The Oxidation of Primary Alcohols to Methyl Esters and Diols to Lactones Using Trichloroisocyanuric Acid

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dc.contributor.authorGene A. Hiegel
dc.contributor.authorCynthia B. Gilley
dc.date.accessioned2012-11-15T06:32:51Z
dc.date.accessioned2025-02-17T14:01:24Z
dc.date.available2012-11-15T06:32:51Z
dc.date.issued2012-11-14
dc.descriptionPrimary 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 een_US
dc.description.abstractPrimary 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 een_US
dc.identifier.urihttps://dl.ftveti.edu.et/handle/123456789/4116
dc.language.isoenen_US
dc.subjectPrimary alcohols; Methyl esters; Lactones; Diols; Oxidation; Synthesis; Preparation; Trichloroisocyanuric aciden_US
dc.titleThe Oxidation of Primary Alcohols to Methyl Esters and Diols to Lactones Using Trichloroisocyanuric Aciden_US
dc.typeArticleen_US

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