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Ketones homogeneous hydrogenation

Chiral ligands for homogeneous hydrogenation of olefins and ketones... [Pg.36]

N O Y O R I Chiral homogeneous hydrogenation Homogeneous chiral hydrogenation ol unsaluraled alcohols, or cartMxyNc acids, enamides, ketones in the presence ol BINAP Ru or Rh complex 8 as catalyst. [Pg.276]

The hydrogenation of 5a-cholestanone (58) in methanolic hydrobromic acid over platinum gives 3j5-methoxycholestane ° (61). This compound is also obtained from the palladium oxide reduction of (58) in methanol in the absence of acid. Hydrogenation of 5 -cholestanone also gives the 3j5-methoxy product under these conditions. Reduced palladium oxides are quite effective for the conversion of ketones to ethers. The use of aqueous ethanol as the solvent reduces the yield of ether. Ketals are formed on attempted homogeneous hydrogenation of a 3-keto group in methanol. ... [Pg.136]

The generally accepted mechanism of homogeneous hydrogenation of simple ketones seems to occur by a [7r2 + cr2] pathway as depicted in Scheme 16. [Pg.86]

The synthesis of cationic rhodium complexes constitutes another important contribution of the late 1960s. The preparation of cationic complexes of formula [Rh(diene)(PR3)2]+ was reported by several laboratories in the period 1968-1970 [17, 18]. Osborn and coworkers made the important discovery that these complexes, when treated with molecular hydrogen, yield [RhH2(PR3)2(S)2]+ (S = sol-vent). These rhodium(III) complexes function as homogeneous hydrogenation catalysts under mild conditions for the reduction of alkenes, dienes, alkynes, and ketones [17, 19]. Related complexes with chiral diphosphines have been very important in modern enantioselective catalytic hydrogenations (see Section 1.1.6). [Pg.10]

Until now, most studies on homogeneous hydrogenation by clusters have concentrated on alkenes and alkynes, though hopefully other substrates such as aldehydes, ketones, imines, and others will be further investigated, particularly using those systems that are now known to be genuine cluster catalysts. [Pg.213]

Homogeneous Hydrogenation of Aldehydes, Ketones, I mines and Carboxylic Acid Derivatives ... [Pg.413]

The Stereochemistry of Hydrogenation of , -Unsaturated Ketones Robert L. Augustine Asymmetric Homogeneous Hydrogenation J. D. Morrison, W. F. Masler, and M. K. Neuberg... [Pg.366]

Aqueous biphasic catalysis is also used in homogeneous hydrogenations.117-119 In new examples Ru clusters with the widely used TPPTN [tris(3-sulfonatophenyl) phosphine] ligand120 and Rh complexes with novel carboxylated phosphines121 were applied in alkene hydrogenation, whereas Ru catalysts were used in the hydro-genation of aromatics. Aerobic oxidation of terminal alkenes to methyl ketones was carried out in a biphasic liquid-liquid system by stable, recyclable, water-soluble Pd(II) complexes with sulfonated bidentate diamine ligands.124... [Pg.812]


See other pages where Ketones homogeneous hydrogenation is mentioned: [Pg.131]    [Pg.131]    [Pg.150]    [Pg.434]    [Pg.251]    [Pg.248]    [Pg.263]    [Pg.638]    [Pg.1073]    [Pg.1583]    [Pg.1611]    [Pg.363]    [Pg.74]    [Pg.55]    [Pg.59]    [Pg.119]    [Pg.119]    [Pg.77]   
See also in sourсe #XX -- [ Pg.56 ]

See also in sourсe #XX -- [ Pg.56 ]




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Homogeneous Catalysts and Ketone Hydrogenation

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Hydrogen homogeneous

Hydrogenation homogenous

Hydrogenation ketones

Ketones asymmetric homogeneous hydrogenation

Ketones hydrogen

Ketones hydrogenation, homogeneous catalysis

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