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Tandem selective reduction of nitroarenes catalyzed by palladium nanoclusters

https://doi.org/10.1039/c9gc03957k
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What this work says

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

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Highly Chemo‐ and Regioselective Reduction of Aromatic Nitro Compounds Catalyzed by Recyclable Copper(II) as well as Cobalt(II) Phthalocyanines
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A Different Reaction Pathway for the Reduction of Aromatic Nitro Compounds on Gold Catalysts
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Efficient and Selective Room‐Temperature Gold‐Catalyzed Reduction of Nitro Compounds with CO and H2O as the Hydrogen Source
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Reduction of Nitroaromatic Compounds on Supported Gold Nanoparticles by Visible and Ultraviolet Light
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In Situ Generated Iron Oxide Nanocrystals as Efficient and Selective Catalysts for the Reduction of Nitroarenes using a Continuous Flow Method
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Gold‐Catalyzed Direct Hydrogenative Coupling of Nitroarenes To Synthesize Aromatic Azo Compounds
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Safe and Selective Nitro Group Reductions Catalyzed by Sustainable and Recyclable Fe/ppm Pd Nanoparticles in Water at Room Temperature
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Copper‐Catalyzed [2+2+2] Modular Synthesis of Multisubstituted Pyridines: Alkenylation of Nitriles with Vinyliodonium Salts
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A Convenient and General Ruthenium‐Catalyzed Transfer Hydrogenation of Nitro‐ and Azobenzenes
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Controllable Synthesis of Mesoporous Iron Oxide Nanoparticle Assemblies for Chemoselective Catalytic Reduction of Nitroarenes
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Synthesis of Monodisperse Palladium Nanoclusters Using Metal–Organic Frameworks as Sacrificial Templates
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Pharmacological and Predicted Activities of Natural Azo Compounds
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The Nitro Group
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Room temperature selective reduction of nitrobenzene to azoxybenzene over magnetically separable urchin-like Ni/Graphene nanocomposites
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Peculiar hydrogenation reactivity of Ni–Niδ+ clusters stabilized by ceria in reducing nitrobenzene to azoxybenzene
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Modulating the catalytic behavior of non-noble metal nanoparticles by inter-particle interaction for chemoselective hydrogenation of nitroarenes into corresponding azoxy or azo compounds
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Catalytic syntheses of aromatic amines
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MeOTf- and TBD-Mediated Carbonylation of ortho-Arylanilines with CO2 Leading to Phenanthridinones
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Copper-Promoted Tandem Reaction of Azobenzenes with Allyl Bromides via N═N Bond Cleavage for the Regioselective Synthesis of Quinolines
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A Versatile Approach to the Synthesis of Functionalized Thiol-Protected Palladium Nanoparticles
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Hydroamination: Direct Addition of Amines to Alkenes and Alkynes
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A Review of the Selective Catalytic Reduction of Aromatic Nitro Compounds into Aromatic Amines, Isocyanates, Carbamates, and Ureas Using CO
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Mechanistic Studies of the Reduction of Nitroarenes by NaBH4 or Hydrosilanes Catalyzed by Supported Gold Nanoparticles
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Nitrogen-Doped Graphene-Activated Iron-Oxide-Based Nanocatalysts for Selective Transfer Hydrogenation of Nitroarenes
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Novel Inhibitors of B-RAF Based on a Disubstituted Pyrazine Scaffold. Generation of a Nanomolar Lead
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Preparation of Alkanethiolate-Protected Palladium Nanoparticles and Their Size Dependence on Synthetic Conditions
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Pd-Catalyzed Silicon Hydride Reductions of Aromatic and Aliphatic Nitro Groups
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A Highly Active Nano-Palladium Catalyst for the Preparation of Aromatic Azos under Mild Conditions
inferredcites →https://doi.org/10.1021/ol401185topenalex-snapshot
A Mild Chemoselective Ru-Catalyzed Reduction of Alkynes, Ketones, and Nitro Compounds
inferredcites →https://doi.org/10.1038/nchem.1645openalex-snapshot
Heterogenized cobalt oxide catalysts for nitroarene reduction by pyrolysis of molecularly defined complexes
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The MOF-driven synthesis of supported palladium clusters with catalytic activity for carbene-mediated chemistry
inferredcites →https://doi.org/10.1038/s41467-017-02527-8openalex-snapshot
Light-tuned selective photosynthesis of azo- and azoxy-aromatics using graphitic C3N4
inferredcites →https://doi.org/10.1038/s41929-019-0305-8openalex-snapshot
Highly active enzyme–metal nanohybrids synthesized in protein–polymer conjugates
inferredcites →https://doi.org/10.1039/b904672kopenalex-snapshot
Selective synthesis of N-aryl hydroxylamines by the hydrogenation of nitroaromatics using supported platinum catalysts
inferredcites →https://doi.org/10.1039/b906283aopenalex-snapshot
The selective reduction of nitroarenes to N-arylhydroxylamines using Zn in a CO2/H2O system
inferredcites →https://doi.org/10.1039/c000383bopenalex-snapshot
Highly selective conversion of nitrobenzenes using a simple reducing system combined with a trivalent indium salt and a hydrosilane
inferredcites →https://doi.org/10.1039/c1cc13728jopenalex-snapshot
Efficient and highly selective iron-catalyzed reduction of nitroarenes
inferredcites →https://doi.org/10.1039/c2cc30281kopenalex-snapshot
Highly efficient synthesis of aromatic azos catalyzed by unsupported ultra-thin Pt nanowires
inferredcites →https://doi.org/10.1039/c2gc35917kopenalex-snapshot
Gold nanoparticles stabilized on nanocrystalline magnesium oxide as an active catalyst for reduction of nitroarenes in aqueous medium at room temperature
inferredcites →https://doi.org/10.1039/c3gc40789fopenalex-snapshot
Highly efficient iron(0) nanoparticle-catalyzed hydrogenation in water in flow
inferredcites →https://doi.org/10.1039/c3gc42049copenalex-snapshot
Cobalt-modified molybdenum carbide as an efficient catalyst for chemoselective reduction of aromatic nitro compounds
inferredcites →https://doi.org/10.1039/c3ra23004jopenalex-snapshot
Catalysis by Pd nanoclusters generated in situ of high-efficiency synthesis of aromatic azo compounds from nitroaromatics under H2 atmosphere
inferredcites →https://doi.org/10.1039/c4cc09192bopenalex-snapshot
Selective conversion of nitroarenes using a carbon nanotube–ruthenium nanohybrid
inferredcites →https://doi.org/10.1039/c4cy00790eopenalex-snapshot
A study on the selective hydrogenation of nitroaromatics to N-arylhydroxylamines using a supported Pt nanoparticle catalyst
inferredcites →https://doi.org/10.1039/c5cc04476fopenalex-snapshot
In situ production of silver nanoparticles on an aldehyde-equipped conjugated porous polymer and subsequent heterogeneous reduction of aromatic nitro groups at room temperature
inferredcites →https://doi.org/10.1039/c7gc01992kopenalex-snapshot
I 2 -Mediated oxidative bicyclization of 4-pentenamines to prolinol carbamates with CO 2 incorporating oxyamination of the CC bond
inferredcites →https://doi.org/10.1039/c7mh00920hopenalex-snapshot
Untapped potential for debonding on demand: the wonderful world of azo-compounds
inferredcites →https://doi.org/10.1073/pnas.1717892115openalex-snapshot
Azo compounds as a family of organic electrode materials for alkali-ion batteries
inferredcites →https://doi.org/10.1086/424663openalex-snapshot
Primaquine Therapy for Malaria
inferredcites →https://doi.org/10.1126/science.1166401openalex-snapshot
Gold-Catalyzed Synthesis of Aromatic Azo Compounds from Anilines and Nitroaromatics
inferredcites →https://doi.org/10.1126/science.1242005openalex-snapshot
Nanoscale Fe 2 O 3 -Based Catalysts for Selective Hydrogenation of Nitroarenes to Anilines
inferredcites →https://doi.org/10.5860/choice.39-2805openalex-snapshot
The nitro group in organic synthesis

What points at this work

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

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A Concise Route to Cyclic Amines from Nitroarenes and Ketoacids under Iron‐Catalyzed Hydrosilylation Conditions
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Light‐promoted Selective Reduction of Nitroarenes to Azoxy‐, Azo‐ and Hydrazo‐compounds Catalyzed by Bismuth Porphyrin Metal Organic Framework
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Gold Nanoparticle‐Catalyzed Solvent Switchable Selective Partial Reduction of Nitrobenzene to N‐Phenylhydroxylamine and Azoxybenzene
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Electrosynthesis of Azobenzenes Directly from Nitrobenzenes
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Two-dimensional porous Cu-CuO nanosheets: Integration of heterojunction and morphology engineering to achieve high-effective and stable reduction of the aromatic nitro-compounds
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Palladium supported on copoly(ionic liquid) nanohydrogel functionalized carbon nanotubes and its catalytic performance
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Engineering of cobalt sulfide (Co5S2) microcubes for selective catalytic hydrogenation of nitroarenes and enhanced calorific value of fuel
inferred← citeshttps://doi.org/10.1016/j.cplett.2022.139431openalex-snapshot
Catalytic reduction of nitroarenes and Suzuki-Miyaura reactions using Pd complex stabilized on the functionalized polymeric support
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Fabrication of silver nanoparticles within chitosan based microgels for catalysis
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Heterogeneous synergistic catalysts enable efficient catalytic transfer hydrogenation of nitro compounds via in-situ provided hydrogen
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Highly efficient and selective partial reduction of nitroarenes to N-arylhydroxylamines catalysed by phosphine oxide-decorated polymer immobilized ionic liquid stabilized ruthenium nanoparticles
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Ruthenium nickel bimetallic nanoparticles embedded in nitrogen-doped carbon mesoporous spheres as a superior catalyst for the hydrogenation of toxic nitroarenes
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Nickel nanoprism containing ppm level of Pd catalysis of reduction and Suzuki-Miyaura reactions
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3d transition metal-based single-atom catalyst as an emerging field for environmentally benign organic transformation reactions
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Constructing a synergistic catalyst by confining Pd within a MOF using an extended “bottle-around-ship” protocol
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Direct Synthesis of Indoles from Azoarenes and Ketones with Bis(neopentylglycolato)diboron Using 4,4′-Bipyridyl as an Organocatalyst
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Convergent Paired Electrochemical Synthesis of Azoxy and Azo Compounds: An Insight into the Reaction Mechanism
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Polar hydrogen species mediated nitroarenes selective reduction to anilines over an [FeMo]S x catalyst
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Photo-induced redox cascade reaction of nitroarenes and amines
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Zirconium phosphate supported-silver nanoparticles for selective hydrogenation of nitrobenzene into azoxybenzene compounds
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Hydrosilylation and hydrogen transfer reactions promoted by molecular defined iron catalysts
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