Gene A. HiegelCynthia B. Gilley2012-11-142025-02-172012-11-142012-11-14https://dl.ftveti.edu.et/handle/123456789/4060Primary 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 e.Primary 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 e.enPrimary alcohols; Methyl esters; Lactones; Diols; Oxidation; Synthesis; Preparation; Trichloroisocyanuric acid.Article