Abstract
[Figure not available: see fulltext.] Arylglyoxal hydrates interact with N-alkoxyureas and N-hydroxyurea in acetic acid with selective formation of 3-alkoxy-5-arylimidazolidine-2,4-diones and 5-aryl-3-hydroxyimidazolidine-2,4-diones, respectively. The structures of 3-methoxy-5-phenylimidazolidine-2,4-dione, 3-ethoxy-5-phenylimidazolidine-2,4-dione, and 3-butoxy-5-(4-chlorophenyl)imidazolidine-2,4-dione were studied by X-ray structural analysis.
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Shtamburg, V. G., Shtamburg, V. V., Anishchenko, A. A., Zubatyuk, R. I., Mazepa, A. V., Klotz, E. A., … Kostyanovsky, R. G. (2015). Single-stage synthesis of 3-hydroxy- and 3-alkoxy-5-arylimidazolidine-2,4-diones by reaction of arylglyoxal hydrates with N-hydroxy- and N-alkoxyureas. Chemistry of Heterocyclic Compounds, 51(6), 553–559. https://doi.org/10.1007/s10593-015-1735-0
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