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

13Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.
Get full text

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free