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- W2950936148 abstract "Hydroxylation was shown to occur readily in the reactions of aromatic compounds such as benzoic acid, nitrobenzene, acetanilide, and phenol with ferrous ion-molecular oxygen in 0.5 M phosphate buffer (pH 6.8) at 40°C for 3 h. The yields of hydroxylated products were higher than those obtained with other reported hydroxylation systems of transition metalmolecular oxygen. The NIH shift was not observed in the title reactions of C (4)-deuterioacetanilide and C (4)-deuteriobenzoic acid. This system was also demonstrated to oxygenate caproic acid to give a mixture of 3-, 4-, and 5-oxocaproic acids in 67% total yield." @default.
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- W2950936148 date "1983-08-09" @default.
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- W2950936148 title "ChemInform Abstract: ON THE OXYGENATION OF SEVERAL AROMATIC AND ALIPHATIC COMPOUNDS WITH AQUEOUS FERROUS ION-MOLECULAR OXYGEN" @default.
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- W2950936148 doi "https://doi.org/10.1002/chin.198332115" @default.
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