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- W2056595001 abstract "1) The t-butyl chromate oxidation of myrtenol gave no ester, but it did give the corresponding aldehyde as the main product, while the oxidation of cyclohexylcarbinol gave a mixture of the corresponding aldehyde, acid and ester in comparable yields. 2) A similar oxidation of cyclohexanol afforded the corresponding ketone in a high yield, while the oxidation of cyclohexane-trans-1,2-diol produced no corresponding diketone, but it did produce the glycol fission product and a cyclic ester such as trans-1,2-adipoxycyclohexane (a new compound). On the other hand, p-menthane-trans-3,4-diol yielded only the corresponding hydroxyketone in a good yield." @default.
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- W2056595001 date "1965-09-01" @default.
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- W2056595001 title "Oxidation of Alcohols witht-Butyl Chromate. III. The Oxidation of Alicyclic Alcohols" @default.
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- W2056595001 doi "https://doi.org/10.1246/bcsj.38.1503" @default.
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