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