On the public citation graph

Leaching Mechanism of Different Palladium Surface Species in Heck Reactions of Aryl Bromides and Chlorides

0 signed · 121 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/(sici)1521-3765(20000303)6:5<843::aid-chem843>3.0.co;2-gopenalex-snapshot
Heck Reactions of Iodobenzene and Methyl Acrylate with Conventional Supported Palladium Catalysts in the Presence of Organic and/or Inorganic Bases without Ligands
inferredcites →https://doi.org/10.1002/1099-0682(200105)2001:5<1131::aid-ejic1131>3.0.co;2-3openalex-snapshot
Metallic Palladium in the Heck Reaction: Active Catalyst or Convenient Precursor?
inferredcites →https://doi.org/10.1002/1521-3765(20020201)8:3<622::aid-chem622>3.0.co;2-0openalex-snapshot
Highly Active Palladium/Activated Carbon Catalysts for Heck Reactions: Correlation of Activity, Catalyst Properties, and Pd Leaching
inferredcites →https://doi.org/10.1002/9783527627097openalex-snapshot
Modern Surface Organometallic Chemistry
inferredcites →https://doi.org/10.1002/9783527648283openalex-snapshot
Palladium‐Catalyzed Coupling Reactions
inferredcites →https://doi.org/10.1002/adsc.200404119openalex-snapshot
Pd(II)‐Schiff Base Complexes Heterogenised on MCM‐41 and Delaminated Zeolites as Efficient and Recyclable Catalysts for the Heck Reaction
inferredcites →https://doi.org/10.1002/adsc.200404264openalex-snapshot
Evidence that SCS Pincer Pd(II) Complexes are only Precatalysts in Heck Catalysis and the Implications for Catalyst Recovery and Reuse
inferredcites →https://doi.org/10.1002/adsc.200505473openalex-snapshot
On the Nature of the Active Species in Palladium Catalyzed Mizoroki–Heck and Suzuki–Miyaura Couplings – Homogeneous or Heterogeneous Catalysis, A Critical Review
inferredcites →https://doi.org/10.1002/adsc.200900765openalex-snapshot
Recyclable Heterogeneous Palladium Catalysts in Pure Water: Sustainable Developments in Suzuki, Heck, Sonogashira and Tsuji–Trost Reactions
inferredcites →https://doi.org/10.1002/adsc.201000458openalex-snapshot
Macrocyclic Palladium(II) Complexes in CC Coupling Reactions: Efficient Catalysis by Controlled Temporary Release of Active Species
inferredcites →https://doi.org/10.1002/anie.200353473openalex-snapshot
In Situ Generation of Highly Active Dissolved Palladium Species from Solid Catalysts—A Concept for the Activation of Aryl Chlorides in the Heck Reaction
inferredcites →https://doi.org/10.1002/anie.200390072openalex-snapshot
Homogeneous and Heterogeneous Catalysis: Bridging the Gap through Surface Organometallic Chemistry
inferredcites →https://doi.org/10.1002/anie.201006374openalex-snapshot
From Noble Metal to Nobel Prize: Palladium‐Catalyzed Coupling Reactions as Key Methods in Organic Synthesis
inferredcites →https://doi.org/10.1002/aoc.3839openalex-snapshot
Pd‐ Dithizone grafted onto magnetic nanoparticles and study of its catalyticactivity in C‐C and C‐N coupling reactions
inferredcites →https://doi.org/10.1002/cctc.201100422openalex-snapshot
Heterogeneous versus Homogeneous Palladium Catalysts for Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/chin.200305265openalex-snapshot
Palladium‐Catalyzed Coupling Reactions.
inferredcites →https://doi.org/10.1002/ejic.200800846openalex-snapshot
Pd/MOx Materials Synthesized by Sol‐Gel Coprecipitation as Catalysts for Carbon–Carbon Coupling Reactions of Aryl Bromides and Chlorides
inferredcites →https://doi.org/10.1006/jcat.2000.2934openalex-snapshot
Recyclable Homogeneous/Heterogeneous Catalytic Systems for Heck Reaction through Reversible Transfer of Palladium Species between Solvent and Support
inferredcites →https://doi.org/10.1007/s10975-005-0101-0openalex-snapshot
Oxidative Addition Step in Reactions Involving Palladium Activation of Carbon-Halogen and Carbon-Oxygen Bonds
inferredcites →https://doi.org/10.1016/0040-4020(96)00547-9openalex-snapshot
On the efficiency of tetraalkylammonium salts in Heck type reactions
inferredcites →https://doi.org/10.1016/j.cattod.2017.10.013openalex-snapshot
Spatial, temporal and quantitative assessment of catalyst leaching in continuous flow
inferredcites →https://doi.org/10.1016/j.ccr.2009.06.001openalex-snapshot
Silica-supported palladium: Sustainable catalysts for cross-coupling reactions
inferredcites →https://doi.org/10.1016/j.ccr.2016.12.021openalex-snapshot
Understanding active species in catalytic transformations: From molecular catalysis to nanoparticles, leaching, “Cocktails” of catalysts and dynamic systems
inferredcites →https://doi.org/10.1016/j.cej.2019.05.197openalex-snapshot
Pd nanoparticle and molecular Pd2+ leaching pathways for a strongly acid versus strongly basic resin supported Pd nanoparticle catalyst in Suzuki coupling
inferredcites →https://doi.org/10.1016/j.jcat.2004.05.015openalex-snapshot
Silica and polymer-tethered Pd?SCS-pincer complexes: evidence for precatalyst decomposition to form soluble catalytic species in Mizoroki?Heck chemistry
inferredcites →https://doi.org/10.1016/j.jcat.2004.06.026openalex-snapshot
Synthesis and characterization of carbometallated palladacycles over 3-hydroxypropyltriethoxysilyl-functionalized MCM-41
inferredcites →https://doi.org/10.1016/j.jcat.2007.07.005openalex-snapshot
Strong evidence of solution-phase catalysis associated with palladium leaching from immobilized thiols during Heck and Suzuki coupling of aryl iodides, bromides, and chlorides
inferredcites →https://doi.org/10.1016/j.jcat.2018.09.014openalex-snapshot
A new efficient, highly dispersed, Pd nanoparticulate silica supported catalyst synthesized from an organometallic precursor. Study of the homogeneous vs. heterogeneous activity in the Suzuki-Miyaura reaction
inferredcites →https://doi.org/10.1016/j.jcat.2019.06.004openalex-snapshot
Synthesis of methyl palladium complexes on silica as single site catalysts activating C Cl bonds in heck reactions
inferredcites →https://doi.org/10.1016/j.tet.2005.06.111openalex-snapshot
Design of highly active heterogeneous palladium catalysts for the activation of aryl chlorides in Heck reactions
inferredcites →https://doi.org/10.1016/s0040-4039(00)70335-2openalex-snapshot
Noble metal hydroxides on carbon nonpyrophoric dry catalysts
inferredcites →https://doi.org/10.1016/s0040-4039(97)01286-0openalex-snapshot
Automated synthesis of double dye-labeled oligonucleotides using tetramethylrhodamine (TAMRA) solid supports
inferredcites →https://doi.org/10.1016/s0040-4039(98)01135-6openalex-snapshot
[Pd/Base/QX] catalyst systems for directing Heck-type reactions
inferredcites →https://doi.org/10.1016/s1381-1169(03)00382-0openalex-snapshot
Simple method for enhancement of the ligand-free palladium catalyst activity in the Heck reaction with non-activated bromoarenes
inferredcites →https://doi.org/10.1016/s1381-1169(99)00369-6openalex-snapshot
Palladium-catalyzed homogeneous and heterogeneous Heck reactions in NMP and water-mixed solvents using organic, inorganic and mixed bases
inferredcites →https://doi.org/10.1021/acs.chemrev.5b00373openalex-snapshot
Surface Organometallic and Coordination Chemistry toward Single-Site Heterogeneous Catalysts: Strategies, Methods, Structures, and Activities
inferredcites →https://doi.org/10.1021/acs.chemrev.7b00443openalex-snapshot
Pd Metal Catalysts for Cross-Couplings and Related Reactions in the 21st Century: A Critical Review
inferredcites →https://doi.org/10.1021/acs.organomet.7b00184openalex-snapshot
A New Mode of Operation of Pd-NHC Systems Studied in a Catalytic Mizoroki–Heck Reaction
inferredcites →https://doi.org/10.1021/acscatal.9b00207openalex-snapshot
Modeling Key Pathways Proposed for the Formation and Evolution of “Cocktail”-Type Systems in Pd-Catalyzed Reactions Involving ArX Reagents
inferredcites →https://doi.org/10.1021/cr100355bopenalex-snapshot
Efficient, Selective, and Recyclable Palladium Catalysts in Carbon−Carbon Coupling Reactions
inferredcites →https://doi.org/10.1021/cr9903048openalex-snapshot
The Heck Reaction as a Sharpening Stone of Palladium Catalysis
inferredcites →https://doi.org/10.1021/ic061898hopenalex-snapshot
Mizoroki−Heck Coupling Using Immobilized Molecular Precatalysts: Leaching Active Species from Pd Pincers, Entrapped Pd Salts, and Pd NHC Complexes
inferredcites →https://doi.org/10.1021/ic061907mopenalex-snapshot
Genesis of Coordinatively Unsaturated Palladium Complexes Dissolved from Solid Precursors during Heck Coupling Reactions and Their Role as Catalytically Active Species
inferredcites →https://doi.org/10.1021/jo00409a001openalex-snapshot
Palladium-catalyzed vinylic substitution with highly activated aryl halides
inferredcites →https://doi.org/10.1021/om00114a028openalex-snapshot
Dimethyl(N,N,N',N'-tetramethylethanediamine)palladium(II) and dimethyl[1,2-bis(dimethylphosphino)ethane]palladium(II): syntheses, x-ray crystal structures, and thermolysis, oxidative-addition and ligand-exchange reactions
inferredcites →https://doi.org/10.1021/om201120nopenalex-snapshot
Toward the Ideal Catalyst: From Atomic Centers to a “Cocktail” of Catalysts
inferredcites →https://doi.org/10.1039/b316553copenalex-snapshot
Solid-supported cross-coupling catalysts derived from homogeneous nickel and palladium coordination complexesElectronic supplementary information (ESI) available: Synthesis of the complexes and crystallographic data for 1 and 2. See http://www.rsc.org/suppdata/dt/b3/b316553c/
inferredcites →https://doi.org/10.1039/b506276bopenalex-snapshot
A unifying mechanism for all high-temperature Heck reactions. The role of palladium colloids and anionic species
inferredcites →https://doi.org/10.1039/c4gc00314dopenalex-snapshot
A molecular Pd( ii ) complex incorporated into a MOF as a highly active single-site heterogeneous catalyst for C–Cl bond activation
inferredcites →https://doi.org/10.1134/s002315840703007xopenalex-snapshot
Kinetics of the Heck reactions of styrene with bromobenzene and iodobenzene in the presence of ligandless catalytic systems: A comparative study
inferredcites →https://doi.org/10.1139/cjc-78-6-920openalex-snapshot
Heck reaction using palladium complexed to dendrimers on silica
inferredcites →https://doi.org/10.3998/ark.5550190.0012.817openalex-snapshot
In situ NMR studies of the mechanism of homogeneously and heterogeneously catalysed Heck reactions of aryl chlorides and bromides

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.4719368openalex-extracted
Pd Nanocatalysts Supported on Hollow Carbon Spheres for Heck Reaction: Void-Confinement Effect with Varying Space Size in Liquid-Phase Processes
inferred← citeshttps://doi.org/10.1002/aoc.70330openalex-snapshot
Bis(Biguanide)‐Anchored Palladium on Covalent Organic Framework: Highly Stable and Recyclable Catalyst for Suzuki, Heck, and Sonogashira Reactions
inferred← citeshttps://doi.org/10.1002/aoc.70549openalex-snapshot
Enhancing Palladium Catalytic Performance Through Modification of Chitosan Nanofiber With Aldehyde Functional Groups
inferred← citeshttps://doi.org/10.1002/cctc.202001526openalex-snapshot
Oxidative Alkenylation of Arenes Using Supported Rh Materials: Evidence that Active Catalysts are Formed by Rh Leaching
inferred← citeshttps://doi.org/10.1002/cctc.202501395openalex-snapshot
Heterogenized PCP Pd Pincer Complexes for the Arylation of Styrenes With Iodonium Salts
inferred← citeshttps://doi.org/10.1002/cctc.71037openalex-snapshot
Reaction‐Field‐Dependent Selective Ullmann Coupling Versus Hydrodebromination and Heck Reaction of Aryl Bromides
inferred← citeshttps://doi.org/10.1002/chem.202302825openalex-snapshot
Support Engineering for the Stabilisation of Heterogeneous Pd3P‐Based Catalysts for Heck Coupling Reactions
inferred← citeshttps://doi.org/10.1002/cssc.202501205openalex-snapshot
Durable Heterogeneous Pd‐PNP Pincer Complex for CarbonCarbon Bond Formation in Continuous‐Flow Systems
inferred← citeshttps://doi.org/10.1002/ejoc.202200009openalex-snapshot
C−I Selective Sonogashira and Heck Coupling Reactions Catalyzed by Aromatic Triangular Tri‐palladium
inferred← citeshttps://doi.org/10.1007/s10562-021-03577-wopenalex-snapshot
Enhanced Performance of Palladium Catalyst Confined Within Carbon Nanotubes for Heck Reaction
inferred← citeshttps://doi.org/10.1007/s11172-023-3921-zopenalex-snapshot
Comparison of palladium leaching from the Pd/MWCNT catalyst in important organic synthesis reactions
inferred← citeshttps://doi.org/10.1007/s11172-023-3993-9openalex-snapshot
Theoretical and experimental investigations of the PIII/PV transition in a phosphorus-doped carbon material
inferred← citeshttps://doi.org/10.1007/s11172-024-4159-0openalex-snapshot
The role of phosphines in the activations of coupled substrates in the Suzuki—Miyaura reaction
inferred← citeshttps://doi.org/10.1016/j.apcata.2026.121035openalex-snapshot
Leaching, redistribution, and dynamic heterogeneity in supported catalysts
inferred← citeshttps://doi.org/10.1016/j.apcato.2024.206928openalex-snapshot
Pd Nanocatalysts supported on hollow carbon spheres for heck reaction: Void-confinement effect with varying space size in liquid-phase processes
inferred← citeshttps://doi.org/10.1016/j.catcom.2022.106441openalex-snapshot
Leaching of palladium atoms from small cluster models during Heck reactions – An experimental and theoretical study
inferred← citeshttps://doi.org/10.1016/j.cattod.2024.114903openalex-snapshot
Carbonylative transformations with Pd catalysts supported on bio-degradable urea-based polymer – Part A
inferred← citeshttps://doi.org/10.1016/j.ccr.2026.218426openalex-snapshot
Dynamic toxicity of metal-containing systems: Biological effects emerge from evolving metal cocktails
inferred← citeshttps://doi.org/10.1016/j.ces.2024.120554openalex-snapshot
Assessment of sulfuric acid as pH control agent in catalytic nitrate reduction in drinking waters
inferred← citeshttps://doi.org/10.1016/j.cogsc.2021.100502openalex-snapshot
Transition metal ‘cocktail’-type catalysis
inferred← citeshttps://doi.org/10.1016/j.colsurfa.2025.138554openalex-snapshot
Polydopamine-mediated anchoring of Pd on magnetic Ni@CNTs: A robust core-shell nanocatalyst for recyclable heck cross-coupling
inferred← citeshttps://doi.org/10.1016/j.cplett.2023.140542openalex-snapshot
Effect of electron transfer in Pd on nitrogen-doped carbon nanotube catalysts in the Heck reaction
inferred← citeshttps://doi.org/10.1016/j.jcat.2021.05.020openalex-snapshot
Catalytic performance of palladium nanoparticles encapsulated within nitrogen-doped carbon during Heck reaction
inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115333openalex-snapshot
Immobilization of palladium nanoparticles on polydopamine spheres with superior activity and reusability in Heck reaction
inferred← citeshttps://doi.org/10.1016/j.jcat.2026.116733openalex-snapshot
Carbonylation catalysis of aryl halides through active-site engineering
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2022.122319openalex-snapshot
Comparative assessment of heterogeneous and homogeneous Suzuki-Miyaura catalytic reactions using bio-Profiles and bio-Factors
inferred← citeshttps://doi.org/10.1016/j.mcat.2022.112260openalex-snapshot
Fast reversible oxidative addition of demanding aryl chlorides to Pd under real conditions of catalysis in the Mizoroki-Heck reaction: The kinetic proof
inferred← citeshttps://doi.org/10.1016/j.mcat.2026.116221openalex-snapshot
Annealing atmosphere-modulated Ti3+ defects in TiO2 nanotube arrays for Pd-catalyzed Heck coupling
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.139081openalex-snapshot
Study of size effect of palladium atoms as single-atom and clusters nanoparticle catalysts for Heck reactions
inferred← citeshttps://doi.org/10.1016/j.seppur.2024.127492openalex-snapshot
Leaching of palladium from spent Pd/Al2O3 catalysts by coupled ultrasound-microwave technique
inferred← citeshttps://doi.org/10.1016/s1872-2067(23)64616-9openalex-snapshot
Pd loaded TiO2 as recyclable catalyst for benzophenone synthesis by coupling benzaldehyde with iodobenzene under UV light
inferred← citeshttps://doi.org/10.1021/acs.jpcc.0c06979openalex-snapshot
High Activity and Stability of PdOx Anchored in Porous NiO Nanofibers for Catalyzing Suzuki Coupling Reactions
inferred← citeshttps://doi.org/10.1021/acs.oprd.1c00041openalex-snapshot
Heterogeneous Catalysis for Cross-Coupling Reactions: An Underutilized Powerful and Sustainable Tool in the Fine Chemical Industry?
inferred← citeshttps://doi.org/10.1021/acs.organomet.3c00308openalex-snapshot
Time-Resolved 3D Hammett Correlation to Monitor Catalyst Behavior with No Differential Data in Hand
inferred← citeshttps://doi.org/10.1021/acs.organomet.4c00255openalex-snapshot
True Homogeneous “Ligand-Free” Catalysis in Mizoroki–Heck Mono- and Double Arylations with Nonreactive Aryl Chlorides
inferred← citeshttps://doi.org/10.1021/acs.organomet.5c00117openalex-snapshot
Cocktail-Type Catalysis: An Emerging Concept in Metal-Mediated Transformations
inferred← citeshttps://doi.org/10.1021/acs.organomet.5c00198openalex-snapshot
Carbon Monoxide-Induced Mobility of Isolated Palladium Species on Silicon Dioxide at Room Temperature
inferred← citeshttps://doi.org/10.1021/acsanm.2c00389openalex-snapshot
Water-Soluble Palladium Nanoclusters as Catalysts in Ligand-Free Suzuki–Miyaura Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/acscatal.2c01749openalex-snapshot
“Hidden” Nanoscale Catalysis in Alkyne Hydrogenation with Well-Defined Molecular Pd/NHC Complexes
inferred← citeshttps://doi.org/10.1021/acscatal.3c03889openalex-snapshot
4D Catalysis Concept Enabled by Multilevel Data Collection and Machine Learning Analysis
inferred← citeshttps://doi.org/10.1021/acscatal.4c02028openalex-snapshot
Deconvoluting Substrates, Support, and Temperature Effects on Leaching and Deactivation of Pd Catalysts: An In Situ Study in Flow
inferred← citeshttps://doi.org/10.1021/acsomega.6c01810openalex-snapshot
Sustainable Mizoroki–Heck Cross-Coupling Using a Pd(II)-Polymer as Precatalyst in 1-Butanol
inferred← citeshttps://doi.org/10.1021/jacs.1c01810openalex-snapshot
Advances in Group 10 Transition-Metal-Catalyzed Arene Alkylation and Alkenylation
inferred← citeshttps://doi.org/10.1021/jacs.3c00645openalex-snapshot
Time-Resolved Formation and Operation Maps of Pd Catalysts Suggest a Key Role of Single Atom Centers in Cross-Coupling
inferred← citeshttps://doi.org/10.1038/s41467-021-22084-5openalex-snapshot
Enhancing stability by trapping palladium inside N-heterocyclic carbene-functionalized hypercrosslinked polymers for heterogeneous C-C bond formations
inferred← citeshttps://doi.org/10.1039/d0qi01133aopenalex-snapshot
Comparative study of aryl halides in Pd-mediated reactions: key factors beyond the oxidative addition step
inferred← citeshttps://doi.org/10.1039/d0qi01411gopenalex-snapshot
Different effects of metal-NHC bond cleavage on the Pd/NHC and Ni/NHC catalyzed α-arylation of ketones with aryl halides
inferred← citeshttps://doi.org/10.1039/d1cy01601fopenalex-snapshot
Evidence for “cocktail”-type catalysis in Buchwald–Hartwig reaction. A mechanistic study
inferred← citeshttps://doi.org/10.1039/d1gc02311jopenalex-snapshot
Lipids as versatile solvents for chemical synthesis
inferred← citeshttps://doi.org/10.1039/d2cy01857hopenalex-snapshot
Fiber-glass supported catalysis: real-time, high-resolution visualization of active palladium catalytic centers during the reduction of nitro compounds
inferred← citeshttps://doi.org/10.1039/d2qo01652dopenalex-snapshot
Atom-economical synthesis of 1,2-bis(phosphine oxide)ethanes from calcium carbide with straightforward access to deuterium- and 13 C-labeled bidentate phosphorus ligands and metal complexes
inferred← citeshttps://doi.org/10.1039/d3sc06447fopenalex-snapshot
Evidence for Suzuki–Miyaura cross-couplings catalyzed by ligated Pd 3 -clusters: from cradle to grave
inferred← citeshttps://doi.org/10.1039/d4ob01177eopenalex-snapshot
Palladium nanoparticle catalyzed synthesis of indoles via intramolecular Heck cyclisation
inferred← citeshttps://doi.org/10.1039/d5cc00796hopenalex-snapshot
One-pot synthesis of a highly active single-atom Pd catalyst for the Heck reaction
inferred← citeshttps://doi.org/10.1055/a-1661-3152openalex-snapshot
Suzuki–Miyaura Cross-Coupling Reaction with Potassium Aryltrifluoroborate in Pure Water Using Recyclable Nanoparticle Catalyst
inferred← citeshttps://doi.org/10.1080/00397911.2025.2481641openalex-snapshot
Palladium based ZIFs: Heterogeneous catalysts for coupling and selective hydrogenation reactions
inferred← citeshttps://doi.org/10.1080/14756366.2026.2621477openalex-snapshot
Palladium-catalysed synthesis of small-molecule epigenetic inhibitors as anticancer therapeutics
inferred← citeshttps://doi.org/10.1134/s0012500823600657openalex-snapshot
Stability of Pd/C Catalysts in Solvents for Organic Synthesis
inferred← citeshttps://doi.org/10.1134/s002315842360116xopenalex-snapshot
Visualization of the Dynamics of Catalyst Transformations Based on the Results of Competing Experiments
inferred← citeshttps://doi.org/10.1134/s0023158425600439openalex-snapshot
Approaches to the Interpretation of Machine Learning Models Trained with Big Experimental Kinetic Data: An Example of the Suzuki–Miyaura Reaction
inferred← citeshttps://doi.org/10.1134/s0023158425600440openalex-snapshot
A Study of the Kinetics of the Mizoroki–Heck Reaction on the Pd/P. yeei Catalyst
inferred← citeshttps://doi.org/10.1186/s40712-025-00289-6openalex-snapshot
A method for recycling the Pd catalyst at molar ppm level
inferred← citeshttps://doi.org/10.1515/mgmc-2020-0023openalex-snapshot
Magnetically recoverable nanostructured Pd complex of dendrimeric type ligand on the MCM-41: Preparation, characterization and catalytic activity in the Heck reaction
inferred← citeshttps://doi.org/10.1515/pac-2023-0111openalex-snapshot
The nitro to amine reduction: from millions of tons to single molecule studies
inferred← citeshttps://doi.org/10.31857/s0453881124020071openalex-snapshot
The method for the vizualization of the dynamics of catalyst transformations based on the results of competing experiments
inferred← citeshttps://doi.org/10.31857/s2686953522600726openalex-snapshot
STABILITY OF Pd/C CATALYSTS IN SOLVENTS FOR ORGANIC SYNTHESIS
inferred← citeshttps://doi.org/10.3390/nano10122457openalex-snapshot
Sterically Hindered Phosphonium Salts: Structure, Properties and Palladium Nanoparticle Stabilization
inferred← citeshttps://doi.org/10.3390/su13179862openalex-snapshot
Tri-tert-butyl(n-alkyl)phosphonium Ionic Liquids: Structure, Properties and Application as Hybrid Catalyst Nanomaterials
inferred← citeshttps://doi.org/10.59761/rcr5182openalex-snapshot
Acetylene semi-hydrogenation: recent advances
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.