The oxidation of aldehydes to methyl esters using trichloroisocyanuric acid

Article abstract of DOI:10.1080/00397919608004579

Aldehydes are readily oxidized to methyl esters by a solution of methanol, pyridine, and trichloroisocyanuric acid in acetonitrile, acetone, or methylene chloride.

Full text of DOI:10.1080/00397919608004579

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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The Oxidation of Aldehydes
to Methyl Esters using
Trichloroisocyanuric Acid
a
a
Gene A. Hiegel , Christopher D. Bayne , Yariv
a
a
a
Donde , Gerald S. Tamashiro & Lisa A. Hilberath
a
Department of Chemistry and Biochemistry,
California State University, Fullerton, California,
92634
Published online: 21 Aug 2006.
To cite this article: Gene A. Hiegel , Christopher D. Bayne , Yariv Donde , Gerald S.
Tamashiro & Lisa A. Hilberath (1996): The Oxidation of Aldehydes to Methyl Esters
using Trichloroisocyanuric Acid, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 26:14, 2633-2639
To link to this article: http://dx.doi.org/10.1080/00397919608004579
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