Gene A. HiegelCynthia B. Gilley2012-11-152025-02-172012-11-152012-11-14https://dl.ftveti.edu.et/handle/123456789/4116Primary alcohols and diols are easily oxidized to methyl esters by a solutionof trichloroisocyanuric acid with methyl alcohol in dichloromethane. In addition, a,o-diols are also readily oxidized into lactones by refluxing with trichloroisocyanuric acid and pyridine indichloromethan ePrimary alcohols and diols are easily oxidized to methyl esters by a solutionof trichloroisocyanuric acid with methyl alcohol in dichloromethane. In addition, a,o-diols are also readily oxidized into lactones by refluxing with trichloroisocyanuric acid and pyridine indichloromethan eenPrimary alcohols; Methyl esters; Lactones; Diols; Oxidation; Synthesis; Preparation; Trichloroisocyanuric acidThe Oxidation of Primary Alcohols to Methyl Esters and Diols to Lactones Using Trichloroisocyanuric AcidArticle