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Issue 12, 1984
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Selective oxidation of primary and secondary alcohols using di-isopropyl sulphide–N-chlorosuccinimide

Abstract

Di-isopropyl sulphide in combination with N-chlorosuccinimide at 0 ° oxidizes primary alcohols to aldehydes but does not oxidizes secondary alchols, whereas at –78 °C, the same reagent mixture oxidizes secondary alcohols to ketones but does not affect primary alcohols.

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Article type: Paper
DOI: 10.1039/C39840000762
Citation: J. Chem. Soc., Chem. Commun., 1984,0, 762-763

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    Selective oxidation of primary and secondary alcohols using di-isopropyl sulphide–N-chlorosuccinimide

    K. S. Kim, I. H. Cho, B. K. Yoo, Y. H. Song and C. S. Hahn, J. Chem. Soc., Chem. Commun., 1984, 0, 762
    DOI: 10.1039/C39840000762

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