Oxidation with Nickel Peroxide. III. Oxidative Cleavage of α-Glycols, α-Hydroxy Acids, α-Keto Alcohols, and α-Keto Acids.
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概要
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Solid nickel peroxide, readily obtainable by the treatment of nickel salts with sodium hypochlorite in alkaline solution, has been proved to be an useful reagent for the oxidative cleavage of α-glycols and α-hydroxy acids in aprotic solvents. Some kinds of aldehydes or ketones were obtained in moderately good yield as glycol cleavage products. With nickel peroxide in an aqueous alkaline solution, α-keto alcohols and α-keto acids were transformed into carboxylic acids by the oxidative cleavage.
- 公益社団法人日本薬学会の論文
- 1964-04-25
著者
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中川 国夫
徳島文理大
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杉田 実男
Shionogi Research Laboratory Shionogi & Co. Ltd.
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中川 国夫
Shionogi Research Laboratory, Shionogi & Co., Ltd.
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伊賀野 憲一
Shionogi Research Laboratory, Shionogi & Co., Ltd.
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伊賀野 憲一
Shionogi Research Laboratory Shionogi & Co. Ltd.
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- Oxidation with Nickel Peroxide. III. Oxidative Cleavage of α-Glycols, α-Hydroxy Acids, α-Keto Alcohols, and α-Keto Acids.
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