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Nitro-reduction

Benzo[b]furan, 2-nitro-reduction, 4, 74, 647 Benzo[b]furan, 5-nitro-mass spectrometry, 4, 583 Benzo[b]furan, 2-(4-nitrophenyl)-properties, 4, 708 Benzo[b]furan, 2-phenyl-bromination, 4, 605 chloromethylation, 4, 607 nitration, 4, 604 photochemical reactions, 4, 636 properties, 4, 697 Benzo[b]furan, 3-phenyl-synthesis, 4, 697... [Pg.547]

Benzo[6]thiophene, 4-N-methylcarbamoyl-biological activity, 4, 913 Benzo[6]thiophene, 2-methyl-3-vinyl-cycloaddition reactions, 4, 795 Benzo[fc]thiophene, 2-( 1 -naphthyl)-synthesis, 4, 915 Benzo[6]thiophene, 2-nitro-reduction, 4, 815 synthesis, 4, 923 Benzo[6]thiophene, 3-nitro-cycloaddition reactions, 4, 789 Benzo[6]thiophene, 4-nitro-synthesis, 4, 923 Benzo[6]thiophene, 5-nitro-synthesis, 4, 923... [Pg.560]

Coumarin, 4-methyl-7-methoxy-mass spectra, 3, 608 Coumarin, 4-methylsulfonylmethyl-synthesis, 3, 805 Coumarin, nitro-reduction, 3, 691 Coumarin, 3-nitro methylation, 3, 682 Coumarin, 3-phenoxy-synthesis, 3, 807... [Pg.586]

Dibenzo[6,/][l,4]selenazocine, N-formyl-6,11-dihydro-synthesis, 6, 34l Dibenzoselenophene, 2-amino-diazotization, 4, 951 Dibenzoselenophene, 2-nitro-reduction, 4, 951 Dibenzoselenophene, 3-nitro-5-oxide... [Pg.602]

Pyridinium salts, 4-methoxy-l-methyl-3-nitro-reduction... [Pg.795]

Pyrimidine-4(3H)-thione, 6-methoxy-5-nitro-reduction, 3, 88 Pyrimidinethiones acidic pK, 3, 60 S-acylation, 3, 95 N-alkylated synthesis, 3, 139 aminolysis, 3, 94 desulfurization, 3, 93 electrophilic reactions, 3, 69 hydrolysis, 3, 94 oxidation, 3, 94, 138 pyrimidinone synthesis from, 3, 133 reactions... [Pg.808]

Pyrrole, 2-aeetyl-l-(2-hydroxyethyl)-5-nitro-cyelization, 4, 74 ipso substitution, 4, 243 Pyrrole, 2-aeetyl-l-methyl-dipole moment, 4, 194 photocyelization reaetions with 2,3-dimethylbut-2-ene, 4, 269 Pyrrole, 3-acetyl-4-methyl-Vilsmeier-Haaek formylation, 4, 222 Pyrrole, 2-aeetyl-3-nitro-reduction, 4, 297 Pyrrole, aeyl-basicity, 4, 207 isomerization, 4, 208 oximes... [Pg.813]

Saccharin, 2-methyl-reduction, 6, 152 Saccharin, 6-nitro-reduction, 6, 154 Saccharin, thio-hydrolysis, 6, 161 methylation, 6, 160 Safranines applications, 3, 196 Safrole derivatives toxicity, 1, 139-140 occurrence, 6, 781 Safrole, 1-hydroxy-toxicity, 1, 140 Salazosulfapyridine... [Pg.838]

Raney-nickel nitro reductions were reported for 3-nitro-l,X-naph-thyridin-4(lH)-ones (X = 5, 6, 7, and 8) (134a-134d), yielding 3-amino-4(lH)-ones, isolated as their hydrochlorides (135a-135d). [Pg.316]

Dinitroaniline herbicides show minimal plant systematic translocation properties with the majority of the absorbed residues in the root tissues. Metabolites identified include traces of Al-dealkylation, alkyl and aryl hydroxylation and nitro reduction products. Low levels of dinitroaniline herbicide residues have been reported in raw agricultural commodities according to Good Agricultural Practice. [Pg.389]

The fate of the dinitroaniline herbicides in soil is extremely complex and many metabolites have been identified. Golab and Althaus reported 28 metabolites identified in a degradation study of trifluralin in soil. Major degradation products of dinitroaniline herbicides were formed by nitro reduction, A-dealkylation (mono-dealkylated and completely dealkylated) and the ring formation of benzimidazole. [Pg.397]

Large-Scale Synthesis of Thienobenzazepine Derivatives Using Two Efficient Metal Catalyzed Processes Telescoped Nitro Reduction and Intramolecular Aminocarbonylation... [Pg.62]

See other catalytic nitro reduction processes, hydrogenation incidents See related nitroalkanes... [Pg.556]

See Other CATALYTIC NITRO REDUCTION PROCESSES, HYDROGENATION INCIDENTS, ORGANIC AZIDES... [Pg.633]

See other N-o compounds, catalytic nitro reduction processes... [Pg.733]

Catalytic hydrogenation on 400 g scale at 34 bar under excessively vigorous conditions (250°C, 12% catalyst, no solvent) caused the thin autoclave without bursting disk to rupture [1]. Under more appropriate conditions the hydrogenation is safe [2], See other catalytic nitro reduction processes... [Pg.912]

Reductions Epoxide hydroplase Azo and nitro reduction Carbonyl reductase Disulfide reduction Sulfoxide reduction Quinone reduction Reductive dehalogenation Microsomes, cytosol Gut microflora Cytosol Cytosol Cytosol Cytosol, microsomes Microsomes... [Pg.707]

Dinitrobenzene is an intermediate employed in chemical syntheses of a large number of compounds used in the dye, explosives and plastics industry. The compound is known to induce methemoglobinemia and to cause testicular toxicity with the Sertoli cell being the major target. Nitro reduction was observed in erythrocytes, in rat Sertoli-germ cell cocultures and in rat testicular subcellular fractions, and it was shown that 3-nitrosonitrobenzene was formed that was considerably more toxic. Testicular toxicity was enhanced when the intracellular thiol levels were reduced by pretreatment with diethylmaleate. In turn, pretreatment with cysteamine or ascorbate reduced the toxicity of 1,3-dinitrobenzene and 3-nitrosonitrobenzene. [Pg.1028]

CATALYTIC NITRO REDUCTION PROCESSES HYDROGENATION CATALYSTS HYDROGENATION INCIDENTS... [Pg.81]

CATALYTIC NITRO REDUCTION PROCESSES RN02 - RNH2... [Pg.82]

AGITATION INCIDENTS, AMINATION INCIDENTS, CATALYTIC NITRO REDUCTION PROCESSES... [Pg.412]

In contrast to the aforementioned monosubstitutions, much less is known about the effect of disubstitution. It appears that such benzamides are resistant to hydrolysis. The metabolic fate of nitromide (3,5-dinitrobenzamide, 4.63), a chicken-feed additive for the prevention of coccidosis, was investigated in rats. The metabolite 3-amino-5-nitrobenzoic acid (4.64), formed by ni-tro reduction and hydrolysis, was excreted in only trace amounts. Nitromide was metabolized mainly via nitro reduction [36], Similarly, no hydrolysis was... [Pg.117]


See other pages where Nitro-reduction is mentioned: [Pg.270]    [Pg.510]    [Pg.542]    [Pg.542]    [Pg.559]    [Pg.580]    [Pg.583]    [Pg.676]    [Pg.688]    [Pg.772]    [Pg.780]    [Pg.795]    [Pg.795]    [Pg.913]    [Pg.917]    [Pg.34]    [Pg.178]    [Pg.217]    [Pg.1025]    [Pg.198]    [Pg.124]    [Pg.224]    [Pg.315]    [Pg.343]    [Pg.346]   
See also in sourсe #XX -- [ Pg.229 ]

See also in sourсe #XX -- [ Pg.229 ]




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2- Nitro-5- furan, reduction

2.6- dinitrotoluene, nitro group reduction

4-Chloro-8-nitro-1.6-naphthyridine, reduction

4-Chloro-8-nitro-1.6-naphthyridine, reduction chloride

8-Nitro pyridine, from reduction

Acetophenone nitro-substituted, reduction

Alcohols, 2-nitro reductive denitration

Aldehydes, nitro, reduction

Aliphatic nitro compounds, reductions, lithium aluminum

Allyl nitro compounds reduction

Allylic nitro compounds, reduction

Amide cleavage induced by nitro group reduction

Amines By reduction of nitro compounds

Amino group nitro reduction

Ammonium chloride nitro compound reduction

Ammonium sulfide nitro group reduction

Aprotic solvents nitro compound reduction

Aromatic Amines and Other Reduction Products of Nitro Compounds

Aromatic nitro compounds reduction to hydroxylamines

Aromatic nitro compounds reduction with tin and hvdrochloric

Aromatic nitro group, reduction

Asymmetric reduction of 2-bromo(3-nitro-4-benzyloxy)acetophenone

Benzo furan 2- nitro-, reduction

CATALYTIC NITRO REDUCTION

CATALYTIC NITRO REDUCTION PROCESSES

Carbonyl compounds, from nitro reductive amination

Complex hydride reduction nitro compounds

Copper salts reduction, aromatic nitro compounds

Cyclization, reductive, aromatic nitro

Cyclohexane nitro-, reduction

Drug metabolism nitro reduction

Electrochemical reduction nitro compounds

Enzymes nitro compound reduction

For reduction of nitro compounds

Formic acid hydrogenation, nitro compound reduction

Heterocyclic compounds hydrogenation, nitro compound reduction

Hydrogen sulfide reduction, aromatic nitro compounds

Hydrogenation nitro reduction

Intermediate products in the reduction of nitro compounds

Ketones, nitro, reduction

NTERMEDIATE PRODUCTS IN THE REDUCTION OF NITRO COMPOUNDS

Nickel boride aliphatic nitro compound reduction

Nickel chloride aliphatic nitro compound reduction

Nitro acids, reduction

Nitro alcohols reduction

Nitro aldehydes, aromatic, reduction

Nitro aldehydes, aromatic, reduction preparation

Nitro aliphatic, reduction

Nitro alkene Enantioselective reduction

Nitro amides, reduction

Nitro amine oxides, reduction

Nitro amines reduction

Nitro azides, reduction

Nitro compds reductive

Nitro compounds aliphatic, reduction

Nitro compounds aromatic, reduction

Nitro compounds halogen-substituted aromatic, reduction

Nitro compounds intermediate products in reduction

Nitro compounds partial reduction

Nitro compounds poly-, reduction

Nitro compounds reduction

Nitro compounds reduction of, to amines

Nitro compounds reduction with aluminum amalgam

Nitro compounds reduction with ammonium formate

Nitro compounds reductive alkylation

Nitro compounds reductive cyclizations

Nitro compounds, aromatic, reductive

Nitro compounds, aromatic, reductive cyclization with triethyl phosphite

Nitro compounds, detection reduction

Nitro compounds, free-radical reduction

Nitro compounds, heterogeneous hydrogenation reduction reactions

Nitro compounds, reductive

Nitro compounds, reductive transformations

Nitro esters, reduction

Nitro group polarographic reduction

Nitro group reduction

Nitro groups, reduction aldehydes

Nitro groups, reduction amines

Nitro groups, reduction disulfides

Nitro groups, reduction esters

Nitro groups, reduction oximes

Nitro groups, reduction sulfonic acids

Nitro groups, substituted benzenes reduction

Nitro nitriles, reduction

Nitro reduction with

Nitro reduction, partial

Nitro reductive carbonylation

Nitro reductive ring fission

Nitro, acids Reduction products

Nitro-1,5 naphthyridines reduction

Nitro-aromatic compounds reduction potential effect

Nitro-azoxy reductive

Nitro-azoxy reductive transformation

Nitro-hydrocarbons reduction

Nitro-ketones, reduction with zinc

Nitrogen-containing compounds nitro group reduction

Nitroso compounds hydrogenation, nitro compound reduction

Nitroso compounds via nitro compound reduction

Olefinic nitro compounds, reduction

Parathion nitro reduction

Phosphorus reduction, nitro compounds

Reaction Reduction of a Nitro-Compound to an Amine

Reduction of Nitro Compounds into Amines

Reduction of Nitro and Nitroso Compounds

Reduction of Nitro and Nitrosoarenes

Reduction of Nitro- to Amino-groups

Reduction of a nitro

Reduction of a nitro compound to an amine

Reduction of aromatic nitro compound

Reduction of aromatic nitro groups

Reduction of aryl nitro compound

Reduction of carbonyl and nitro functionalities

Reduction of nitro

Reduction of nitro compounds

Reduction of nitro compounds and oximes to hydroxylamines

Reduction of nitro groups

Reduction reaction nitro groups

Reduction, azobenzenes nitro-compounds

Reductions nitro groups, palladium®) acetate

Reductions of Heterocyclic N-Oxides and Aromatic Nitro Groups

Reductive cyclization nitro ketones

Reductive cyclization of aromatic nitro

Reductive of nitro derivatives

Steroids, nitro reduction

The reduction of nitro compounds

Tin reduction of nitro groups

Titanium compounds aliphatic nitro compound reduction

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