An improved method for the synthesis of 5-aryl-3-methyl-2-methylimino-1,3,4-oxadiazoles

Article abstract of DOI:10.1080/00397919208021073

5-Aryl-3-methyl-2-methylimino-1,3,4-oxadiazoles were prepared in 54-81% yields by the mercuric oxide-induced cyclizations of 1-aroyl-2,4,-dimethylthiosemicarbazides.

Full text of DOI:10.1080/00397919208021073

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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An Improved Method for the
Synthesis of 5-Aryl-3-methyl-2-
methylimino-1,3,4-Oxadiazoles
John M. Kane a & Michael A. Staeger a
a Marion Merrell Dow Research Institute, 2110 E.
Galbraith Road, Cincinnati, Ohio, 45215
Published online: 23 Sep 2006.
To cite this article: John M. Kane & Michael A. Staeger (1992) An Improved Method
for the Synthesis of 5-Aryl-3-methyl-2-methylimino-1,3,4-Oxadiazoles, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 22:1, 1-11, DOI: 10.1080/00397919208021073
To link to this article: http://dx.doi.org/10.1080/00397919208021073
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