Abstract
A number of alcohols were oxidized to the corresponding carbonyl compounds in excellent yields using tetramethylammonium fluorochromate in acetic acid. The oxidant takes up two electrons, the reaction follows first-order kinetics with respect to the oxidant under pseudofirst-order conditions, and the concentration of alcohols changes according to the Michaelis-Menten dependence.
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Translated from Zhurnal Obshchei Khimii, Vol. 75, No. 12, 2005, pp. 1975–1977.
Original Russian Text Copyright © 2005 by Sadeghy, Ghammami.
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Sadeghy, B., Ghammami, S. Oxidation of Alcohols with Tetramethylammonium Fluorochromate in Aceticoi Acid. Russ J Gen Chem 75, 1886–1888 (2005). https://doi.org/10.1007/s11176-006-0008-0
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DOI: https://doi.org/10.1007/s11176-006-0008-0