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Homogeneous ruthenium-catalyzed reduction of nitrobenzene

https://doi.org/10.1021/ic50084a034
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Environmentally Safe Magnetic/Chitosan-Based Nickel Schiff Base Composite as a Heterogeneous and Magnetically Recoverable Nanocatalyst for Mild and Efficient Reduction of Nitroarenes
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Metal‐Catalyzed Reactions of Carbon Monoxide
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Metal Carbonyls Important in Catalysis
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Mechanistische Aspekte der Carbonylierung von Nitrobenzol mit Rhodiumkatalysatoren
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Katalyse mit molekularen Metall-Clustern
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Mechanistic Aspects of the Carbonylation of Nitrobenzene with Rhodium Catalysts
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Catalysis by Molecular Metal Clusters
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Metal–Organic Framework Mediated Cobalt/Nitrogen‐Doped Carbon Hybrids as Efficient and Chemoselective Catalysts for the Hydrogenation of Nitroarenes
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ChemInform Abstract: HOMOGENE DURCH RUTHENIUM KATALYSIERTE REDUKTION VON NITROBENZOL
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Hollow Nano‐Mesosilica Spheres Containing Rhodium Nanoparticles Supported on Nitrogen‐Doped Carbon: An Efficient Catalyst for the Reduction of Nitroarenes under Mild Conditions
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Catalytic deoxygenation of organic compounds by carbon monoxide: III. The reaction under pressure of aromatic nitro compounds in the presence of o‐phthalaldehyde
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Die übergangsmetall‐katalysierte reduktive Carbonylierung von Arylaziden zu 1,3‐Diarylharnstoffen
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Iron Carbonyls in Organic Synthesis, I. Iron Pentacarbonyl Induced Decomposition and Transfer Hydrogenation of Aryl Azides to Substituted Ureas
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Preparation of mono(dimethylglyoxime)(triphenylphosphine)-halogenocobalt(I) complexes and their application as homogeneous catalysts in reduction of aromatic nitrocompounds
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Homogeneous reduction of aromatic nitrocompounds by a triphenylphosphine complex of palladium
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Reduction of nitroaromatics with poly(vinylpyridine) complexes of palladium(II) and platinum(II)
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Preparation of mono(dimethylglyoxime)(triphenylphosphine)‐halogenocobalt(I) complexes and their application as homogeneous catalysts in reduction of aromatic nitrocompounds
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Homogeneous catalysis of the reduction of nitrobenzene by bromotris(triphenylphosphine) copper (I)
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Studies on the reduction of nitrobenzene to aniline catalysed by pd(acac)2‐pyridine system
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Quantenchemische Untersuchungen zur Carbonylierung von Nitrosoverbindungen, III. Der Einfluß von Metallkatalysatoren des Typs MXCOL2auf ausgewählte Ausschnitte der Potentialfläche der Carbonylierung von Nitrosomethan
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Zur Rhodium‐katalysierten Carbonylierung aromatischer Nitroverbindungen zu Isocyanaten. I. Katalysatoren und Reaktionsbedingungen
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Cobaltchelate als Hydrierkatalysatoren. Zur Reduktion von Nitro‐ zu Aminoverbindungen mit Kohlenmonoxid und Wasser als Hydriermittel
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Phosphorous‐modified Porous Carbon Supported Nickel Nanoparticles as a Catalyst for the Reduction of Nitroaromatics in Water
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Interplay of Electronic and Steric Effects of R2PH (R = tBu, o‐tolyl) in Reactions with Triruthenium Dodecacarbonyl
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Promotion Effects in Transition Metal-Catalyzed Carbonylation
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Metal Clusters in Catalysis
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Metal Catalysed Deoxygenation Reactions by Carbon Monoxide of Nitroso and Nitro Compounds
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Homogeneous Catalytic Reduction of Carbonyl-, Azomethine- and Nitro-Groups
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Synthesis of Other Non-Cyclic Compounds
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Heterogenization of palladium(II) chelates on a sibunite
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Homogeneous catalysis by ruthenium carbonyl clusters
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Carbonyl complexes as homogeneous and supported catalysts
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Molecular orbital calculations on [HRu3(CO)9(PhNCO)]− and related clusters
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Catalytic reductive carbonylation of aromatic nitro compounds to urethanes promoted by supported palladium activated with 1,10-phenanthroline derivatives
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Palladium-catalysed N,N′-disubstituted urea synthesis by oxidative carbonylation of amines under CO and O2 at atmospheric pressure
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Catalytic reduction of nitroaromatics with carbon monoxide and water using tricarbonyltetraphenylcyclopentadienone ruthenium(0)
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Catalytic reduction of nitrobenzene to aniline with aqueous methyl formate
inferred← citeshttps://doi.org/10.1016/0022-328x(95)05986-yopenalex-snapshot
Tri- and binuclear ruthenium carbonyl complexes containing bridging ligands derived from ortho-substituted anilines. A comparative study of their syntheses using RuCl3 · nH2O or [Ru3(CO)12] as starting materials
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Preface
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Homogeneous catalysis by ruthenium complexes
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Transition metal cluster complexes as catalysts. A review
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Methods of catalysis presumably similar to enzymatic XIII. Transition metal complexes analogous to hydrogenase. Hydrogenation of nitroaromatics
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Metal cluster catalysis. 2. Selective reduction of nitrobenzene catalyzed by rhodium carbonyl cluster anions. Evidence for water gas shift reaction
inferred← citeshttps://doi.org/10.1016/0304-5102(83)80066-2openalex-snapshot
Selective reduction of nitroaromatic compounds via hydrogen transfer, catalyzed by Ir(I) complexes with 2,2'-bipyridine, 1,10-phenanthroline and derivatives
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Activation of carbonyl clusters with 1,10-phenanthroline and related ligands: the reduction of nitrobenzene with Co + H2O as a model reaction for Mx(CO)y (M = Ru, Os, Ir) + phen systems as catalyst precursors
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The chemistry and catalytic properties of ruthenium and osmium complexes
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Dihydrogen reduction of nitroaromatics, alkenes, alkynes and aromatic carbonyls by ortho-metalated Pd(II) complexes in homogeneous phase
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Selective reductions of aromatic carbonyls and nitrobenzene by new interiamellar montmorillonite-suylamine-palladium(II) catalyst
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Oxidative carbonylation of aniline catalyzed by Pd(II)-2,2'-bipyridyl complex intercalated in α-zirconium-phosphate
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Formaldehyde and formates as sources of synthesis gas via ruthenium-catalyzed decomposition reactions
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Dihydrogen reduction of organic substrates using orthometallated ruthenium (II) complex catalysts
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New catalytic system of N,N′-diphenylurea synthesis from nitrobenzene, carbon monoxide and water or aniline
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SOME ASPECTS OF NITROALKANE HYDROGENATION VIA HOMOGENEOUS CATALYSIS
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Carbonylation and Hydroformylation
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Hydrogenation and related reactions
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SYNTHESIS AND PROPERTIES OF TRANSITION METAL TO CARBON BONDS
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References
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Environmentally safe magnetic/chitosan-based nickel schiff base composite as a heterogeneous and magnetically recoverable nanocatalyst for mild and efficient reduction of nitroarenes
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