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Platinum-rhodium oxide, hydrogenation ketones

Reductions with platinum rhodium oxide Ring hydrogenation Sec. alcohols from ketones... [Pg.296]

Ruthenium is commonly used with other platinum metals as a catalyst for oxidations, hydrogenations, isomerizations, and reforming reactions. The synergetic effect of mixing ruthenium with catalysts of platinum, palladium, and rhodium lias been found for the hydrogenations of aromatic and aliphatic nitro compounds, ketones, pyndine, and nitriles. [Pg.1453]

The platinum catalyzed oxidation of alcohols with molecular oxygen has been known for a long time.52,53 Palladium and iridium are also effective for this reaction but not rhodium or ruthenium.54 The reaction proceeds by the initial dehydrogenation of the alcohol to produce the aldehyde or ketone with the adsorbed hydrogen then reacting with the oxygen to give water.53>55-58 These... [Pg.559]

The benzylic position of an alkylbcnzene can be brominated by reaction with jV-bromosuccinimide, and the entire side chain can be degraded to a carboxyl group by oxidation with aqueous KMnCfy Although aromatic rings are less reactive than isolated alkene double bonds, they can be reduced to cyclohexanes by hydrogenation over a platinum or rhodium catalyst. In addition, aryl alkyl ketones are reduced to alkylbenzenes by hydrogenation over a platinum catalyst. [Pg.587]

Reduction of carbocyclic rings in aromatic ketones can be accomplished by catalytic hydrogenation over platinum oxide or rhodium-platinum oxide and takes place only after the reduction of the carbonyl group, either to the alcoholic group, or to a methylene group [5S]. [Pg.113]

Enones are reduced to saturated ketones by catalytic hydrogenation provided the reaction is stopped following the absorption of 1 mol of hydrogen. " A number of catalysts were found useful for this, including platinum, platinum oxide,Pt/C, " Pd/C, - Rh/C, " tris(triphenylphosphine)rhodium chloride, - nickel-aluminum alloy in 10% aqueous NaOH, and zinc-reduced nickel in an aqueous medium. Mesityl oxide is formed from acetone and reduced in a single pot to methyl isobutyl ketone using a bifunctional catalyst which comprised palladium and zirconium phosphate (Scheme 20). [Pg.533]

Because oxidations with oxygen are free-radical reactions, free radicals should be good initiators. Indeed, in the presence of hydrogen bromide at high enough temperatures, lower molecular weight alkanes are oxidized to alcohols, ketones, or acids [5 7]. Much more practical are oxidations catalyzed by transition metals, such as platinum [5, 6, 55, 56], or, more often, metal oxides and salts, especially salts soluble in organic solvents (acetates, acetylacetonates, etc.). The favored catalysts are vanadium pent-oxide [3] and chlorides or acetates of copper [2, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66], iron [67], cobalt [68, 69], palladium [60, 70], rhodium [10], iridium [10], and platinum [5, 6, 56, 57]. [Pg.4]

Among the most significant developments in the field of catalysis in recent years have been the discovery and elucidation of various new, and often novel, catalytic reactions of transition metal ions and coordination compounds 13, 34). Examples of such reactions are the hydrogenation of olefins catalyzed by complexes of ruthenium (36), rhodium (61), cobalt (52), platinum (3, 26, 81), and other metals the hydroformylation of olefins catalyzed by complexes of cobalt or rhodium (Oxo process) (6, 46, 62) the dimerization of ethylene (i, 23) and polymerization of dienes (15, 64, 65) catalyzed by complexes of rhodium double-bond migration in olefins catalyzed by complexes of rhodium (24,42), palladium (42), cobalt (67), platinum (3, 5, 26, 81), and other metals (27) the oxidation of olefins to aldehydes, ketones, and vinyl esters, catalyzed by palladium chloride (Wacker process) (47, 48, 49,... [Pg.1]

Carbonyl groups. Breitner et al. found Engelhard Ru-C and Rh-C distinctly superior to Pl-C and Pd-C for the hydrogenation of ketones in neutral or basic medium. Hu.sek et til. iittcmpted reduction of tetramothy 1-1,3-cyclobutanedione with platinum, palladium, and rhodium catalysts but the results were very poor. With copper-chromium oxide and supported nickel culitlyilR yieldsol diols were moderate,... [Pg.1225]

Ruthenium-on-carbon in aqueous ethanol or platinum oxide also is used but to a much lesser extent than Pd. Palladium shows a low activity for hydrogenation of nonactivated aliphatic ketones, but all the platinum metals can be used in addition to Cu chromite and Ni catalysts. Platinum catalysts have been widely used, platinum-on-carbon in aqueous acid is satisfactory. Rhodium is active under mild conditions and leads to a-hydroxy steroids in excellent yields ... [Pg.255]


See other pages where Platinum-rhodium oxide, hydrogenation ketones is mentioned: [Pg.107]    [Pg.232]    [Pg.75]    [Pg.109]    [Pg.247]    [Pg.440]    [Pg.632]    [Pg.141]    [Pg.141]    [Pg.587]    [Pg.98]    [Pg.267]   
See also in sourсe #XX -- [ Pg.107 , Pg.109 , Pg.191 ]




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Hydrogen platinum

Hydrogenation ketones

Ketones hydrogen

Ketones oxidant

Ketones oxidation

Oxidation platinum

Oxidative ketones

Oxidative ketonization

Platinum hydrogenation

Platinum ketone hydrogenation

Platinum oxide

Platinum-rhodium oxide, hydrogenation

Rhodium ketones

Rhodium oxidation

Rhodium-platinum oxide

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