On the public citation graph

Pd/C/PPh3: A Simple and Efficient Catalyst System for Double Carbonylation Reactions

https://doi.org/10.1002/cjoc.200990101
0 signed · 45 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/anie.200604175openalex-snapshot
Accelerating Reactions with Microreactors at Elevated Temperatures and Pressures: Profiling Aminocarbonylation Reactions
inferredcites →https://doi.org/10.1002/chin.198433276openalex-snapshot
ChemInform Abstract: PALLADIUM‐PROMOTED DOUBLE‐CARBONYLATION REACTIONS. REACTIONS OF ORGANOPALLADIUM COMPOUNDS WITH CARBON MONOXIDE AND AMINES TO GIVE α‐KETO AMIDES
inferredcites →https://doi.org/10.1016/j.jorganchem.2003.08.014openalex-snapshot
Double carbonylation of aryl iodides with diethylamine catalyzed by dinuclear palladium complexes
inferredcites →https://doi.org/10.1016/s0022-328x(00)85589-8openalex-snapshot
Palladium(II)-catalyzed double carbonylation of organic halides in the presence of amines: α-Ketoamide synthesis
inferredcites →https://doi.org/10.1016/s0040-4039(00)87621-2openalex-snapshot
Catalytic double carbonylation of organohalogen compounds promoted by palladium complexes
inferredcites →https://doi.org/10.1016/s0040-4039(00)99373-0openalex-snapshot
Palladium-catalyzed double carbonylation of alkyl iodides bearing perfluoroalkyl group
inferredcites →https://doi.org/10.1016/s0040-4039(99)00596-1openalex-snapshot
Synthesis of pyridylglyoxylic acid derivatives via a palladium-catalysed double carbonylation of iodopyridines
inferredcites →https://doi.org/10.1021/ja00297a033openalex-snapshot
Palladium-catalyzed double carbonylation of aryl halides to give .alpha.-keto amides. Mechanistic studies
inferredcites →https://doi.org/10.1021/jo00235a017openalex-snapshot
Synthesis of .alpha.-keto esters via palladium-catalyzed double carbonylation
inferredcites →https://doi.org/10.1021/jo0156924openalex-snapshot
Double Carbonylation of Aryl Iodides with Primary Amines under Atmospheric Pressure Conditions Using the Pd/PPh3/DABCO/THF System
inferredcites →https://doi.org/10.1021/jo016342kopenalex-snapshot
Pd/C as a Reusable Catalyst for the Coupling Reaction of Halophenols and Arylboronic Acids in Aqueous Media
inferredcites →https://doi.org/10.1021/om00023a052openalex-snapshot
Effect of Copper and Iron Cocatalysts on the Palladium-Catalyzed Carbonylation Reaction of Iodobenzene
inferredcites →https://doi.org/10.1021/om00083a007openalex-snapshot
Palladium-promoted double-carbonylation reactions. Reactions of organopalladium compounds with carbon monoxide and amines to give .alpha.-keto amides
inferredcites →https://doi.org/10.1021/om00151a008openalex-snapshot
Mechanisms of double and single carbonylation reactions of aryl iodides catalyzed by palladium complexes to give .alpha.-keto esters and esters
inferredcites →https://doi.org/10.1021/op960035copenalex-snapshot
One-Step Synthesis of Biphenylacetic Acids via Pd/C-Catalyzed Arylation
inferredcites →https://doi.org/10.1039/b100951fopenalex-snapshot
Palladium-catalysed carbonylation of aryl halides in ionic liquid media: high catalyst stability and significant rate-enhancement in alkoxycarbonylation
inferredcites →https://doi.org/10.1039/b209103hopenalex-snapshot
Double carbonylation and beyond: systems at work and their organometallic models
inferredcites →https://doi.org/10.1039/b513450aopenalex-snapshot
One-pot Pd/C catalysed ‘domino’ HALEX and Sonogashira reactions: a ligand- and Cu-free alternative
inferredcites →https://doi.org/10.1039/b600632aopenalex-snapshot
Remarkable ligand effect on the palladium-catalyzed double carbonylation of aryl iodides
inferredcites →https://doi.org/10.1039/c39850000837openalex-snapshot
Palladium( II ) complex-catalysed formation of α-keto acids via double carbonylation of organic halides
inferredcites →https://doi.org/10.1246/bcsj.61.1251openalex-snapshot
Palladium-Catalyzed Double-Carbonylation of Alkenyl Halides with Secondary Amines To Give α-Keto Amides
inferredcites →https://doi.org/10.1246/bcsj.68.433openalex-snapshot
Palladium-Catalyzed Double and Single Carbonylation of Aryl Halides and Allylic Compounds
inferredcites →https://doi.org/10.1246/cl.1985.567openalex-snapshot
PALLADIUM-CATALYZED DOUBLE CARBONYLATION REACTIONS OF ARYL HALIDES AFFORDING α-KETO ESTERS
inferredcites →https://doi.org/10.5059/yukigoseikyokaishi.43.442openalex-snapshot
Novel double-carbonylation reactions of organic halides catalyzed by palladium complexes.

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4673734openalex-extracted
Triphenylphosphine-Derived Ligands for Rhodium-Catalyzed High Olefin Hydroformylations: From Traditional Molecules to Modern Cage Ligands
inferred← citeshttps://doi.org/10.1002/chin.200936076openalex-snapshot
ChemInform Abstract: Pd/C/PPh3: A Simple and Efficient Catalyst System for Double Carbonylation Reactions.
inferred← citeshttps://doi.org/10.1002/cjoc.201300675openalex-snapshot
Palladacycle‐Catalyzed Carbonylation of Aryl Iodides or Bromides with Aryl Formates
inferred← citeshttps://doi.org/10.1002/tcr.202500008openalex-snapshot
Recent Advances in the Catalytic Synthesis of α ‐Ketoamides
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2018.12.008openalex-snapshot
Polymer supported triazine based palladium complex catalyzed double carbonylation reaction of halo aryl compounds for the synthesis of α-ketoamides
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2020.121287openalex-snapshot
Double carbonylation of iodoarenes in the presence of a pyridinium SILP-Pd catalyst
inferred← citeshttps://doi.org/10.1016/j.mcat.2017.11.024openalex-snapshot
Double carbonylation of iodoarenes in the presence of reusable palladium catalysts immobilised on supported phosphonium ionic liquid phases
inferred← citeshttps://doi.org/10.1016/j.molcata.2013.06.002openalex-snapshot
Phosphine-free double carbonylation of iodobenzene in the presence of reusable supported palladium catalysts
inferred← citeshttps://doi.org/10.1016/j.molcata.2014.11.008openalex-snapshot
Phosphine-free atmospheric carbonylation of aryl iodides with aniline derivatives in the presence of a reusable silica-supported palladium catalyst
inferred← citeshttps://doi.org/10.1016/j.molcata.2016.10.025openalex-snapshot
In situ generated Pd(0) nanoparticles stabilized by bis(aryl)acenaphthenequinone diimines as catalysts for aminocarbonylation reactions in water
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00443openalex-snapshot
Recent Developments in General Methodologies for the Synthesis of α-Ketoamides
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01249openalex-snapshot
Ligand-Free Pd-Catalyzed Double Carbonylation of Aryl Iodides with Amines to α-Ketoamides under Atmospheric Pressure of Carbon Monoxide and at Room Temperature
inferred← citeshttps://doi.org/10.1039/c2cy00516fopenalex-snapshot
Palladium complexes grafted onto mesoporous silica catalysed the double carbonylation of aryl iodides with amines to give α-ketoamides
inferred← citeshttps://doi.org/10.1039/c3ra46273kopenalex-snapshot
Recent developments in palladium catalysed carbonylation reactions
inferred← citeshttps://doi.org/10.1039/c4gc02469aopenalex-snapshot
Double carbonylation of aryl iodides with amines under an atmospheric pressure of carbon monoxide using sulfur-modified Au-supported palladium
inferred← citeshttps://doi.org/10.1039/c4ra05365fopenalex-snapshot
Polymer supported Pd catalyzed carbonylation of aryl bromides for the synthesis of aryl esters and amides
inferred← citeshttps://doi.org/10.1039/c4ra07554dopenalex-snapshot
Mesoporous poly-melamine-formaldehyde stabilized palladium nanoparticle (Pd@mPMF) catalyzed mono and double carbonylation of aryl halides with amines
inferred← citeshttps://doi.org/10.1039/c5cc10389dopenalex-snapshot
Covalent triazine framework-supported palladium as a ligand-free catalyst for the selective double carbonylation of aryl iodides under ambient pressure of CO
inferred← citeshttps://doi.org/10.1039/c7ra04680dopenalex-snapshot
Mono- and double carbonylation of aryl iodides with amine nucleophiles in the presence of recyclable palladium catalysts immobilised on a supported dicationic ionic liquid phase
inferred← citeshttps://doi.org/10.1039/d0ra03406aopenalex-snapshot
Palladium nanoparticles on a pyridinium supported ionic liquid phase: a recyclable and low-leaching palladium catalyst for aminocarbonylation reactions
inferred← citeshttps://doi.org/10.1039/d4dt02627fopenalex-snapshot
Modular synthesis of triphenylphosphine-derived cage ligands for rhodium-catalyzed hydroformylation applications
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.