Oxidation of secondary alcohols to ketones - Wikipedia, the free encyclopedia
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The oxidation of secondary alcohols to ketones is an important oxidation reaction in organic chemistry. When a secondary alcohol is oxidised, it is converted to a ketone. The hydrogen from the hydro...
en.wikipedia.org/wiki/Oxidation_of_secondary_alcohols_t...
en.wikipedia.org/wiki/Oxidation_of_secondary_alcohols_to_ketones
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Alcohol - Wikipedia, the free encyclopedia
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In chemistry, an alcohol is any organic compound in which a hydroxyl group ( -OH ) is bound to a carbon atom of an alkyl or substituted alkyl group. An important group of alcohols is formed by the...
en.wikipedia.org/wiki/Alcohol
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A method for preparing an aldehyde or ketone by oxidizing a primary or secondary alcohol in the presence of a nitroxyl radical compound and a co-oxidant in an organic solvent, which process is characterized in using an organic N-bromoamide compound ... CATALYST SYSTEM FOR AEOROBIC OXIDATION OF PRIMARY AND SECONDARY ALCOHOLS.
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www.freepatentsonline.com/7208634.html
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Alkene oxides are produced in a continuous integrated two-,step process performed in liquid phase. Step I comprises the oxidation of a secondary alcohol with molecular oxygen to generate hydrogen pero ... 5,214,168 Zajacek and Crocco disclose an integrated process of air oxidation of an aryl-substituted secondary alcohol,
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www.freepatentsonline.com/6429323.html
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Mannitol dehydrogenases (MDH) are a family of Zn2+-independent long-chain alcohol dehydrogenases that catalyze the regiospecific NAD+-dependent oxidation of a secondary alcohol group in polyol substrates. ... Mario Klimacek and Bernd Nidetzky* ... Division of Biochemical Engineering, Institute of Food Technology,
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pubs.acs.org/doi/abs/10.1021/bi025517x
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An enantioselective asymmetric reduction of phenyl ring-containing prochiral ketones to yield the corresponding optically active secondary alcohols was achieved with W110A secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicus (W110A TESADH) in Tris buffer using 2-propanol (30%, v/v) as cosolvent...
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pubs.acs.org/doi/abs/10.1021/jo0616097
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What is claimed is: 1. A process for the selective oxidation of a primary or secondary alcohol to the corresponding aldehyde or ketone which comprises reacting said alcohol with a solutioncontaining an anhydride of the formula (RCO).sub.2 O and a trialkanoyl periodinane compound of formula I ##STR8##;
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www.patentgenius.com/patent/6762327.html
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*Stevens R, Chapman K, Weller H. 1980. Convenient and Inexpensive Procedure for Oxidation of; Secondary Alcohols to Ketones. J. Org. Chem; 45:2030-2032. The Original reaction: Hypochlorite Oxidation; Stevens R, Chapman K, Weller H. 1980. Convenient and Inexpensive Procedure for Oxidation of;
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www.marian.edu/chemphys/greenchem/BleachOxidation.pdf
www.marian.edu/chemphys/greenchem/BleachOxidation.pdf
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A rapid oxidation of primary and secondary alcohols using catalytic amounts of TEMPO and Yb(OTf)3 in combination with a stoichiometric amount of iodosylbenzene afforded carbonyl compounds in excellent yields without over-oxidation. ... Pd/C in aqueous alcohol with molecular oxygen, sodium borohydride,
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www.organic-chemistry.org/synthesis/C2O/ketones/oxidati...
www.organic-chemistry.org/synthesis/C2O/ketones/oxidationsalcohols.shtm
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