Aerobic oxidation acid

Subsequent to the development of the (salen)Cr-catalyzed desymmetrization of meso-epoxides with azide (Scheme 7.3), Jacobsen discovered that the analogous (salen)Co(n) complex 6 promoted the enantioselective addition of benzoic acids to meso-epoxides to afford valuable monoprotected C2-symmetric diols (Scheme 7.15) [26], Under the reaction conditions, complex 6 served as a precatalyst for the (salen) Co(iii)-OBz complex, which was fonned in situ by aerobic oxidation. While the enantioselectivity was moderate for certain substrates, the high crystallinity of the products allowed access to enantiopure materials by simple recrystallization. 

The citric acid cycle is the final common pathway for the aerobic oxidation of carbohydrate, lipid, and protein because glucose, fatty acids, and most amino acids are metabolized to acetyl-CoA or intermediates of the cycle. It also has a central role in gluconeogenesis, lipogenesis, and interconversion of amino acids. Many of these processes occur in most tissues, but the hver is the only tissue in which all occur to a significant extent. The repercussions are therefore profound when, for example, large numbers of hepatic cells are damaged as in acute hepatitis or replaced by connective tissue (as in cirrhosis). Very few, if any, genetic abnormalities of citric acid cycle enzymes have been reported such ab-normahties would be incompatible with life or normal development. 

Identical kinetics are found for the uranyl ion-catalysed aerobic oxidation of ascorbic acid and a similar mechanism has been put forward These results and others afford a sequence of catalytic activity for the aerobic oxidation of ascorbic acid ... 

Bio-ethanol is attracting growing interests in relation to the shift of raw materials from petroleum to biomass. A pioneering work by Christensen is that over MgAl203 support gold is much more selective to acetic acid than palladium and platinum in the aerobic oxidation of ethanol in water in a batch reactor. Figure 32 shows that selectivity to acetic acid exceeds 80% [99]. In contrast, Au/Si02 catalysts prepared by deposition reduction... 

DuPont has developed a process for the manufacture of glyoxylic acid by aerobic oxidation of glycolic acid (Fig. 2.33) mediated by whole cells of a recombinant methylotrophic yeast (Gavagnan et al, 1995). The glycolic acid raw material is readily available from the acid-catalysed carbonylation of formaldehyde. Traditionally, glyoxylic acid was produced by nitric acid oxidation of acetaldehyde or glyoxal, processes with high E factors, and more recently by ozonolysis of maleic anhydride. 

Recently, great advancement has been made in the use of air and oxygen as the oxidant for the oxidation of alcohols in aqueous media. Both transition-metal catalysts and organocatalysts have been developed. Complexes of various transition-metals such as cobalt,31 copper [Cu(I) and Cu(II)],32 Fe(III),33 Co/Mn/Br-system,34 Ru(III and IV),35 and V0P04 2H20,36 have been used to catalyze aerobic oxidations of alcohols. Cu(I) complex-based catalytic aerobic oxidations provide a model of copper(I)-containing oxidase in nature.37 Palladium complexes such as water-soluble Pd-bathophenanthroline are selective catalysts for aerobic oxidation of a wide range of alcohols to aldehydes, ketones, and carboxylic acids in a biphasic... 

Aerobic oxidation of formaldehyde in water under mild conditions (20-40 °C, 1 atm of air or 02) in the presence of Ce-substituted POMs affords formic acid with high selectivity. 

The development of catalysts for the oxidation of organic compounds by air under ambient conditions is of both academic and practical importance (1). Formaldehyde is an important intermediate in synthetic chemistry as well as one of the major pollutants in the human environment (2). While high temperature (> 120 °C) catalytic oxidations are well known (3), low temperature aerobic oxidations under mild conditions have yet to be reported. Polyoxometalates (POMs) are attractive oxidation catalysts because these extensively modifiable metal oxide-like structures have high thermal and hydrolytic stability, tunable acid and redox properties, solubility in various media, etc. (4). Moreover, they can be deposited on fabrics and porous materials to render these materials catalytically decontaminating (5). Here we report the aerobic oxidation of formaldehyde in water under mild conditions (20-40 °C, 1 atm of air or 02) in the presence of Ce-substituted POMs (Ce-POMs). 

The aerobic oxidation of o-xylene to phthalic acid or anhydride at elevated temperatures is industrially important, and the flammability limits and explosion parameters at 350°C under a range of pressures have been redetermined. 

In liquid phase aerobic oxidation of p-xylene in acetic acid to terephthalic acid, it is important to eliminate the inherent hazards of this fuel-air mixture. Effects of temperature, pressure and presence of steam on the explosive limits of the mixture have been studied. 

Hydroxylamine is a powerful reducant, particularly when anhydrous, and if exposed to air on a fibrous extended surface (filter paper) it rapidly heats by aerobic oxidation. It explodes in contact with air above 70°C [1]. Barium peroxide will ignite aqueous hydroxylamine, while the solid ignites in dry contact with barium oxide, barium peroxide, lead dioxide and potassium permanganate, but with chlorates, bromates and perchlorates only when moistened with sulfuric acid. Contact of the anhydrous base with potassium dichromate or sodium dichromate is violently explosive, but less so with ammonium dichromate or chromium trioxide. Ignition occurs in gaseous chlorine, and vigorous oxidation occurs with hypochlorites. 

The supported Co2+-substituted Wells-Dawson POM, Cs6H2[P2W17061Co(OH2)], on silica was stable up to 773 K and catalyzed the heterogeneous oxidation of various aldehydes to the corresponding carboxylic acids with 02 as a sole oxidant [116], The H5PV2Mo10O40 POM, impregnated onto meso-porous MCM-41, catalyzed the aerobic oxidation of alkanes and alkenes using isobutyraldehyde as a... 

Present developments. One might think that an established reaction such as aerobic oxidation (or autoxidation) is not the subject of further research and improvement, but this is definitely not the case and both new homogeneous and heterogeneous catalysts are in development. In the introduction we already mentioned the drawbacks of oxidation of cyclohexene to adipic acid and several researchers address this challenge. Also a highly developed reaction such as the oxidation of paraxylene is subject to further improvements. 

Formation of benzoic acid has not been observed. These results clearly suggest that in the aerobic oxidation of neat ethylbenzene the cubane complexes cobalt(III) are involved as the catalytic species. 

In the aerobic oxidation of the non-activated aliphatic primary and secondary alcohols to the corresponding aldehydes and ketones, co-catalysts or other additives are normally required 223-226). The catalytic aerobic oxidation of aromatic aldehydes to the corresponding carboxylic acids with Ni(acac)2 in ionic liquids was the first example of an aerobic oxidation in ionic liquids 227). 

It has now been found that the quinones 13, 14 and 15 from the aerobic oxidation of veratryl alcohol by lignin peroxidase were also reduced by fungal mycelium to yield the corresponding hydroquinones. For quinone 14 this reduction had already been reported by Buswell et al. (17) in a study of vanillic acid metabolism. 

---