeshttps://doi.org/10.1002/anie.202200733openalex-snapshot
Nickel‐Catalyzed Asymmetric Hydroaryloxy‐ and Hydroalkoxycarbonylation of Cyclopropenes
inferred← citeshttps://doi.org/10.1002/anie.202207970openalex-snapshot
Nickel‐Catalyzed Four‐Component Carbonylation of Ethers and Olefins: Direct Access toγ‐Oxy Esters and Amides
inferred← citeshttps://doi.org/10.1002/anie.202211939openalex-snapshot
Iron‐Catalyzed Alkoxycarbonylation of Alkyl Bromides via a Two‐Electron Transfer Process
inferred← citeshttps://doi.org/10.1002/anie.202214706openalex-snapshot
Efficient Synthesis of Novel Plasticizers by Direct Palladium‐Catalyzed Di‐ or Multi‐carbonylations
inferred← citeshttps://doi.org/10.1002/anie.202307570openalex-snapshot
Palladium and Ruthenium Dual‐Single‐Atom Sites on Porous Ionic Polymers for Acetylene Dialkoxycarbonylation: Synergetic Effects Stabilize the Active Site and Increase CO Adsorption
inferred← citeshttps://doi.org/10.1002/anie.202410967openalex-snapshot
Palladium‐Catalyzed Enantioselective Migratory Hydroamidocarbonylation of Amide‐Linked Alkenes to Access Chiral α‐Alkyl Succinimides
inferred← citeshttps://doi.org/10.1002/anie.202412828openalex-snapshot
Cobalt‐Catalyzed Intramolecular Markovnikov Hydrocarbonylation of Unactivated Alkenes via Hydrogen Atom Transfer
inferred← citeshttps://doi.org/10.1002/anie.202509228openalex-snapshot
Light‐Driven Ligand Exchange for Palladium‐Catalyzed Regiodivergent Transfer Hydrothiocarbonylation
inferred← citeshttps://doi.org/10.1002/anie.202512346openalex-snapshot
Iron‐Catalyzed Carbonylation Reactions with Carbon Monoxide
inferred← citeshttps://doi.org/10.1002/aoc.1046openalex-snapshot
Palladium‐catalyzed selective alkoxycarbonylation of N‐vinylphthalimide
inferred← citeshttps://doi.org/10.1002/aoc.1433openalex-snapshot
Palladium–dppb–borate‐catalyzed regioselective synthesis of cinnamate esters by alkoxycarbonylation of phenylacetylene
inferred← citeshttps://doi.org/10.1002/aoc.3137openalex-snapshot
Methoxycarbonylation of olefins catalyzed by palladium(II) complexes containing naphthyl(diphenyl)phosphine ligands
inferred← citeshttps://doi.org/10.1002/aoc.5175openalex-snapshot
Structural and theoretical studies of the methoxycarbonylation of higher olefins catalysed by (Pyrazolyl‐ethyl)pyridine palladium (II) complexes
inferred← citeshttps://doi.org/10.1002/aoc.6391openalex-snapshot
The intriguing methoxycarbonylation of trimethylsilylacetylene in the presence of Drent's catalytic system
inferred← citeshttps://doi.org/10.1002/aoc.6439openalex-snapshot
Sterically hindered (pyridyl)benzamidine palladium(II) complexes: Syntheses, structural studies, and applications as catalysts in the methoxycarbonylation of olefins
inferred← citeshttps://doi.org/10.1002/aoc.7893openalex-snapshot
Arylhydrazone‐Thioeter Palladium Pincer Complexes Catalyzed Carbonylative Suzuki–Miyaura Cross‐Coupling Using Fe(CO)5 as CO Surrogate
inferred← citeshttps://doi.org/10.1002/asia.201301636openalex-snapshot
Synthesis of New Diphosphine Ligands and their Application in Pd‐Catalyzed Alkoxycarbonylation Reactions
inferred← citeshttps://doi.org/10.1002/asia.201403260openalex-snapshot
Synthesis of Acylphosphonates by a Palladium‐Catalyzed Phosphonocarbonylation Reaction of Aryl Iodides with Phosphites
inferred← citeshttps://doi.org/10.1002/asia.202101127openalex-snapshot
Steric Influence on Reactions of Benzyl Potassium Species with CO
inferred← citeshttps://doi.org/10.1002/asia.202400892openalex-snapshot
Silver‐Catalyzed Carbamoylation and Carbonylative Cyclization of Alkenes with Oxamic Acids
inferred← citeshttps://doi.org/10.1002/cctc.200900062openalex-snapshot
Palladium‐Catalyzed Carbonylation Reactions of Alkenes and Alkynes
inferred← citeshttps://doi.org/10.1002/cctc.201100238openalex-snapshot
Pd/Al(OTf)3 Catalyzed Methoxycarbonylation: On the Importance of Counterions and the Acid Source
inferred← citeshttps://doi.org/10.1002/cctc.201402304openalex-snapshot
Ruthenium‐Catalyzed Alkoxycarbonylation of Alkenes with Paraformaldehyde as a Carbon Monoxide Substitute
inferred← citeshttps://doi.org/10.1002/cctc.201402986openalex-snapshot
Imidazole Derivatives as Accelerators for Ruthenium‐Catalyzed Hydroesterification and Hydrocarbamoylation of Alkenes: Extensive Ligand Screening and Mechanistic Study
inferred← citeshttps://doi.org/10.1002/cctc.201500356openalex-snapshot
Functionalized Magnetic Mesoporous Silica Nanoparticle‐Supported Palladium Catalysts for Carbonylative Sonogashira Coupling Reactions of Aryl Iodides
inferred← citeshttps://doi.org/10.1002/cctc.201500464openalex-snapshot
An Empirical Study of Phosphine Ligands for the Methoxycarbonylation of Medium‐Chain Alkenes
inferred← citeshttps://doi.org/10.1002/cctc.201500824openalex-snapshot
Palladium‐Catalyzed Aminocarbonylation of Aliphatic Alkenes with N,N‐Dimethylformamide as an In Situ Source of CO
inferred← citeshttps://doi.org/10.1002/cctc.201501423openalex-snapshot
Branched Selectivity in the Pd‐Catalysed Methoxycarbonylation of 1‐Alkenes
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.202100051openalex-snapshot
One‐Pot Palladium‐Catalyzed Carbonylative Sonogashira Coupling using Carbon Dioxide as Carbonyl Source
inferred← citeshttps://doi.org/10.1002/cctc.202101594openalex-snapshot
The One‐pot Encapsulation of Palladium Complexes into Covalent Organic Frameworks Enables the Alkoxycarbonylation of Olefins
inferred← citeshttps://doi.org/10.1002/cctc.202402000openalex-snapshot
Exploring the Catalytic Efficiency of Phosphine CN ‐Palladacycles in the Alkoxycarbonylation of Styrene: Optimization and Scope
inferred← citeshttps://doi.org/10.1002/chem.200501398openalex-snapshot
The Mechanism of the Hydroalkoxycarbonylation of Ethene and Alkene–CO Copolymerization Catalyzed by PdII–Diphosphine Cations
inferred← citeshttps://doi.org/10.1002/chem.200700839openalex-snapshot
Rhodium‐Catalyzed [2+2+1+1] Cyclocarbonylative Coupling of Alkynes with Carbon Monoxide Affording Tetrasubstituted p‐Benzoquinones
inferred← citeshttps://doi.org/10.1002/chem.200900563openalex-snapshot
The AZARYPHOS Family of Ligands for Ambifunctional Catalysis: Syntheses and Use in Ruthenium‐Catalyzed anti‐Markovnikov Hydration of Terminal Alkynes
inferred← citeshttps://doi.org/10.1002/chem.200903158openalex-snapshot
Phosphine Ligands in the Palladium‐Catalysed Methoxycarbonylation of Ethene: Insights into the Catalytic Cycle through an HP NMR Spectroscopic Study
inferred← citeshttps://doi.org/10.1002/chem.201100447openalex-snapshot
Microwave‐Assisted Aminocarbonylation of Ynamides by Using Catalytic [Fe3(CO)12] at Low Pressures of Carbon Monoxide
inferred← citeshttps://doi.org/10.1002/chem.201404462openalex-snapshot
Palladium‐Catalyzed Carbonylative [3+2+1] Annulation of N‐Aryl‐Pyridine‐2‐Amines with Internal Alkynes by CH Activation: Facile Synthesis of 2‐Quinolinones
inferred← citeshttps://doi.org/10.1002/chem.201503785openalex-snapshot
Direct Synthesis of an α,ω‐Diester from 2,7‐Octadienol as Bulk Feedstock in Three Tandem Catalytic Steps
inferred← citeshttps://doi.org/10.1002/chem.201504051openalex-snapshot
In Situ FTIR and NMR Spectroscopic Investigations on Ruthenium‐Based Catalysts for Alkene Hydroformylation
inferred← citeshttps://doi.org/10.1002/chem.201705381openalex-snapshot
From Carboxytelomerization of 1,3‐Butadiene to Linear α,ω‐C10‐Diester Combinatoric Approaches for an Efficient Synthetic Route
inferred← citeshttps://doi.org/10.1002/chem.201902402openalex-snapshot
Design of a Highly Active Pd Catalyst with P,N Hemilabile Ligands for Alkoxycarbonylation of Alkynes and Allenes: A Density Functional Theory Study
inferred← citeshttps://doi.org/10.1002/chem.202100709openalex-snapshot
Oxidative Coordination versus C3−C(O)Me Bond Cleavage in Acetylacetonate Iridium Complexes
inferred← citeshttps://doi.org/10.1002/chem.202404091openalex-snapshot
Ligand‐Controlled Regioselective Alkoxycarbonylation of Nonfunctionalized Unsymmetric Internal Alkynes
inferred← citeshttps://doi.org/10.1002/chem.202404113openalex-snapshot
Carbon Monoxide and Alkoxycarbonyl Radical Enabled Migration Strategy for the Carbonylative Functionalization of Unactivated Alkenes
inferred← citeshttps://doi.org/10.1002/chem.202500476openalex-snapshot
Palladium‐Catalyzed Ethylene Methoxycarbonylation Using Bidentate Phosphines: How the Stereochemistry of the Ligand Affects the Catalyst's Activity
inferred← citeshttps://doi.org/10.1002/chem.71170openalex-snapshot
Pd‐Catalyzed Hydroalkoxycarbonylation and Hydroxycarbonylation: DFT Mapping of Catalyst‐Substrate Landscape for Product Selectivity
inferred← citeshttps://doi.org/10.1002/chin.200203281openalex-snapshot
ChemInform Abstract: Palladium‐Catalyzed Reppe Carbonylation
inferred← citeshttps://doi.org/10.1002/cite.201500096openalex-snapshot
Katalysatorvergleich bei der Hydroesterifizierung von 10‐Undecensäuremethylester in thermomorphen Lösungsmittelsystemen
inferred← citeshttps://doi.org/10.1002/cjoc.202300691openalex-snapshot
Pd‐Catalyzed Highly Regioselective Hydroesterification of Terminal Alkyl Olefins with Formates
inferred← citeshttps://doi.org/10.1002/cphc.202500360openalex-snapshot
Unraveling the Mechanism of Ligand‐Regulated Palladium‐Catalyzed Regioselective Hydrocarboxylation of Propylene with Formic Acid
inferred← citeshttps://doi.org/10.1002/cssc.201200759openalex-snapshot
A Unique Palladium Catalyst for Efficient and Selective Alkoxycarbonylation of Olefins with Formates
inferred← citeshttps://doi.org/10.1002/cssc.201402584openalex-snapshot
Synthesis of 1,4:3,6‐Dianhydrohexitols Diesters from the Palladium‐Catalyzed Hydroesterification Reaction
inferred← citeshttps://doi.org/10.1002/cssc.201403397openalex-snapshot
Biphasic Palladium‐Catalyzed Hydroesterification in a Polyol Phase: Selective Synthesis of Derived Monoesters
inferred← citeshttps://doi.org/10.1002/cssc.201600660openalex-snapshot
Multifunctional Single‐Site Catalysts for Alkoxycarbonylation of Terminal Alkynes
inferred← citeshttps://doi.org/10.1002/cssc.201800902openalex-snapshot
Integration of CO2 Reduction with Subsequent Carbonylation: Towards Extending Chemical Utilization of CO2
inferred← citeshttps://doi.org/10.1002/cssc.201802017openalex-snapshot
The Palladium‐Catalyzed Carbonylative Telomerization Reaction with Phenols, Polyphenols and Kraft Lignin
inferred← citeshttps://doi.org/10.1002/cssc.201900381openalex-snapshot
The Palladium‐Catalyzed Carboxytelomerization of Butadiene with Agrobased Alcohols and Polyols
inferred← citeshttps://doi.org/10.1002/ejic.200800282openalex-snapshot
Hydrocarboxylation of Terminal Alkenes in Supercritical Carbon Dioxide
inferred← citeshttps://doi.org/10.1002/ejic.202200037openalex-snapshot
Tandem Pauson‐Khand Reaction Using Carbon Dioxide as the C1‐Source
inferred← citeshttps://doi.org/10.1002/ejlt.202200126openalex-snapshot
Pushing Boundaries—Selective Cooling Crystallization as Tool for Selectivity Compensation and Product Purification Using a Recyclable Pd/Xantphos Catalyst in the Methoxycarbonylation of Methyl 10‐Undecenoate
inferred← citeshttps://doi.org/10.1002/ejoc.200800747openalex-snapshot
Palladium‐Catalyzed Cyclization/Carbonylation as a Direct Route to 4‐[(Methoxycarbonyl)methyl]‐3,4‐dihydroisoquinolinones
inferred← citeshttps://doi.org/10.1002/ejoc.201901601openalex-snapshot
Pd‐Catalyzed Regioselective Hydroesterification of Olefins with 2,2,2‐Trifluoroethyl Formate
inferred← citeshttps://doi.org/10.1002/ejoc.201901689openalex-snapshot
Copper(I) Catalyzed Differential Peroxidation of Terminal and Internal Alkenes Using TBHP
inferred← citeshttps://doi.org/10.1002/ejoc.202101020openalex-snapshot
Palladium‐Catalyzed Hydroformylation of Alkenes and Alkynes
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.202401010openalex-snapshot
Strong Acid‐Free Homogeneous Catalytic Systems for the Ester Products Synthesis by Alkenes Alkoxycarbonylation: Recent Advances
inferred← citeshttps://doi.org/10.1002/ejoc.202600005openalex-snapshot
Palladium‐Catalyzed Transfer Hydrocarbonylation of Alkenes and Alkynes with Formic Acid Derivatives
inferred← citeshttps://doi.org/10.1002/kin.21250openalex-snapshot
Kinetic models of the cyclohexene hydromethoxycarbonylation catalyzed by the Pd(OAc)2/trans‐2,3‐bis(diphenylphosphinomethyl)norbornane/p‐toluensulfonic acid
inferred← citeshttps://doi.org/10.1002/slct.202003395openalex-snapshot
Recent Advances in Metal‐Catalyzed Carbonylation Reactions by Using Formic Acid as CO Surrogate
inferred← citeshttps://doi.org/10.1002/slct.202401825openalex-snapshot
A Review of Synthetic Application of Homogeneous, Heterogenised‐Homogeneous, and Microwave‐Assisted Catalytic Carbonylation of Selected Substrates
inferred← citeshttps://doi.org/10.1002/tcr.20046openalex-snapshot
Unsymmetric bidentate ligands in metal‐catalyzed carbonylation of alkenes
inferred← citeshttps://doi.org/10.1002/tcr.202500071openalex-snapshot
Advances in Transition Metal‐Catalyzed Carbonylation Reactions for α,β‐Unsaturated Carbonyls: Applications, Challenges, and Opportunities
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/10.1007/3418_2018_24openalex-snapshot
Catalytic Processes Combining CO2 and Alkenes into Value-Added Chemicals
inferred← citeshttps://doi.org/10.1007/978-1-4419-9266-6_2openalex-snapshot
Palladium-Catalysed Synthesis of Mono-Esters, -Ketones and — Aldehydes/Alcohols
inferred← citeshttps://doi.org/10.1007/978-3-642-28288-1_3openalex-snapshot
Hydroformylation and Related Reactions of Renewable Resources
inferred← citeshttps://doi.org/10.1007/s10562-007-9356-6openalex-snapshot
Hydroesterification of 1-alkenes in Supercritical Carbon dioxide
inferred← citeshttps://doi.org/10.1007/s10562-008-9589-zopenalex-snapshot
Carbonylation of Naphtha by a Rhodium Complex Immobilized on Poly(4-vinylpyridine)
inferred← citeshttps://doi.org/10.1007/s10562-008-9789-6openalex-snapshot
The Nickel and Copper-Catalyzed Hydroformylation of Acetylene with Carbon Monoxide to Acrylic Acid
inferred← citeshttps://doi.org/10.1007/s10562-009-0007-yopenalex-snapshot
Promoting Effect of Lewis Acid on the Olefin Hydroesterification Catalyzed by Triphenylphosphine–Palladium Complex
inferred← citeshttps://doi.org/10.1007/s10562-009-0020-1openalex-snapshot
Methoxycarbonylation of Styrene Catalyzed by Palladium Complexes with Ferrocene Derivatives Containing Nitrogen and Phosphine Ligands
inferred← citeshttps://doi.org/10.1007/s10562-009-9930-1openalex-snapshot
Hydroformylation of Hex-1-ene by a Dinuclear gem-Dithiolato-bridged Rhodium Catalyst Under CO/H2O Conditions
inferred← citeshttps://doi.org/10.1007/s10562-011-0641-zopenalex-snapshot
Kinetics and Mechanisms of Homogeneous Catalytic Reactions. Part 11. Regioselective Hydrogenation of Quinoline Catalyzed by Rhodium Systems Containing 1,2-Bis(diphenylphosphino)ethane
inferred← citeshttps://doi.org/10.1007/s10562-014-1335-0openalex-snapshot
Kinetics and Mechanisms of Homogeneous Catalytic Reactions. Part 12. Hydroalcoxycarbonylation of 1-Hexene Using Palladium/Triphenylphosphine Systems as Catalyst Precursors
inferred← citeshttps://doi.org/10.1007/s10562-015-1502-yopenalex-snapshot
Methoxycarbonylation of Styrene Using a New Type of Palladium Complexes Bearing P,N-donor Ligands as Catalysts
inferred← citeshttps://doi.org/10.1007/s11144-015-0888-2openalex-snapshot
Kinetic aspects of the influence of concentrations of methanol and the trans-2,3-bis(diphenylphosphinomethyl)norbornane promoting additive on the hydrocarbomethoxylation of cyclohexene catalyzed by the Pd(OAc)2/p-toluenesulfonic acid system
inferred← citeshttps://doi.org/10.1007/s11144-016-1048-zopenalex-snapshot
Kinetic aspects of the influence of CO pressure on cyclohexene hydrocarbomethoxylation catalyzed by a diphosphine palladium system. Thermodynamic characteristics of some ligand exchange reactions
inferred← citeshttps://doi.org/10.1007/s11144-017-1238-3openalex-snapshot
Cyclohexene hydrocarbomethoxylation catalyzed by ruthenium(III) chloride
inferred← citeshttps://doi.org/10.1007/s11144-018-1434-9openalex-snapshot
Kinetic equations and models of cyclohexene hydrocarbomethoxylation catalyzed by the RuCl3 and RuCl3/NaCl system
inferred← citeshttps://doi.org/10.1007/s11172-014-0518-6openalex-snapshot
Effect of temperature and CO pressure on the rate of cyclohexene hydrocarbomethoxylation catalyzed by the Pd(OAc)2-PPh3-TsOH system
inferred← citeshttps://doi.org/10.1007/s11172-019-2451-1openalex-snapshot
Kinetic model for cyclohexene hydromethoxycarbonylation catalyzed by RuCl3
inferred← citeshttps://doi.org/10.1007/s11172-020-2935-zopenalex-snapshot
Model of selectivity to methyl pelargonate in hydrocarbomethoxylation of 1-octene in the presence of the Pd(PPh3)2Cl2—PPh3—p-toluenesulfonic acid catalytic system
inferred← citeshttps://doi.org/10.1007/s11172-023-3980-1openalex-snapshot
One-pot process involving dehydration of cyclohexanol and alkoxycarbonylation of cyclohexene in the presence of catalytic system PdCl2-PPh3-p-toluenesulfonic acid
inferred← citeshttps://doi.org/10.1007/s11172-024-4235-5openalex-snapshot
Highly selective Pd-catalyzed hydroxycarbonylation of styrene
inferred← citeshttps://doi.org/10.1007/s11243-018-0222-8openalex-snapshot
Tuning the regioselectivity of (benzimidazolylmethyl)amine palladium(II) complexes in the methoxycarbonylation of hexenes and octenes
inferred← citeshttps://doi.org/10.1007/s11426-021-1165-6openalex-snapshot
Palladium-catalyzed enantioselective carbonylation reactions
inferred← citeshttps://doi.org/10.1007/s11426-022-1538-8openalex-snapshot
Palladium-catalyzed 3,4-hydroaminocarbonylation of conjugated dienes for formation of β,γ-unsaturated amides
inferred← citeshttps://doi.org/10.1007/s11426-024-2535-yopenalex-snapshot
Rh-catalyzed double carbonylation of cyclopropenes toward valerolactone derivatives via cleavage of carbon–carbon double bonds
inferred← citeshttps://doi.org/10.1007/s11814-012-0073-5openalex-snapshot
A highly efficient catalyst for direct synthesis of methyl acrylate via methoxycarbonylation of acetylene
inferred← citeshttps://doi.org/10.1007/s11814-013-0026-7openalex-snapshot
Separative capability of γ-Al2O3 porous ceramic membrane modified by ZIF-8
inferred← citeshttps://doi.org/10.1007/s13738-015-0750-5openalex-snapshot
Toward the development of efficient and stable Pd-catalysts for the methoxycarbonylation of medium chain alkenes
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00424-9openalex-snapshot
4.18 Hydroformylation and Related Carbonylation Reactions of Alkenes, Alkynes, and Allenes
inferred← citeshttps://doi.org/10.1016/b978-0-08-097774-4.00601-xopenalex-snapshot
Carbonylation Reactions
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