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A Waste‐Minimized Approach to Cassar‐Heck Reaction Based on POLITAG‐Pd0 Heterogeneous Catalyst and Recoverable Acetonitrile Azeotrope
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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The Art of Meeting Palladium Specifications in Active Pharmaceutical Ingredients Produced by Pd‐Catalyzed Reactions
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Recent Applications of Palladium‐Catalyzed Coupling Reactions in the Pharmaceutical, Agrochemical, and Fine Chemical Industries
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“Click” Dendrimer‐Stabilized Palladium Nanoparticles as a Green Catalyst Down to Parts per Million for Efficient CC Cross‐Coupling Reactions and Reduction of 4‐Nitrophenol
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HandaPhos: A General Ligand Enabling Sustainable ppm Levels of Palladium‐Catalyzed Cross‐Couplings in Water at Room Temperature
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Copper‐ and phosphine‐free Sonogashira coupling reaction catalyzed by silica–(acac)‐supported palladium nanoparticles in water
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Functionalization of multi‐walled carbon nanotubes by the baclofen drug to immobilize palladium nanoparticles and catalyze Sonogashira coupling reactions
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Environmental Catalysis: Present and Future
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Sustainable Ligand‐Free Heterogeneous Palladium‐Catalyzed Sonogashira Cross‐Coupling Reaction in Deep Eutectic Solvents
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Pd–Tetrahydrosalan‐Type Complexes as Catalysts for Sonogashira Couplings in Water: Efficient Greening of the Procedure
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A Multiphase Protocol for Selective Hydrogenation and Reductive Amination of Levulinic Acid with Integrated Catalyst Recovery
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Polymer‐Anchored Bifunctional Pincer Catalysts for Chemoselective Transfer Hydrogenation and Related Reactions
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Selective Electrocatalytic Oxidation of Biomass‐Derived 5‐Hydroxymethylfurfural to 2,5‐Diformylfuran: from Mechanistic Investigations to Catalyst Recovery
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A Waste‐Minimized Approach to Cassar‐Heck Reaction Based on POLITAG‐Pd0 Heterogeneous Catalyst and Recoverable Acetonitrile Azeotrope
inferredcites →https://doi.org/10.1002/ejic.200700405openalex-snapshot
Ultra‐Low Catalyst Loading as a Concept in Economical and Sustainable Modern Chemistry: The Contribution of Ferrocenylpolyphosphane Ligands
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Pd Nanoparticles Immobilized on Nanosilica Triazine Dendritic Polymer: A Reusable Catalyst for the Synthesis of Mono‐, Di‐, and Trialkynylaromatics by Sonogashira Cross‐Coupling in Water
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Green Shades in Organic Synthesis
inferredcites →https://doi.org/10.1016/j.apcata.2013.01.021openalex-snapshot
Silica-supported PEI capped nanopalladium as potential catalyst in Suzuki, Heck and Sonogashira coupling reactions
inferredcites →https://doi.org/10.1016/j.eurpolymj.2015.10.002openalex-snapshot
Novel cross-linked polystyrenes with large space network as tailor-made catalyst supports for sustainable media
inferredcites →https://doi.org/10.1016/j.jcat.2015.06.001openalex-snapshot
Application of palladium complexes bearing acyclic amino(hydrazido)carbene ligands as catalysts for copper-free Sonogashira cross-coupling
inferredcites →https://doi.org/10.1016/j.tet.2016.03.085openalex-snapshot
Agarose functionalized phosphorus ligand for stabilization of small-sized palladium and copper nanoparticles: efficient heterogeneous catalyst for Sonogashira reaction
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Synthesis of aryl- and vinyl-substituted acetylene derivatives by the use of nickel and palladium complexes
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Palladium catalyzed synthesis of aryl, heterocyclic and vinylic acetylene derivatives
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A convenient synthesis of acetylenes: catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines
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Toward Active-Site Tailoring in Heterogeneous Catalysis by Atomically Precise Metal Nanoclusters with Crystallographic Structures
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Gram-Scale Preparation of Pd@PANI: A Practical Catalyst Reagent for Copper-Free and Ligand-Free Sonogashira Couplings
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Fast Heck–Cassar–Sonogashira (HCS) Reactions in Green Solvents
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Four-Step Total Synthesis of Selaginpulvilin D
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Sustainable HandaPhos- ppm Palladium Technology for Copper-Free Sonogashira Couplings in Water under Mild Conditions
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Zeolite-Enhanced Sustainable Pd-Catalyzed C–C Cross-Coupling Reaction: Controlled Release and Capture of Palladium
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Sonogashira Couplings Catalyzed by Fe Nanoparticles Containing ppm Levels of Reusable Pd, under Mild Aqueous Micellar Conditions
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Polarclean/Water as a Safe and Recoverable Medium for Selective C2-Arylation of Indoles Catalyzed by Pd/C
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Extensive Screening of Green Solvents for Safe and Sustainable UiO-66 Synthesis
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Sustainable Approach to Waste-Minimized Sonogashira Cross-Coupling Reaction Based on Recoverable/Reusable Heterogeneous Catalytic/Base System and Acetonitrile Azeotrope
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Ligand Free Heterogeneous Sonogashira Cross-Coupling Reaction over an in Situ Organoiodine Capsulized Palladium Anchored to a Perovskite Catalyst
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Polymer-Supported Bis-1,2,4-triazolium Ionic Tag Framework for an Efficient Pd(0) Catalytic System in Biomass Derived γ-Valerolactone
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Metal Nanoparticles Catalyzed C–C Bond Formation via C–H Activation
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Chemicals from Alkynes with Palladium Catalysts
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Unconventional Fragment Usage Enables a Concise Total Synthesis of (−)-Callyspongiolide
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Process Research and Development of a Dihydropyrimidine Dehydrogenase Inactivator: Large-Scale Preparation of Eniluracil Using a Sonogashira Coupling
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Using the Right Green Yardstick: Why Process Mass Intensity Is Used in the Pharmaceutical Industry To Drive More Sustainable Processes
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E factors, green chemistry and catalysis: an odyssey
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Recent advances in Sonogashira reactions
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Sonogashira coupling in natural product synthesis
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γ-Valerolactone as an alternative biomass-derived medium for the Sonogashira reaction
inferredcites →https://doi.org/10.1039/c4gc02175dopenalex-snapshot
Pd embedded in chitosan microspheres as tunable soft-materials for Sonogashira cross-coupling in water–ethanol mixture
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Palladium nanoparticles supported on natural nanozeolite clinoptilolite as a catalyst for ligand and copper-free C–C and C–O cross coupling reactions in aqueous medium
inferredcites →https://doi.org/10.1039/c5ra21140aopenalex-snapshot
Synthesis, characterization and catalytic activity of novel large network polystyrene-immobilized organic bases
inferredcites →https://doi.org/10.1039/c6ra17914bopenalex-snapshot
Synthesis and characterization of functionalized titania-supported Pd catalyst deriving from new orthopalladated complex of benzophenone imine: catalytic activity in the copper-free Sonogashira cross-coupling reactions at low palladium loadings
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A tailored polymeric cationic tag–anionic Pd( ii ) complex as a catalyst for the low-leaching Heck–Mizoroki coupling in flow and in biomass-derived GVL
inferredcites →https://doi.org/10.1039/c8gc04016hopenalex-snapshot
Eucalyptol: a new solvent for the synthesis of heterocycles containing oxygen, sulfur and nitrogen
inferredcites →https://doi.org/10.1039/c8sc05618hopenalex-snapshot
ppm Pd-catalyzed, Cu-free Sonogashira couplings in water using commercially available catalyst precursors
inferredcites →https://doi.org/10.1039/c9gc02546dopenalex-snapshot
“Water soluble” palladium nanoparticle engineering for C–C coupling, reduction and cyclization catalysis
inferredcites →https://doi.org/10.1039/c9gc02961copenalex-snapshot
Waste minimized synthesis of pharmaceutically active compounds via heterogeneous manganese catalysed C–H oxidation in flow
inferredcites →https://doi.org/10.1039/c9sc05947dopenalex-snapshot
Promoting heterogeneous catalysis beyond catalyst design
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Replacement strategies for non-green dipolar aprotic solvents
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A heterogeneous and recoverable palladium catalyst to access the regioselective C–H alkenylation of quinoline N -oxides
inferredcites →https://doi.org/10.3390/catal10020192openalex-snapshot
Highly Crystallized Pd/Cu Nanoparticles on Activated Carbon: An Efficient Heterogeneous Catalyst for Sonogashira Cross-Coupling Reaction
inferredcites →https://doi.org/10.3390/catal8050202openalex-snapshot
Solid-Supported Palladium Catalysts in Sonogashira Reactions: Recent Developments
inferredcites →https://doi.org/10.3390/molecules25225264openalex-snapshot
Azeotropes as Powerful Tool for Waste Minimization in Industry and Chemical Processes
inferredcites →https://doi.org/10.3762/bjoc.15.284openalex-snapshot
Palladium-catalyzed Sonogashira coupling reactions in γ-valerolactone-based ionic liquids
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Macroreticular Pincer Type Politag-20-Pd(0) as Selective Catalyst for Green Hydrogen Production from Formic Acid
inferred← citeshttps://doi.org/10.2139/ssrn.4799131openalex-extracted
Hydrogen from the Selective Dehydrogenation of Formic Acid Using Tailor-Made Bis-Imidazolium Pd(0) Based Supported Catalyst
inferred← citeshttps://doi.org/10.1016/j.cattod.2022.07.001openalex-snapshot
Macroreticular POLITAG-Pd(0) for the waste minimized hydrogenation/reductive amination of phenols using formic acid as hydrogen source
inferred← citeshttps://doi.org/10.1016/j.cattod.2022.08.018openalex-snapshot
Glycerol valorization: Development of selective protocols for acetals production through tailor-made macroreticular acid resins
inferred← citeshttps://doi.org/10.1016/j.gresc.2023.01.004openalex-snapshot
Waste-minimized continuous flow copper-catalyzed azide-alkyne cycloaddition with low metal contamination
inferred← citeshttps://doi.org/10.1016/j.gresc.2023.02.004openalex-snapshot
Waste-minimized C(sp3)-H activation for the preparation of fused N-heterocycles
inferred← citeshttps://doi.org/10.1016/j.gresc.2025.06.011openalex-snapshot
A greener approach to Buchwald-Hartwig coupling. A sustainable Pd/C-catalyzed Csp–N bond formation under microwave irradiation and bio-based solvent
inferred← citeshttps://doi.org/10.1016/j.mcat.2023.113246openalex-snapshot
Waste-minimized, solvent-free and continuous flow synthesis of α-ketoamides from aryl methyl ketones using recyclable CuBr2 catalyst, via bromo intermediate
inferred← citeshttps://doi.org/10.1016/j.mcat.2024.114235openalex-snapshot
Bis-imidazolium Pd(0) based supported catalyst for the selective dehydrogenation of formic acid
inferred← citeshttps://doi.org/10.1021/acssuschemeng.2c00550openalex-snapshot
Waste-Minimized Continuous-Flow Synthesis of Oxindoles Exploiting a Polymer-Supported N Heterocyclic Palladium Carbene Complex in a CPME/Water Azeotrope
inferred← citeshttps://doi.org/10.1021/acssuschemeng.2c03848openalex-snapshot
Tailor-Made POLITAG-Pd0 Catalyst for the Low-Loading Mizoroki–Heck Reaction in γ-Valerolactone as a Safe Reaction Medium
inferred← citeshttps://doi.org/10.1021/acssuschemeng.2c07213openalex-snapshot
POLITAG-M-F as Heterogeneous Organocatalyst for the Waste-Minimized Synthesis of β-Azido Carbonyl Compounds in Batch and under Flow Conditions
inferred← citeshttps://doi.org/10.1039/d2gc04672eopenalex-snapshot
Continuous flow synthesis of 1,4-disubstituted 1,2,3-triazoles via consecutive β-azidation of α,β-unsaturated carbonyl compounds and CuAAC reactions
inferred← citeshttps://doi.org/10.1039/d3gc01896bopenalex-snapshot
The sustainability impact of Nobel Prize Chemistry: life cycle assessment of C–C cross-coupling reactions
inferred← citeshttps://doi.org/10.1039/d3gc02516kopenalex-snapshot
Classic vs. C–H functionalization strategies in the synthesis of APIs: a sustainability comparison
inferred← citeshttps://doi.org/10.1039/d4gc00497copenalex-snapshot
Microwave assisted batch and continuous flow Suzuki–Miyaura reactions in GVL using a Pd/PiNe biowaste-derived heterogeneous catalyst
inferred← citeshttps://doi.org/10.1039/d4gc04847dopenalex-snapshot
A waste-minimized protocol for electrochemical reductive amination and its environmental assessment
inferred← citeshttps://doi.org/10.1039/d5gc06815kopenalex-snapshot
A combined microwave/continuous flow approach for the iodination of anilines and consecutive Mizoroki–Heck cross-coupling
inferred← citeshttps://doi.org/10.1039/d5sc02923fopenalex-snapshot
A new P3N ligand for Pd-catalyzed cross-couplings in water
inferred← citeshttps://doi.org/10.3390/catal11111266openalex-snapshot
Recent Progress of Metal Nanoparticle Catalysts for C–C Bond Forming Reactions
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