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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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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.198206871openalex-snapshot
Mechanistic Aspects of the Carbonylation of Nitrobenzene with Rhodium Catalysts
inferredcites →https://doi.org/10.1002/anie.198904651openalex-snapshot
A Highly Selective Montmorillonite Catalyst for Hydrogenation of Alkynes, Alkenynes, and Alkadienes**
inferredcites →https://doi.org/10.1002/anie.199315241openalex-snapshot
Water‐Soluble Ligands, Metal Complexes, and Catalysts: Synergism of Homogeneous and Heterogeneous Catalysis
inferredcites →https://doi.org/10.1002/anie.199515241openalex-snapshot
Book Review: Derivative Spectrophotometry. Low and Higher Order. By G. Talsky
inferredcites →https://doi.org/10.1002/jlac.19535820102openalex-snapshot
Carbonylierung I. Über die Umsetzung von Acetylen mit Kohlenoxyd und Verbindungen mit reaktionsfähigen Wasserstoffatomen Synthesen α,β‐ungesättigter Carbonsäuren und ihrer Derivate
inferredcites →https://doi.org/10.1002/prac.19793210111openalex-snapshot
Zur Rhodium‐katalysierten Carbonylierung aromatischer Nitroverbindungen zu Isocyanaten. I. Katalysatoren und Reaktionsbedingungen
inferredcites →https://doi.org/10.1002/prac.19793210607openalex-snapshot
Zur Rhodium‐katalysierten Carbonylierung aromatischer Nitroverbindungen zu Isocyanaten. II. Untersuchungen zum Reaktionsmechanismus
inferredcites →https://doi.org/10.1002/zfch.19770171008openalex-snapshot
Die Carbonylierung aromatischer Nitroverbindungen zu Isocyanaten in Gegenart von Palladiumverbindungen; Die Carbonylierung von 2,4‐Dinitrotoluol zu Toluylen‐2,4‐diisocyanat in Gegenwart von PdCl2/(py)2/Fe2O3/FeVO4
inferredcites →https://doi.org/10.1002/zfch.19780180314openalex-snapshot
Die Carbonylierung aromatischer Nitroverbindungen zu Isocyanaten in Gegenwart von Palladiumverbindungen; Untersuchungen an den Fe2O3 · V2O5‐Kokatalysatoren
inferredcites →https://doi.org/10.1002/zfch.19800200807openalex-snapshot
Die Carbonylierung aromatischer Nitroverbindungen zu Isocyanaten in Gegenwart von Palladiumverbindungen; Die selektive Carbonylierung von 2‐Nitro‐1,3‐dialkylbenzenen unter Normaldruck
inferredcites →https://doi.org/10.1007/978-94-009-3897-7openalex-snapshot
Industrial Applications of Homogeneous Catalysis
inferredcites →https://doi.org/10.1007/978-94-011-3408-8openalex-snapshot
Metal Promoted Selectivity in Organic Synthesis
inferredcites →https://doi.org/10.1007/bf00771757openalex-snapshot
A highly active palladium complex catalyst in the synthesis of N,N?-diphenylurea from nitrobenzene, aniline and carbon monoxide
inferredcites →https://doi.org/10.1007/bf02705060openalex-snapshot
Selective conversion of nitrobenzene to phenylcarbamates catalyzed by Pd(II) and heteropolyacids
inferredcites →https://doi.org/10.1016/0022-328x(85)80207-2openalex-snapshot
Catalytic reductive carbonylation of aromatic nitro compounds to urethanes promoted by supported palladium activated with 1,10-phenanthroline derivatives
inferredcites →https://doi.org/10.1016/0022-328x(85)87437-4openalex-snapshot
Platinum complex catalyzed synthesis of urea derivatives from nitroarenes and amines under carbon monoxide
inferredcites →https://doi.org/10.1016/0022-328x(87)87174-7openalex-snapshot
Palladium-catalysed N,N′-disubstituted urea synthesis by oxidative carbonylation of amines under CO and O2 at atmospheric pressure
inferredcites →https://doi.org/10.1016/0022-328x(91)80175-jopenalex-snapshot
Catalysis by palladium salts
inferredcites →https://doi.org/10.1016/0022-328x(91)86451-uopenalex-snapshot
The role of alcohol in the catalytic reductive carbonylation of nitrobenzenes to carbamates in the presence of Rh(CO)4− or Ru3(CO)12
inferredcites →https://doi.org/10.1016/0022-328x(92)83101-mopenalex-snapshot
[Rh(CO)4]−, [Rh5(CO)15]−, and bimetallic clusters as catalysts for the carbonylation of nitrobenzene to methyl phenylcarbamate
inferredcites →https://doi.org/10.1016/0022-328x(93)83021-mopenalex-snapshot
Metal catalyzed deoxygenation by carbon monoxide of o-substituted nitrobenzenes. Synthesis of 1,4-dihydro-2H-3,1-benzoxazin- 2-one derivatives
inferredcites →https://doi.org/10.1016/0022-328x(94)05120-zopenalex-snapshot
New chelating nitrogen ligands and their application to the catalytic reduction of nitrobenzene to aniline. X-ray structure of [Rh(CO)2(BBOM)] (HBBOM = bis(2-benzoxazolyl)methane)
inferredcites →https://doi.org/10.1016/0040-4039(95)02003-8openalex-snapshot
First selective reduction of aromatic nitro compounds using water soluble catalysts
inferredcites →https://doi.org/10.1016/0166-9834(91)80103-4openalex-snapshot
New catalytic technology commercialized in the USA during the 1980's
inferredcites →https://doi.org/10.1016/0304-5102(81)85043-2openalex-snapshot
Facile reduction of nitrobenzene using carbon monoxide and water catalyzed by rhodium carbonyl cluster-amine systems
inferredcites →https://doi.org/10.1016/0304-5102(82)85041-4openalex-snapshot
Homogeneous catalytic reactions of methanol with carbon monoxide
inferredcites →https://doi.org/10.1016/0304-5102(83)80076-5openalex-snapshot
Catalytic reduction of nitroaromatic compounds with carbon monoxide and water using 3,4,7,8-Me4phen-carbonyl cluster systems as catalyst precursors: the role of chelating effect
inferredcites →https://doi.org/10.1016/0304-5102(84)85107-xopenalex-snapshot
Catalytic synthesis of aromatic urethanes from nitroaromatic compounds and carbon monoxide, using palladium + 1,10-phenanthroline derivatives as catalyst precursors
inferredcites →https://doi.org/10.1016/0304-5102(84)85131-7openalex-snapshot
Carbonylation of 2,4-dinitrotoluene using homogeneous Pd and Rh complex catalysts
inferredcites →https://doi.org/10.1016/0304-5102(85)85022-7openalex-snapshot
Applications of the water-gas shift reaction. use of the CO/H2O couple for the conversion of variolls organic substrates catalyzed by transition metal complexes
inferredcites →https://doi.org/10.1016/0304-5102(86)87071-7openalex-snapshot
Carbonylation of aromatic nitro compounds to isocyanates using a homogeneous trans-Pd(Py)2Cl2 complex catalyst: IR spectroscopic study and reaction mechanism
inferredcites →https://doi.org/10.1016/0304-5102(87)85040-xopenalex-snapshot
Reductive carbonylation of nitroaromatic compounds to urethanes catalyzed by [Pd(1,10-phenanthroline)2][PF6]2 and related complexes
inferredcites →https://doi.org/10.1016/0304-5102(88)80002-6openalex-snapshot
Cobalt-catalyzed reduction of aromatic nitro compounds
inferredcites →https://doi.org/10.1016/0304-5102(88)80021-xopenalex-snapshot
Homogeneous catalysis of the water-gas shift reaction
inferredcites →https://doi.org/10.1016/0304-5102(88)80055-5openalex-snapshot
Effects of neutral ligands in the reductive carbonylation of nitrobenzene catalysed by Ru3(CO)12 and Rh6(CO)16
inferredcites →https://doi.org/10.1016/0304-5102(89)80030-6openalex-snapshot
Reduction of nitrobenzene by dodecacarbonyl tri-iron under triphase conditions
inferredcites →https://doi.org/10.1016/0304-5102(90)85004-2openalex-snapshot
Reductive carbonylation of nitrobenzene to phenylurethane catalyzed by Ru(III)-schiff base complexes
inferredcites →https://doi.org/10.1016/0304-5102(90)85005-3openalex-snapshot
Kinetics and mechanism of the reductive carbonylation of nitrobenzene catalyzed by dichlorobis(salicylaldehyde)-o-phenylenediiminatoruthenate(III)
inferredcites →https://doi.org/10.1016/0304-5102(90)85121-wopenalex-snapshot
Useful synthesis of benzotriazole photostabilizers by reductive carbonylation of ortho-nitrophenylazo compounds, catalyzed by Ru3(CO)12 in the presence of NEt3
inferredcites →https://doi.org/10.1016/0304-5102(90)85150-gopenalex-snapshot
A highly selective palladium-catalyzed synthesis of N,N'-diphenylurea from nitrobenzene, aniline and carbon monoxide
inferredcites →https://doi.org/10.1016/0304-5102(91)80009-ropenalex-snapshot
Polar effects in the ruthenium(0)-catalysed reductive carbonylation of aromatic nitro derivatives to give ureas and amines
inferredcites →https://doi.org/10.1016/0304-5102(91)80159-zopenalex-snapshot
Synthesis of carbazole by Ru3(CO)12-catalyzed reductive carbonylation of 2-nitrobiphenyl: the crystal and molecular structure of Ru3(μ3-NC6H4-o-C6H5)2(CO)9
inferredcites →https://doi.org/10.1016/0304-5102(91)85013-ropenalex-snapshot
Facile selective reduction of aromatic nitro compounds affording amines using Rh4(CO)12-9,10-diaminophenanthrene catalyst system under CO/H2O conditions: The effect of 9,10-diaminophenanthrene
inferredcites →https://doi.org/10.1016/0304-5102(91)85055-7openalex-snapshot
Selective catalytic reduction of aromatic nitro compounds using CO and water with highly active rhodium-phosphine chelate complexes
inferredcites →https://doi.org/10.1016/0304-5102(91)85110-nopenalex-snapshot
Carbonylation of nitrobenzene to phenyl isocyanate and methyl carbamate catalyzed by palladium and rhodium activated by chelating nitrogen donor ligands
inferredcites →https://doi.org/10.1016/0304-5102(92)80028-fopenalex-snapshot
Reductive carbonylation of nitrobenzene catalyzed by heteropolyanion-modified palladium
inferredcites →https://doi.org/10.1016/0304-5102(92)80039-jopenalex-snapshot
Ruthenium(III)—Schiff base complex-catalyzed carbonylation of nitrobenzene to give phenylurethane
inferredcites →https://doi.org/10.1016/0304-5102(92)80054-kopenalex-snapshot
Novel selective catalytic reduction of aromatic nitro compounds affording amines using rutheniumcarbonyl complex in the presence of NEt3 under CO/H2O conditions
inferredcites →https://doi.org/10.1016/0304-5102(92)80060-topenalex-snapshot
Stoichiometry of palladium-catalyzed N, N′-diphenylurea synthesis from nitrobenzene, aniline and carbon monoxide
inferredcites →https://doi.org/10.1016/0304-5102(92)85006-2openalex-snapshot
Ruthenium carbonyl-catalyzed deoxygenation by carbon monoidde of o-substituted nitrobenzenes. Synthesis of benzimidazoles
inferredcites →https://doi.org/10.1016/0304-5102(93)85010-qopenalex-snapshot
Regiochemical synthesis of straight chain acids by the palladium (II) catalysed hydrocarboxylation of olefins with oxalic acid
inferredcites →https://doi.org/10.1016/0304-5102(93)87057-fopenalex-snapshot
Selective reduction of aromatic nitro compounds affording aromatic amines under CO/H2O conditions catalyzed by phosphine-added rhodium and ruthenium carbonyl complexes
inferredcites →https://doi.org/10.1016/0304-5102(93)87117-qopenalex-snapshot
Reduction of nitrobenzene to aniline by CO/H2O, catalysed by Ru3 (CO)12. Strong activating ability of rigid α-diimine ligands
inferredcites →https://doi.org/10.1016/0304-5102(93)e0228-9openalex-snapshot
Synthesis of heterocycles via palladium-catalyzed carbonylation of ortho-substituted organic nitro compounds in relatively mild conditions
inferredcites →https://doi.org/10.1016/0304-5102(93)e0250-kopenalex-snapshot
An efficient heterogenised palladium catalytic system for the reductive carbonylation of nitrobenzene to methyl N-phenylcarbamate
inferredcites →https://doi.org/10.1016/0304-5102(93)e0324-aopenalex-snapshot
Palladium-catalyzed hydroesterification of alkynes in the presence of p-toluenesulfonic acid under a normal pressure of carbon monoxide
inferredcites →https://doi.org/10.1016/0304-5102(93)e0347-jopenalex-snapshot
Chemoselective reduction of nitro groups in the presence of olefinic, ester, and halogeno functions using a reducing agent of CO and H2O catalyzed by Rh carbonyl clusters
inferredcites →https://doi.org/10.1016/0304-5102(93)e3136-oopenalex-snapshot
Triruthenium dodecacarbonyl-catalyzed reductive carbonylation of nitroarenes: cyclization, carbon monoxide insertion and reduction. An overview
inferredcites →https://doi.org/10.1016/0304-5102(94)00024-7openalex-snapshot
Orthometalated ruthenium-complex-catalysed reductive carbonylation of nitroaromatics
inferredcites →https://doi.org/10.1016/0304-5102(94)00035-2openalex-snapshot
Activity and selectivity of supported Rh complex catalyst in carbonylation of nitrobenzene
inferredcites →https://doi.org/10.1016/1381-1169(94)00133-2openalex-snapshot
Efficient selective reduction of aromatic nitro compounds by ruthenium catalysis under COH2O conditions
inferredcites →https://doi.org/10.1016/b978-0-12-605355-5.50009-4openalex-snapshot
Hydrogenation of Ketones
inferredcites →https://doi.org/10.1016/s0040-4039(00)74325-5openalex-snapshot
Direct, regioselective hydrocarboxylation of alkynes to saturated acids by cobalt and nickel catalysts under phase transfer conditions
inferredcites →https://doi.org/10.1016/s0040-4039(00)90615-4openalex-snapshot
The direct conversion of aromatic nitro compounds to isocyanates by carbon monoxide
inferredcites →https://doi.org/10.1016/s0040-4039(00)92816-8openalex-snapshot
The ruthenium carbonyl catalyzed reduction of nitro compounds by phase transfer catalysis
inferredcites →https://doi.org/10.1016/s0277-5387(00)86350-0openalex-snapshot
Halide promotion of the formation and carbonylation of μ3-imido ligands. Relevance to the halide promotion of nitroaromatic carbonylation catalysis
inferredcites →https://doi.org/10.1021/cr00028a008openalex-snapshot
Transformations of Chloroarenes, Catalyzed by Transition-Metal Complexes
inferredcites →https://doi.org/10.1021/i200027a028openalex-snapshot
Carbonylation of nitrobenzene to phenyl isocyanate using palladium complex catalysts. Screening of catalysts and kinetic study
inferredcites →https://doi.org/10.1021/ic00019a011openalex-snapshot
Homogeneous catalytic carbonylation of nitroaromatics. 4. Preparation and characterization of ruthenium radical cations
inferredcites →https://doi.org/10.1021/ic00080a012openalex-snapshot
Homogeneous catalytic carbonylation of nitroaromatics. 6. Synthesis and structure of two bis(carbamoyl) complexes of ruthenium
inferredcites →https://doi.org/10.1021/ie00055a009openalex-snapshot
Palladium-catalyzed synthesis of N,N'-diphenylurea from nitrobenzene, aniline, and carbon monoxide
inferredcites →https://doi.org/10.1021/ja00003a056openalex-snapshot
Homogeneous catalytic carbonylation of nitroaromatics. 2. Characterization of two intermediates, Ru[C(O)N(Ar)O][Ph2P(CH2)2PPh2](CO)2 and Ru[C(O)OCH3]2[Ph2P(CH2)2PPh2](CO)2, and evidence for the carbamate-forming step
inferredcites →https://doi.org/10.1021/ja00040a082openalex-snapshot
Palladium(II) catalysts for living alternating copolymerization of olefins and carbon monoxide
inferredcites →https://doi.org/10.1021/ja00049a026openalex-snapshot
Homogeneous catalytic carbonylation of nitroaromatics. 5. Kinetics and mechanism of aniline and carbamate formation using ruthenium complex Ru(Ph2PCH2CH2PPh2)(CO)3
inferredcites →https://doi.org/10.1021/ja00062a055openalex-snapshot
Reductive carbonylation of mono- and dinitroarenes catalyzed by montmorillonitebipyridinylpalladium(II) acetate and ruthenium carbonyl
inferredcites →https://doi.org/10.1021/ja00088a015openalex-snapshot
Homogeneous Catalytic Carbonylation of Nitroaromatics. 8. Kinetic and Mechanistic Studies of the Carbon-Nitrogen Bond and Product Forming Steps from Ru(Ph2PCH2CH2PPh2)(CO)2[C(O)OCH3]2: The Turnover Limiting Reactions in the Catalytic Cycle
inferredcites →https://doi.org/10.1021/ja00120a012openalex-snapshot
Indirect Formation of Carboxylic Acids via Anhydrides in the Palladium-Catalyzed Hydroxycarbonylation of Aromatic Halides
inferredcites →https://doi.org/10.1021/ja00175a050openalex-snapshot
The remarkable cobalt- and phase-transfer-catalyzed carbonylation of epoxy alcohols: a formal triple carbonylation reaction
inferredcites →https://doi.org/10.1021/ja00411a050openalex-snapshot
Iron and ruthenium carbonyl catalyzed reductive carbonylation of nitro compounds by sodium methoxide. A significant effect of the metal on the reaction course
inferredcites →https://doi.org/10.1021/ja00480a075openalex-snapshot
Catalytic reductions using carbon monoxide and water in place of hydrogen. 2. Reduction of aromatic nitro compounds to amines
inferredcites →https://doi.org/10.1021/ja00539a055openalex-snapshot
Intramolecular proton exchange in aqueous histamine. An NMR method for resolving the ammonium and imidazole proton-exchange rates
inferredcites →https://doi.org/10.1021/ja00752a099openalex-snapshot
New synthesis of ureas. Reaction of ammonia or aliphatic amines with carbon monoxide in the presence of selenium
inferredcites →https://doi.org/10.1021/jo00003a036openalex-snapshot
Palladium(II)-catalyzed carbonylation of 3-buten-1-ols and 3-butyn-1-ols: an efficient synthesis of .gamma.-butyrolactones
inferredcites →https://doi.org/10.1021/jo00054a008openalex-snapshot
Transition-metal complex-catalyzed reductive N-heterocyclization: synthesis of 4(3H)-quinazolinone derivatives from N-(2-nitrobenzoyl)amides
inferredcites →https://doi.org/10.1021/jo00091a026openalex-snapshot
Palladium Complex-Catalyzed Reductive N-Heterocyclization of Nitroarenes: Novel Synthesis of Indole and 2H-Indazole Derivatives
inferredcites →https://doi.org/10.1021/jo00106a042openalex-snapshot
Hydroesterification of Olefins Catalyzed by Pd(OAc)2 Immobilized on Montmorillonite
inferredcites →https://doi.org/10.1021/jo00241a023openalex-snapshot
Ruthenium carbonyl catalyzed reductive carbonylation of aromatic nitro compounds. A selective route to carbamates
inferredcites →https://doi.org/10.1021/jo00907a025openalex-snapshot
Low-pressure, palladium-catalyzed N,N'-diarylurea synthesis from nitro compounds, amines, and carbon monoxide
inferredcites →https://doi.org/10.1021/jo00947a014openalex-snapshot
Synthesis of aryl isocyanates from nitro compounds and carbon monoxide
inferredcites →https://doi.org/10.1021/jo00982a049openalex-snapshot
Catalytic deoxygenation of organic compounds by carbon monoxide. II. Direct synthesis of Schiff bases from aromatic nitro derivatives, aldehydes, and carbon monoxide
inferredcites →https://doi.org/10.1021/jo01020a002openalex-snapshot
Diborane Reduction of Nitro Salts. A New Synthesis of N-Monosubstituted Hydroxylamines
inferredcites →https://doi.org/10.1021/jo01067a067openalex-snapshot
A New Synthesis of Ureas. III. The Reaction of Aromatic Amines with Carbon Monoxide and Sulfur
inferredcites →https://doi.org/10.1021/om00008a024openalex-snapshot
Subtle Balance between Various Phenanthroline Ligands and Anions in the Palladium-Catalyzed Reductive Carbonylation of Nitrobenzene
inferredcites →https://doi.org/10.1021/om00016a022openalex-snapshot
Mechanistic Study of the Carbonylation of Nitrobenzene Catalyzed by the [Rh(CO)4]-/Nitrogen Base System. X-ray Structure of [cyclic] [PPN][Rh(CO)2ON(C6H3Cl2)C(O)O]
inferredcites →https://doi.org/10.1021/om00023a005openalex-snapshot
Homogeneous Catalytic Carbonylation of Nitroaromatics. 9. Kinetics and Mechanism of the First N-O Bond Cleavage and Structure of the .eta.2-ArNO Intermediate
inferredcites →https://doi.org/10.1021/om00024a031openalex-snapshot
Ligand Effects in the Palladium-Catalyzed Reductive Carbonylation of Nitrobenzene
inferredcites →https://doi.org/10.1021/om00029a049openalex-snapshot
Nickel- and phase-transfer-catalyzed carboxylation of propargyl and allenyl halides
inferredcites →https://doi.org/10.1021/om00049a049openalex-snapshot
Stereoselective synthesis of diacids by the nickel cyanide and phase-transfer-catalyzed carbonylation of alkynols. Novel dependency of product stereochemistry and optimum stirring speed on the nature of the phase-transfer agent
inferredcites →https://doi.org/10.1021/om00054a070openalex-snapshot
Palladium chloride catalyzed dicarbonylation of terminal alkynes
inferredcites →https://doi.org/10.1021/om00069a024openalex-snapshot
Selective carbonylation of nitrobenzene over a mixed palladium-molybdenum cluster-derived catalyst
inferredcites →https://doi.org/10.1021/om00111a006openalex-snapshot
Further studies of cluster-bound imido ligands. Imido-acyl coupling and promotion of the formation and carbonylation of imido ligands by halides
inferredcites →https://doi.org/10.1039/c39820000935openalex-snapshot
A Rh cluster which selectively reduces aldehyde functions using co and H2O as the hydrogen source
inferredcites →https://doi.org/10.1039/c39840001286openalex-snapshot
Selective ruthenium carbonyl catalysed reductive carbonylation of aromatic nitro compounds to carbamates
inferredcites →https://doi.org/10.1039/c39860000784openalex-snapshot
Deoxygenation reactions of ortho-nitrostyrenes with carbon monoxide catalysed by metal carbonyls: a new route to indoles
inferredcites →https://doi.org/10.1039/c39900001616openalex-snapshot
The palladium catalysed carbonylation of nitrobenzene into phenyl isocyanate: a metallacyclic intermediate
inferredcites →https://doi.org/10.1039/c39920001467openalex-snapshot
Mechanistic studies of the carbonylation of nitrobenzene catalysed by the [Rh(CO) 4 ] – /bipy system. X-Ray structure of [PPN][Rh(CO) 2 ON[C 6 H 3 Cl 2 )C(O)O]; [PPN + =(PPh 3 ) 2 N + ; bipy = 2,2′-bipyridyl]
inferredcites →https://doi.org/10.1039/c39940001741openalex-snapshot
Intramolecular amination of olefins. Synthesis of 2-substituted-4-quinolones from 2-nitrochalcones catalysed by ruthenium
inferredcites →https://doi.org/10.1039/ft9918702811openalex-snapshot
Chemometric optimization of the ruthenium carbonyl catalysed cyclization of 2-nitrostilbene to 2-phenylindole
inferredcites →https://doi.org/10.1039/p29940000913openalex-snapshot
Role of alkali halides in the synthesis of nitrogen containing heterocycles by reductive carbonylation of aromatic nitro-derivatives catalysed by Ru3(CO)12
inferredcites →https://doi.org/10.1070/rc1981v050n05abeh002628openalex-snapshot
Synthesis of Nitrogen-containing Compounds by the Interaction of Nitro-compounds with Carbon Monoxide
inferredcites →https://doi.org/10.1246/bcsj.56.3343openalex-snapshot
The Platinum Complex Catalyzed Reductive N-Carbonylation of Nitroarenes to the Carbamates
inferredcites →https://doi.org/10.1246/bcsj.57.2867openalex-snapshot
The Platinum Catalyzed Reduction of Nitroarenes to Aminoarenes with Carbon Monoxide and Water
inferredcites →https://doi.org/10.1246/bcsj.57.3011openalex-snapshot
The Platinum Complex-catalyzed Reductive N-Carbonylation of Dinitroarenes to the Biscarbamates
inferredcites →https://doi.org/10.1246/bcsj.63.640openalex-snapshot
A Facile, Practical Synthesis of 2-(6-Methoxy-2-naphthyl)propenoic Acid
inferredcites →https://doi.org/10.1246/bcsj.64.2624openalex-snapshot
Efficient Selective Reduction of Aromatic Nitro Compounds Affording Aromatic Amines under CO/H2O Conditions Catalyzed by Amine-Added Rhodium–Carbonyl Complexes
inferredcites →https://doi.org/10.1246/bcsj.67.2329openalex-snapshot
Formylation of Aryl Halides with Carbon Monoxide and Sodium Formate in the Presence of Palladium Catalyst
inferredcites →https://doi.org/10.1246/cl.1982.105openalex-snapshot
THE PLATINUM COMPLEX CATALYZED REDUCTIVE CARBONYLATION OF NITROARENE TO URETHANE
inferredcites →https://doi.org/10.1246/cl.1990.795openalex-snapshot
Heteropoly Anion-Modifled Palladium Catalyst for Reductive Carbonylation of Nitrobenzene
inferredcites →https://doi.org/10.1246/cl.1991.1673openalex-snapshot
Organic Iodide Aided Carbonylation of Terminal Acetylenes with Palladium Catalyst
inferredcites →https://doi.org/10.1246/cl.1991.1679openalex-snapshot
Selective Catalytic Reduction of Aromatic Nitro Compounds Affording Amines under CO/H2O Conditions Using Amine-added Ruthenium–Carbonyl Complexes
inferredcites →https://doi.org/10.1351/pac199062040661openalex-snapshot
Opportunities in homogeneous catalysis
inferredcites →https://doi.org/10.1351/pac199163050687openalex-snapshot
Mechanisms of double and single carbonylation reactions catalyzed by palladium complexes
inferredcites →https://doi.org/10.1627/jpi1958.34.160openalex-snapshot
Carbonylation of nitrobenzene 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.3919708openalex-extracted
Copper on Carbamate-Isocyanurate-Bridged Periodic Mesoporous Organosilica: An Efficient Catalyst for Sustainable and Selective Alcohol Oxidation
inferred← citeshttps://doi.org/10.2139/ssrn.4639751openalex-extracted
[Ns]-Chelate Half-Sandwich Iridium Complexes: Synthesis, Structure and Catalytic Hydrogenation Activity
inferred← citeshttps://doi.org/10.2139/ssrn.4657274openalex-extracted
[Ns]-Chelate Half-Sandwich Iridium Complexes: Synthesis, Structure and Catalytic Hydrogenation Activity
inferred← citeshttps://doi.org/10.1002/(sici)1099-0739(199807)12:7<520::aid-aoc747>3.0.co;2-topenalex-snapshot
Book Review: Chemistry of Tin, 2nd edition, P.J. Smith (ed). Blackie Academic & Professional, London, 1997. 578 pages. �149 (hardback). ISBN 0-7514-0385-7
inferred← citeshttps://doi.org/10.1002/(sici)1099-0739(199807)12:7<520::aid-aoc748>3.0.co;2-qopenalex-snapshot
Book Review: Catlytic Reductive Carbonylation of Organic Nitro Compunds. S. Cenini and F. Ragaini. Kluwer Academic Publishers, Dordect, 1996. 339 + xi pages. �115. ISBN 0-7923-4307-7
inferred← citeshttps://doi.org/10.1002/047084289x.rn00417openalex-snapshot
Copper(II) Toluenesulfonate
inferred← citeshttps://doi.org/10.1002/1099-0682(200011)2000:11<2351::aid-ejic2351>3.0.co;2-#openalex-snapshot
Synthesis and Crystal Structure of a Palladium Metallacyclic Complex: A Key Intermediate in the Carbonylation of Azobenzene to N ‐Phenyl Urethane
inferred← citeshttps://doi.org/10.1002/9781118662083.cot05-007openalex-snapshot
Formation of Amines from Nitro Compounds
inferred← citeshttps://doi.org/10.1002/9781118901274.ch2openalex-snapshot
Polyurethane Building Blocks
inferred← citeshttps://doi.org/10.1002/9781119669401.ch2openalex-snapshot
POLYURETHANE BUILDING BLOCKS
inferred← citeshttps://doi.org/10.1002/9781119783435.ch18openalex-snapshot
Fluorescent Probes for Intracellular Carbon Monoxide Detection
inferred← citeshttps://doi.org/10.1002/9783527618231.ch3aopenalex-snapshot
Development of Methods: Section 3.1.1–3.1.2.2.4
inferred← citeshttps://doi.org/10.1002/9783527651733.ch21openalex-snapshot
Carbonylation of Nitroarenes and Aromatic Amines
inferred← citeshttps://doi.org/10.1002/9783527830190.ch14openalex-snapshot
Natural Phosphates and Their Catalytic Applications
inferred← citeshttps://doi.org/10.1002/9783527831883.ch16openalex-snapshot
Carbonylation of Nitroarenes and Related Compounds
inferred← citeshttps://doi.org/10.1002/adsc.200303143openalex-snapshot
Phosphorus Acids as Highly Efficient Promoters for the Palladium‐Phenanthroline Catalyzed Carbonylation of Nitrobenzene to Methyl Phenylcarbamate†
inferred← citeshttps://doi.org/10.1002/adsc.200303244openalex-snapshot
Selenium‐Catalyzed Carbonylation of Nitroarenes to Symmetrical 1,3‐Diarylureas under Atmospheric Pressure
inferred← citeshttps://doi.org/10.1002/adsc.200404077openalex-snapshot
N‐Arylamides from Selenium‐Catalyzed Reactions of Nitroaromatics and Amides in the Presence of Carbon Monoxide and Mixed Organic Bases
inferred← citeshttps://doi.org/10.1002/adsc.200404151openalex-snapshot
Carbonylation of Dinitrotoluene to Dimethyl Toluenedicarbamate; High Efficiency of Phosphorus Acids as Promoters for the Palladium‐Phenanthroline Catalytic System
inferred← citeshttps://doi.org/10.1002/adsc.200700070openalex-snapshot
Efficient Reduction of Nitroarenes over Nickel‐Iron Mixed Oxide Catalyst Prepared from a Nickel‐Iron Hydrotalcite Precursor
inferred← citeshttps://doi.org/10.1002/adsc.201000191openalex-snapshot
Highly Chemo‐ and Regioselective Reduction of Aromatic Nitro Compounds Catalyzed by Recyclable Copper(II) as well as Cobalt(II) Phthalocyanines
inferred← citeshttps://doi.org/10.1002/adsc.201100545openalex-snapshot
Palladium‐Catalyzed Carbonylation of Amines: Switchable Approaches to Carbamates and N,N′‐Disubstituted Ureas
inferred← citeshttps://doi.org/10.1002/adsc.201200356openalex-snapshot
Ruthenium Nanoparticle‐Catalyzed, Controlled and Chemoselective Hydrogenation of Nitroarenes using Ethanol as a Hydrogen Source
inferred← citeshttps://doi.org/10.1002/adsc.201300745openalex-snapshot
Cobalt(II)‐Catalyzed Isocyanide Insertion Reaction with Amines under Ultrasonic Conditions: A Divergent Synthesis of Ureas, Thioureas and Azaheterocycles
inferred← citeshttps://doi.org/10.1002/adsc.201501131openalex-snapshot
An Efficient, Stable and Reusable Palladium Nanocatalyst: Chemoselective Reduction of Aldehydes with Molecular Hydrogen in Water
inferred← citeshttps://doi.org/10.1002/adsc.201700944openalex-snapshot
Supported Palladium Nanoparticles Catalyzed Reductive Carbonylation of Nitroarenes to N‐Arylformamides
inferred← citeshttps://doi.org/10.1002/adsc.201800495openalex-snapshot
Oxidative Coupling of Aromatic Amines and Nitrosoarenes: Iodine‐Mediated Formation of Unsymmetrical Aromatic Azoxy Compounds
inferred← citeshttps://doi.org/10.1002/adsc.201800496openalex-snapshot
A Palladium‐Catalyzed Domino Procedure for the Synthesis of Unsymmetrical Ureas
inferred← citeshttps://doi.org/10.1002/adsc.201800954openalex-snapshot
Pd/C‐Catalyzed Domino Synthesis of Urea Derivatives Using Chloroform as the Carbon Monoxide Source in Water
inferred← citeshttps://doi.org/10.1002/adsc.201801175openalex-snapshot
Synthesis of Unsymmetrical Aromatic Azoxy Compounds by Silver‐Mediated Oxidative Coupling of Aromatic Amines with Nitrosoarenes
inferred← citeshttps://doi.org/10.1002/adsc.201900185openalex-snapshot
Metal‐free Carbon Monoxide (CO) Capture and Utilization: Formylation of Amines
inferred← citeshttps://doi.org/10.1002/adsc.202000370openalex-snapshot
Recent Progress on Reductive Coupling of Nitroarenes by Using Organosilanes as Convenient Reductants
inferred← citeshttps://doi.org/10.1002/adsc.202001245openalex-snapshot
Liquid‐Assisted Grinding Mechanochemistry in the Synthesis of Pharmaceuticals
inferred← citeshttps://doi.org/10.1002/adsc.202100236openalex-snapshot
A Metal‐Free Direct Arene C−H Amination
inferred← citeshttps://doi.org/10.1002/adsc.202101490openalex-snapshot
“Urea to Urea” Approach: Access to Unsymmetrical Ureas Bearing Pyridyl Substituents
inferred← citeshttps://doi.org/10.1002/adsc.202401034openalex-snapshot
Iron‐Catalyzed Reductive Coupling of Nitro Compounds with Grignard and Organozinc Reagents for Synthesis of Functionalized Secondary Amines
inferred← citeshttps://doi.org/10.1002/ajoc.201300016openalex-snapshot
Synthesis of Pyrroles, Indoles, and Carbazoles through Transition‐Metal‐Catalyzed CH Functionalization
inferred← citeshttps://doi.org/10.1002/ajoc.201402249openalex-snapshot
Catalyst‐Free Chemoselective Reduction of Nitroarenes Using Thiourea as a Hydrogen Source
inferred← citeshttps://doi.org/10.1002/ajoc.201402251openalex-snapshot
Direct ortho ‐Acylation of Azoxybenzenes with Aldehydes via Palladium‐Catalyzed Regioselective CH Bond Activation
inferred← citeshttps://doi.org/10.1002/ajoc.202100440openalex-snapshot
Highly Selective Monoalkylation of Active Methylene and Related Derivatives using Alkylsilyl Peroxides by a Catalytic CuI‐DMAP System
inferred← citeshttps://doi.org/10.1002/ajoc.202100495openalex-snapshot
Recent Advances in Hydrogenation Reactions Using Bimetallic Nanocatalysts: A Review
inferred← citeshttps://doi.org/10.1002/ajoc.202400255openalex-snapshot
Reductive C−N Bond Formation of Nitroarenes Using Pd@rGO‐CuFe2O4 Magnetic Nanoparticles in Water towards the Synthesis of N‐Aryl Formamide and Azole Derivatives
inferred← citeshttps://doi.org/10.1002/ange.200351004openalex-snapshot
The Carbonylation Reaction of Nitrobenzene to Methyl Phenylcarbamate: Highly Efficient Promoters for the Palladium–Phenanthroline Catalytic System Based on Phosphorus Acids
inferred← citeshttps://doi.org/10.1002/ange.200351098openalex-snapshot
Alternatives to Phosgene and Carbon Monoxide: Synthesis of Symmetric Urea Derivatives with Carbon Dioxide in Ionic Liquids
inferred← citeshttps://doi.org/10.1002/ange.200904647openalex-snapshot
Efficient and Selective Room‐Temperature Gold‐Catalyzed Reduction of Nitro Compounds with CO and H2O as the Hydrogen Source
inferred← citeshttps://doi.org/10.1002/ange.201205792openalex-snapshot
In Situ Generated Iron Oxide Nanocrystals as Efficient and Selective Catalysts for the Reduction of Nitroarenes using a Continuous Flow Method
inferred← citeshttps://doi.org/10.1002/ange.201400059openalex-snapshot
Reduktive Aminierung ohne externe Wasserstoffquelle
inferred← citeshttps://doi.org/10.1002/ange.201410605openalex-snapshot
Base‐Promoted Coupling of Carbon Dioxide, Amines, and N‐Tosylhydrazones: A Novel and Versatile Approach to Carbamates
inferred← citeshttps://doi.org/10.1002/ange.201600906openalex-snapshot
Carbokatalyse in Flüssigphasenreaktionen
inferred← citeshttps://doi.org/10.1002/ange.201601803openalex-snapshot
Die Wassergas‐Shift‐Reaktion in der organischen Synthese
inferred← citeshttps://doi.org/10.1002/ange.201601989openalex-snapshot
Positioning a Carbon–Fluorine Bond over the π Cloud of an Aromatic Ring: A Different Type of Arene Activation
inferred← citeshttps://doi.org/10.1002/ange.201705356openalex-snapshot
Electrophilic Amination with Nitroarenes
inferred← citeshttps://doi.org/10.1002/ange.202204561openalex-snapshot
Near‐Infrared Light‐Driven Photoredox Catalysis by Transition‐Metal‐Complex Nanodots
inferred← citeshttps://doi.org/10.1002/ange.202207252openalex-snapshot
Microenvironment Engineering for the Electrocatalytic CO2 Reduction Reaction
inferred← citeshttps://doi.org/10.1002/anie.200351004openalex-snapshot
The Carbonylation Reaction of Nitrobenzene to Methyl Phenylcarbamate: Highly Efficient Promoters for the Palladium–Phenanthroline Catalytic System Based on Phosphorus Acids
inferred← citeshttps://doi.org/10.1002/anie.200351098openalex-snapshot
Alternatives to Phosgene and Carbon Monoxide: Synthesis of Symmetric Urea Derivatives with Carbon Dioxide in Ionic Liquids
inferred← citeshttps://doi.org/10.1002/anie.200904647openalex-snapshot
Efficient and Selective Room‐Temperature Gold‐Catalyzed Reduction of Nitro Compounds with CO and H2O as the Hydrogen Source
inferred← citeshttps://doi.org/10.1002/anie.201205792openalex-snapshot
In Situ Generated Iron Oxide Nanocrystals as Efficient and Selective Catalysts for the Reduction of Nitroarenes using a Continuous Flow Method
inferred← citeshttps://doi.org/10.1002/anie.201400059openalex-snapshot
Reductive Amination without an External Hydrogen Source
inferred← citeshttps://doi.org/10.1002/anie.201410605openalex-snapshot
Base‐Promoted Coupling of Carbon Dioxide, Amines, and N‐Tosylhydrazones: A Novel and Versatile Approach to Carbamates
inferred← citeshttps://doi.org/10.1002/anie.201600906openalex-snapshot
Carbocatalysis in Liquid‐Phase Reactions
inferred← citeshttps://doi.org/10.1002/anie.201601803openalex-snapshot
Harnessing the Power of the Water‐Gas Shift Reaction for Organic Synthesis
inferred← citeshttps://doi.org/10.1002/anie.201601989openalex-snapshot
Positioning a Carbon–Fluorine Bond over the π Cloud of an Aromatic Ring: A Different Type of Arene Activation
inferred← citeshttps://doi.org/10.1002/anie.201705356openalex-snapshot
Electrophilic Amination with Nitroarenes
inferred← citeshttps://doi.org/10.1002/anie.202204561openalex-snapshot
Near‐Infrared Light‐Driven Photoredox Catalysis by Transition‐Metal‐Complex Nanodots
inferred← citeshttps://doi.org/10.1002/anie.202207252openalex-snapshot
Microenvironment Engineering for the Electrocatalytic CO 2 Reduction Reaction
inferred← citeshttps://doi.org/10.1002/aoc.1292openalex-snapshot
Fluoride effect on the palladium–phenanthroline catalyzed carbonylation of nitroarenes to carbamates
inferred← citeshttps://doi.org/10.1002/aoc.1577openalex-snapshot
A study on the heterobinuclear site of Co(salen)/TiO2SiO2 catalysts in the oxidative carbonylation of aniline
inferred← citeshttps://doi.org/10.1002/aoc.3975openalex-snapshot
Chemo‐selective reduction of nitro and nitrile compounds using Ni nanoparticles immobilized on hyperbranched polymer‐functionalized magnetic nanoparticles
inferred← citeshttps://doi.org/10.1002/aoc.4132openalex-snapshot
Magnetically Recyclable Metal–Organic Framework@Fe3O4 Composite‐Catalyzed Facile Reduction of Nitroarene Compounds in Aqueous Medium
inferred← citeshttps://doi.org/10.1002/aoc.5223openalex-snapshot
Fe3O4 – Glutathione stabilized Ag nanoparticles: A new magnetically separable robust and facile catalyst for aqueous phase reduction of nitroarenes
inferred← citeshttps://doi.org/10.1002/aoc.5289openalex-snapshot
Half‐sandwich ruthenium complexes with S chiff base ligands bearing a hydroxyl group: Preparation, characterization and catalytic activities
inferred← citeshttps://doi.org/10.1002/aoc.5499openalex-snapshot
Synthesis of water soluble Pd‐Piperidoimidazolin‐2‐ylidene complexes and their catalytic activities in neat water
inferred← citeshttps://doi.org/10.1002/aoc.5626openalex-snapshot
Synthetic application of gold complexes on magnetic supports
inferred← citeshttps://doi.org/10.1002/aoc.5651openalex-snapshot
Synthesis, characterization, and catalytic activity of half‐sandwich ruthenium complexes with pyridine/phenylene bridged NHC = E (NHC = N‐heterocyclic carbene, E = S, Se) ligands
inferred← citeshttps://doi.org/10.1002/aoc.7107openalex-snapshot
Ru(II) and Ru(III) complexes containing N‐acylthiourea ligands: Supramolecular structures and synthons, reduction, and reaction pathway of aromatic nitro compounds
inferred← citeshttps://doi.org/10.1002/aoc.7287openalex-snapshot
Recent advances in β‐cyclodextrin‐based catalysts for reducing toxic nitroaromatic: An overview
inferred← citeshttps://doi.org/10.1002/asia.201100311openalex-snapshot
Fe 3 O 4 Nanoparticles: A Conveniently Reusable Catalyst for the Reduction of Nitroarenes Using Hydrazine Hydrate
inferred← citeshttps://doi.org/10.1002/asia.202100321openalex-snapshot
Rhodium‐terpyridine Catalyzed Transfer Hydrogenation of Aromatic Nitro Compounds in Water
inferred← citeshttps://doi.org/10.1002/asia.202400464openalex-snapshot
Polyoxometalates Based Catalysts for Carbonylation Reactions: A Review
inferred← citeshttps://doi.org/10.1002/asia.70897openalex-snapshot
Visible‐Light‐Driven Photoredox‐Catalyzed Reduction of Nitro (Hetero)arenes to (Hetero)aryl Amines and Subsequent C─N Bond‐Forming Reactions
inferred← citeshttps://doi.org/10.1002/bab.1189openalex-snapshot
Catalytic and synergistic antibacterial potential of green synthesized silver nanoparticles: Their ecotoxicological evaluation on Poecillia reticulata
inferred← citeshttps://doi.org/10.1002/bkcs.11363openalex-snapshot
One‐Pot Synthesis of Disubstituted Urea from Carbon Dioxide, Propylene Oxide, and Amines Catalyzed by Imidazolium‐Tetraiodoindate
inferred← citeshttps://doi.org/10.1002/cctc.201300769openalex-snapshot
Nanopalladium on Amino‐Functionalized Mesocellular Foam as an Efficient and Recyclable Catalyst for the Selective Transfer Hydrogenation of Nitroarenes to Anilines
inferred← citeshttps://doi.org/10.1002/cctc.201300821openalex-snapshot
Platinum N‐Heterocyclic Carbene Nanoparticles as New and Effective Catalysts for the Selective Hydrogenation of Nitroaromatics
inferred← citeshttps://doi.org/10.1002/cctc.201500493openalex-snapshot
Reductive Transformations of Carbonyl Compounds Catalyzed by Rhodium Supported on a Carbon Matrix by using Carbon Monoxide as a Deoxygenative Agent
inferred← citeshttps://doi.org/10.1002/cctc.201600296openalex-snapshot
Base‐Free Transfer Hydrogenation of Nitroarenes Catalyzed by Micro‐Mesoporous Iron Oxide
inferred← citeshttps://doi.org/10.1002/cctc.201700095openalex-snapshot
Metal–Organic Framework Mediated Cobalt/Nitrogen‐Doped Carbon Hybrids as Efficient and Chemoselective Catalysts for the Hydrogenation of Nitroarenes
inferred← citeshttps://doi.org/10.1002/cctc.201700880openalex-snapshot
Bimetallic Platinum‐Tin Nanoparticles on Hydrogenated Molybdenum Oxide for the Selective Hydrogenation of Functionalized Nitroarenes
inferred← citeshttps://doi.org/10.1002/cctc.201701214openalex-snapshot
Synthesis of N‐Heterocycles by Reductive Cyclization of Nitro Compounds using Formate Esters as Carbon Monoxide Surrogates
inferred← citeshttps://doi.org/10.1002/cctc.201801223openalex-snapshot
Synthesis of 3,6‐Dihydro‐2H‐[1, 2]‐Oxazines from Nitroarenes and Conjugated Dienes, Catalyzed by Palladium/Phenanthroline Complexes and Employing Phenyl Formate as a CO Surrogate
inferred← citeshttps://doi.org/10.1002/cctc.201801626openalex-snapshot
Fe/Fe2O3@N‐dopped Porous Carbon: A High‐Performance Catalyst for Selective Hydrogenation of Nitro Compounds
inferred← citeshttps://doi.org/10.1002/cctc.201901065openalex-snapshot
Transition Metal Catalyzed Reductive Cyclization Reactions of Nitroarenes and Nitroalkenes
inferred← citeshttps://doi.org/10.1002/cctc.201901491openalex-snapshot
Rh Catalyzed Selective Hydrogenation of Nitroarenes under Mild Conditions: Understanding the Functional Groups Attached to the Nanoparticles
inferred← citeshttps://doi.org/10.1002/cctc.202000274openalex-snapshot
Titania Morphology‐Dependent Catalysis of CuOx/TiO2 Catalysts in CO Oxidation and Water Gas Shift Reactions
inferred← citeshttps://doi.org/10.1002/cctc.202000683openalex-snapshot
In Situ Synthesized Silica‐Supported Co@N‐Doped Carbon as Highly Efficient and Reusable Catalysts for Selective Reduction of Halogenated Nitroaromatics
inferred← citeshttps://doi.org/10.1002/cctc.202100344openalex-snapshot
Cyclobutadiene Rhodium Complexes as Catalysts for the Synthesis of Amides from Electron‐rich Arenes, Tosyl Azide and CO
inferred← citeshttps://doi.org/10.1002/cctc.202401933openalex-snapshot
Pyridinium Amidate Ligands for Efficient Pd‐Catalyzed Reductive Nitroarene Cyclization Using Formate as CO Surrogate
inferred← citeshttps://doi.org/10.1002/cctc.202500383openalex-snapshot
Copper‐Catalyzed Hydrosilylation of Nitroarenes: Chemoselective Reduction to Aromatic Amines
inferred← citeshttps://doi.org/10.1002/ceat.201800735openalex-snapshot
Heterogeneous Photocatalysis in Microreactors for Efficient Reduction of Nitrobenzene to Aniline: Mechanisms and Energy Efficiency
inferred← citeshttps://doi.org/10.1002/chem.200801882openalex-snapshot
Mechanistic Study of the Palladium–Phenanthroline Catalyzed Carbonylation of Nitroarenes and Amines: Palladium–Carbonyl Intermediates and Bifunctional Effects
inferred← citeshttps://doi.org/10.1002/chem.200900281openalex-snapshot
Construction of Nitrogen‐Containing Heterocycles by CH Bond Functionalization
inferred← citeshttps://doi.org/10.1002/chem.201003621openalex-snapshot
Phosphane‐Free Green Protocol for Selective Nitro Reduction with an Iron‐Based Catalyst
inferred← citeshttps://doi.org/10.1002/chem.201404307openalex-snapshot
Silver Nanoparticles Supported on CeO2‐SBA‐15 by Microwave Irradiation Possess Metal–Support Interactions and Enhanced Catalytic Activity
inferred← citeshttps://doi.org/10.1002/chem.201404325openalex-snapshot
Photochemically Engineering the Metal–Semiconductor Interface for Room‐Temperature Transfer Hydrogenation of Nitroarenes with Formic Acid
inferred← citeshttps://doi.org/10.1002/chem.201501361openalex-snapshot
Color‐Controlled Ag Nanoparticles and Nanorods within Confined Mesopores: Microwave‐Assisted Rapid Synthesis and Application in Plasmonic Catalysis under Visible‐Light Irradiation
inferred← citeshttps://doi.org/10.1002/chem.201603626openalex-snapshot
Using Anilines as Masked Cross‐Coupling Partners: Design of a Telescoped Three‐Step Flow Diazotization, Iododediazotization, Cross‐Coupling Process
inferred← citeshttps://doi.org/10.1002/chem.201801942openalex-snapshot
Ultrafine FeCu Alloy Nanoparticles Magnetically Immobilized in Amine‐Rich Silica Spheres for Dehalogenation‐Proof Hydrogenation of Nitroarenes
inferred← citeshttps://doi.org/10.1002/chem.201801972openalex-snapshot
Metal‐Free Deoxygenation and Reductive Disilylation of Nitroarenes by Organosilicon Reducing Reagents
inferred← citeshttps://doi.org/10.1002/chem.202001329openalex-snapshot
Finely Controlled Platinum Nanoparticles over ZnO Nanorods for Selective Hydrogenation of 3‐Nitrostyrene to 3‐Vinylaniline
inferred← citeshttps://doi.org/10.1002/chem.202301978openalex-snapshot
Direct Synthesis of Unprotected Indolines Through Intramolecular sp3 C−H Amination Using Nitroarenes as Aryl Nitrene Precursors
inferred← citeshttps://doi.org/10.1002/chem.202402870openalex-snapshot
Visible‐Light‐Promoted Reduction of Nitroarenes with Formate Salts as Reductants
inferred← citeshttps://doi.org/10.1002/chin.199703321openalex-snapshot
ChemInform Abstract: Selective Catalytic Reduction of Aromatic Nitro Compounds into Aromatic Amines, Isocyanates, Carbamates, and Ureas Using CO
inferred← citeshttps://doi.org/10.1002/cjce.22822openalex-snapshot
Cu submicroparticles catalyzed reduction of 3‐nitro‐4‐methoxyacetanilide to 3‐amino‐4‐methoxyacetanilide in water
inferred← citeshttps://doi.org/10.1002/cjoc.20010191125openalex-snapshot
Palladium‐catalyzed carbonylation of primary amines in supercritical carbon dioxide
inferred← citeshttps://doi.org/10.1002/cjoc.20020200925openalex-snapshot
Samarium‐promoted Chemoselective Reduction of Aromatic Nitro Compounds in Ionic Liquid
inferred← citeshttps://doi.org/10.1002/cjoc.20030210303openalex-snapshot
Preparation of Aromatic Amines by Reduction of Aromatic Nitro Compounds with Metallic Tellurium in Near‐Critical Water
inferred← citeshttps://doi.org/10.1002/cjoc.200890256openalex-snapshot
Water as a Direct Hydrogen Donor in Supercritical Carbon Dioxide: A Novel and Efficient Zn‐H2O‐CO2 System for Chemo‐selective Reduction of Nitrobenzenes to Anilines
inferred← citeshttps://doi.org/10.1002/cjoc.201190117openalex-snapshot
Magnetically Separable and Versatile Pd/Fe3O4 Catalyst for Efficient Suzuki Cross‐Coupling Reaction and Selective Hydrogenation of Nitroarenes
inferred← citeshttps://doi.org/10.1002/cjoc.201600745openalex-snapshot
Important Green Chemistry and Catalysis: Non‐phosgene Syntheses of Isocyanates – Thermal Cracking Way
inferred← citeshttps://doi.org/10.1002/cjoc.70029openalex-snapshot
Light‐Promoted Synthesis of Arylamines from Nitro Compounds and Grignard Reagents
inferred← citeshttps://doi.org/10.1002/cplu.201800131openalex-snapshot
Application of Silicon‐Initiated Water Splitting for the Reduction of Organic Substrates
inferred← citeshttps://doi.org/10.1002/cssc.201402827openalex-snapshot
Methyl N‐Phenyl Carbamate Synthesis from Aniline and Methyl Formate: Carbon Recycling to Chemical Products
inferred← citeshttps://doi.org/10.1002/cssc.201600587openalex-snapshot
Iron‐Catalyzed Reaction of Urea with Alcohols and Amines: A Safe Alternative for the Synthesis of Primary Carbamates
inferred← citeshttps://doi.org/10.1002/cssc.201901535openalex-snapshot
Synergistic Effects of ppm Levels of Palladium on Natural Clinochlore for Reduction of Nitroarenes
inferred← citeshttps://doi.org/10.1002/cssc.202001085openalex-snapshot
Downstream Processing Strategies for Lignin‐First Biorefinery
inferred← citeshttps://doi.org/10.1002/cssc.202002073openalex-snapshot
Transition Metal‐Free Synthesis of Carbamates Using CO2 as the Carbon Source
inferred← citeshttps://doi.org/10.1002/ejic.202000012openalex-snapshot
Fe3O4@MOF Magnetic Nanocomposites: Synthesis and Applications
inferred← citeshttps://doi.org/10.1002/ejic.202200037openalex-snapshot
Tandem Pauson‐Khand Reaction Using Carbon Dioxide as the C1‐Source
inferred← citeshttps://doi.org/10.1002/ejic.202400157openalex-snapshot
Ni2MnAl Heusler Alloy Nanoparticles for Chemoselective Hydrogenation of Nitro Compounds
inferred← citeshttps://doi.org/10.1002/ejoc.200300127openalex-snapshot
Synthesis of N‐Phenyl‐N′‐pyrimidylurea Derivatives by Selenium‐ or Selenium Dioxide‐Catalyzed Reductive Carbonylation of Nitroaromatics
inferred← citeshttps://doi.org/10.1002/ejoc.201101784openalex-snapshot
Highly Efficient Synthesis of Ureas and Carbamates from Amides by Iodosylbenzene‐Induced Hofmann Rearrangement
inferred← citeshttps://doi.org/10.1002/ejoc.201600588openalex-snapshot
Palladium‐Catalyzed C–S Bond Formation of Stable Enamines with Arene/Alkanethiols: Highly Regioselective Synthesis of β‐Amino Sulfides
inferred← citeshttps://doi.org/10.1002/ejoc.201800581openalex-snapshot
Superparamagnetic Fe3O4 Nanoparticles in a Deep Eutectic Solvent: An Efficient and Recyclable Catalytic System for the Synthesis of Primary Carbamates and Monosubstituted Ureas
inferred← citeshttps://doi.org/10.1002/ejoc.201901140openalex-snapshot
A Fe3O4@SiO2/Schiff Base/Pd Complex as an Efficient Heterogeneous and Recyclable Nanocatalyst for One‐Pot Domino Synthesis of Carbamates and Unsymmetrical Ureas
inferred← citeshttps://doi.org/10.1002/ejoc.202100789openalex-snapshot
Synthesis of Indoles by Reductive Cyclization of Nitro Compounds Using Formate Esters as CO Surrogates
inferred← citeshttps://doi.org/10.1002/ejoc.202300904openalex-snapshot
Exhaustive Reduction of Esters, Carboxylic Acids and Carbamates to Methyl Groups Catalyzed by Boronic Acids
inferred← citeshttps://doi.org/10.1002/hlca.200790152openalex-snapshot
N‐Heterocyclic Carbene–Palladium Complexes as Efficient Catalysts for the Oxidative Carbonylation of Amines to Ureas
inferred← citeshttps://doi.org/10.1002/jccs.201400134openalex-snapshot
An Efficient Method for Chemoselective Reduction of Nitro Compounds Using Bimetallic Fe‐Ni NPs/H3PW12O40.×H2O System
inferred← citeshttps://doi.org/10.1002/open.201402006openalex-snapshot
Room Temperature, Metal‐Free Arylation of Aliphatic Alcohols
inferred← citeshttps://doi.org/10.1002/pc.27655openalex-snapshot
Three‐dimensional porous magnetic polyaniline supported Ag nanoparticles nanocomposites as an efficient and recyclable catalyst for nitrophenol reduction
inferred← citeshttps://doi.org/10.1002/slct.201601483openalex-snapshot
Deciphering Intermediates and Additives Effect on the Reduction of Nitrobenzene by SmI 2
inferred← citeshttps://doi.org/10.1002/slct.201601917openalex-snapshot
Copper‐Catalyzed Remote C−H Nitration of 8‐Amidoquinolines
inferred← citeshttps://doi.org/10.1002/slct.201700836openalex-snapshot
Palladium Nanoparticles Immobilized on Cross‐Linked Polymeric Ionic Liquid Material: Application as Efficient and Recoverable Catalyst for the Hydrogenation of Nitroarenes
inferred← citeshttps://doi.org/10.1002/slct.201701378openalex-snapshot
Cobalt Complexes Catalyze Reduction of Nitro Compounds: Mechanistic Studies
inferred← citeshttps://doi.org/10.1002/slct.201701693openalex-snapshot
Immobilizing Multifunctional Fe 2 O 3 ‐SnO 2 Nanoparticles to Carbon Nanospheres: An Extremely Active and Selective Catalyst for Hydrogen Transfer Reaction
inferred← citeshttps://doi.org/10.1002/slct.201801115openalex-snapshot
Molybdenum Carbide Catalysts for Chemoselective Transfer Hydrogenation of Nitroarenes
inferred← citeshttps://doi.org/10.1002/slct.201802977openalex-snapshot
Porous Triazine Containing Covalent Organic Polymer Supported Pd Nanoparticles: A Stable and Efficient Heterogeneous Catalyst for Sonogashira Cross‐Coupling and the Reduction of Nitroarenes
inferred← citeshttps://doi.org/10.1002/slct.201803566openalex-snapshot
A Versatile, Mild and Selective Reduction of Nitroarenes to Aminoarenes Catalyzed by CeO 2 Nanoparticles with Hydrazine Hydrate
inferred← citeshttps://doi.org/10.1002/slct.201803911openalex-snapshot
Mechanism of Direct Electrophilic Aromatic Amination: an Electrophile is Found by Quantum‐Chemical Study
inferred← citeshttps://doi.org/10.1002/slct.201902912openalex-snapshot
Generation of Anisotropic Au Nanostructures in Aqueous Carboxymethyl Cellulose Matrix for Potential Catalytic Application
inferred← citeshttps://doi.org/10.1002/slct.202300290openalex-snapshot
Access to Dihydroquinazolinones, spiro‐Quinazolinones and their Bioactive Molecular Scaffolds by Exploring the Unique Reactivity of 2‐Nitrobenzonitrile towards Cu‐Hydrazine Hydrate
inferred← citeshttps://doi.org/10.1002/slct.202405081openalex-snapshot
Perimidine‐2‐chalcogenone Ligand‐Supported Palladium(II) Complex: A Potent Catalyst in Suzuki–Miyuara Cross‐Coupling Reaction and Nitroarene Reduction
inferred← citeshttps://doi.org/10.1002/slct.202502763openalex-snapshot
Nickel‐Catalyzed Remote C(sp 2 )−H Nitration of 8‐Aminoquinolines Using AgNO 3 in Acetone
inferred← citeshttps://doi.org/10.1002/slct.74248openalex-snapshot
Total Synthesis of an Imidazole‐Fused Aaptamine Analogue via Sequential Ring Expansion and Palladium‐Catalyzed Carbonylative Annulation
inferred← citeshttps://doi.org/10.1002/zaac.202200340openalex-snapshot
Synthesis, characterization and catalytic activities of Zn(II) and Cd(II) complexes supported by unsymmetrical aryl thiourea ligands
inferred← citeshttps://doi.org/10.1006/jcat.2001.3350openalex-snapshot
A Novel PdCl2/ZrO2–SO2−4 Catalyst for Synthesis of Carbamates by Oxidative Carbonylation of Amines
inferred← citeshttps://doi.org/10.1007/978-3-030-20732-8_14openalex-snapshot
In Planta Synthesis of Nanomaterials for Environmental Remediation
inferred← citeshttps://doi.org/10.1007/978-3-319-30073-3_5openalex-snapshot
Catalytic Processes for Environmentally Friendly Methylene Diphenyl Diisocyanate Production
inferred← citeshttps://doi.org/10.1007/978-3-642-39016-6_9openalex-snapshot
The Reaction of C–NO2 with CO
inferred← citeshttps://doi.org/10.1007/s00339-021-05236-8openalex-snapshot
Pd(0)-impregnated SBA-15/melamine–formaldehyde nanocomposite: an efficient and reusable catalyst for reduction in nitroarenes
inferred← citeshttps://doi.org/10.1007/s00706-022-02932-wopenalex-snapshot
Efficient and heterogeneous transfer hydrogenation of nitroarenes using immobilized palladium nanoparticles on silica–starch substrate (PNP-SSS)
inferred← citeshttps://doi.org/10.1007/s00706-023-03131-xopenalex-snapshot
Synthesis of N-monosubstituted ureas in a mixture of choline chloride and aluminium nitrate as a simple, efficient, and selective process
inferred← citeshttps://doi.org/10.1007/s00706-025-03419-0openalex-snapshot
Efficient nitroarene reduction: innovative nickel immobilization on ZnFe₂O₄@EDTA nanocomposites
inferred← citeshttps://doi.org/10.1007/s00894-021-04914-xopenalex-snapshot
Intramolecular amination via acid-catalyzed rearrangement of azides: a potent alternative to intermolecular direct electrophilic route
inferred← citeshttps://doi.org/10.1007/s00894-026-06807-3openalex-snapshot
Pathological Pd-phenanthroline complex under standard DFT protocols
inferred← citeshttps://doi.org/10.1007/s10008-020-04526-0openalex-snapshot
Two-step one-pot electrosynthesis and catalytic activity of xCoO–yCo(OH)2-supported silver nanoparticles
inferred← citeshttps://doi.org/10.1007/s10008-022-05248-1openalex-snapshot
Electrosynthesis of nanocomposites of Ag, Au, Pd nanoparticles with aluminum(III), zinc(II), and titanium(IV) oxide-hydroxides
inferred← citeshttps://doi.org/10.1007/s10562-008-9764-2openalex-snapshot
Zinc Carboxylate Functionalized Mesoporous SBA-15 Catalyst for Selective Synthesis of Methyl-4,4′-di(phenylcarbamate)
inferred← citeshttps://doi.org/10.1007/s10562-009-0036-6openalex-snapshot
A Novel Transfer Hydrogenation with High Hydrogen Utilization for the Hydrogenation of Halogenated Nitrobenzene without Hydrodehalogenation
inferred← citeshttps://doi.org/10.1007/s10562-009-9930-1openalex-snapshot
Hydroformylation of Hex-1-ene by a Dinuclear gem-Dithiolato-bridged Rhodium Catalyst Under CO/H2O Conditions
inferred← citeshttps://doi.org/10.1007/s10562-013-1034-2openalex-snapshot
Nitrobenzene Hydrogenation on Au/TiO2 and Au/SiO2 Catalyst: Synthesis, Characterization and Catalytic Activity
inferred← citeshttps://doi.org/10.1007/s10562-014-1269-6openalex-snapshot
Iron and Palladium(II) Phthalocyanines as Recyclable Catalysts for Reduction of Nitroarenes
inferred← citeshttps://doi.org/10.1007/s10562-015-1531-6openalex-snapshot
Highly Selective and Efficient Reduction of Nitroarenes by Imidazolium Salt Stabilized Copper Nanoparticles in Aqueous Medium
inferred← citeshttps://doi.org/10.1007/s10562-015-1600-xopenalex-snapshot
Palladium Supported on Graphitic Carbon Nitride: An Efficient and Recyclable Heterogeneous Catalyst for Reduction of Nitroarenes and Suzuki Coupling Reaction
inferred← citeshttps://doi.org/10.1007/s10562-020-03244-6openalex-snapshot
MOF-Derived Cu-Nanoparticle Embedded in Porous Carbon for the Efficient Hydrogenation of Nitroaromatic Compounds
inferred← citeshttps://doi.org/10.1007/s10562-021-03793-4openalex-snapshot
Montmorillonite K30 Supported Tungstophosphoric Acid as an Efficient Catalyst for Condensation Reaction of Methyl N-phenylcarbamate for Generating Diurethane
inferred← citeshttps://doi.org/10.1007/s10562-025-05114-5openalex-snapshot
Cellulose-Tethered Triazine-Palladium Nanocatalyst for Carbon-Carbon Bond Formation Reaction and Nitroarene Reduction
inferred← citeshttps://doi.org/10.1007/s10570-018-1809-0openalex-snapshot
Cellulose supported bimetallic Fe–Cu nanoparticles: a magnetically recoverable nanocatalyst for quick reduction of nitroarenes to amines in water
inferred← citeshttps://doi.org/10.1007/s10870-008-9471-2openalex-snapshot
Synthesis and Crystal Structure of 1,3-Bis(p-nitrophenoxy)propane
inferred← citeshttps://doi.org/10.1007/s10904-023-02837-zopenalex-snapshot
Synthesis and Computational Studies of Novel Disulfide-Based Curing Cum Healing Agent for Self-healing Polyurethanes
inferred← citeshttps://doi.org/10.1007/s11030-023-10615-9openalex-snapshot
Environmentally benign synthesis of unsymmetrical ureas and their evaluation as potential HIV-1 protease inhibitors via a computational approach
inferred← citeshttps://doi.org/10.1007/s11144-021-02011-xopenalex-snapshot
Entangled nanofibrous copper: an efficient and high performance nanostructured catalyst in azide-alkyne cycloaddition reaction and reduction of nitroarenes and aromatic aldehydes
inferred← citeshttps://doi.org/10.1007/s11164-018-3621-8openalex-snapshot
Facile synthesis of monodispersed Pd nanocatalysts decorated on graphene oxide for reduction of nitroaromatics in aqueous solution
inferred← citeshttps://doi.org/10.1007/s11164-023-05139-8openalex-snapshot
A proficient catalytic reduction of nitroarenes and organic dyes using MOF-derived palladated nano-hydroxyapatite
inferred← citeshttps://doi.org/10.1007/s11172-020-2752-4openalex-snapshot
Two-step electrosynthesis and catalytic activity of CoO−CoO • xH2O-supported Ag, Au, and Pd nanoparticles
inferred← citeshttps://doi.org/10.1007/s11237-026-09876-wopenalex-snapshot
Influence of Composition of Nanosized MoS(2–x)Ox on Its Catalytic Properties in Bromoquinoline Hydrogenation Processes
inferred← citeshttps://doi.org/10.1007/s11244-014-0269-5openalex-snapshot
Selective Hydrogenation of 4-Nitrobenzaldehyde to 4-Aminobenzaldehyde by Colloidal RhCu Bimetallic Nanoparticles
inferred← citeshttps://doi.org/10.1007/s11696-016-0106-3openalex-snapshot
A photocatalytic green system for chemoselective reduction of nitroarenes
inferred← citeshttps://doi.org/10.1007/s11814-017-0192-0openalex-snapshot
Critical analysis of various supporting mediums employed for the incapacitation of silver nanomaterial for aniline and phenolic pollutants: A review
inferred← citeshttps://doi.org/10.1007/s12010-014-0831-4openalex-snapshot
Plant Extract: A Promising Biomatrix for Ecofriendly, Controlled Synthesis of Silver Nanoparticles
inferred← citeshttps://doi.org/10.1007/s12274-016-1080-3openalex-snapshot
Preparation of a magnetically recoverable nanocatalyst via cobalt-doped Fe3O4 nanoparticles and its application in the hydrogenation of nitroarenes
inferred← citeshttps://doi.org/10.1007/s12274-019-2439-zopenalex-snapshot
Single Pt atom decorated graphitic carbon nitride as an efficient photocatalyst for the hydrogenation of nitrobenzene into aniline
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