1118067-55-2Relevant academic research and scientific papers
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
Shtamburg, Vasiliy G.,Shtamburg, Viktor V.,Anishchenko, Andrey A.,Zubatyuk, Roman I.,Mazepa, Aleksander V.,Klotz, Eugene A.,Kravchenko, Svetlana V.,Kostyanovsky, Remir G.
, p. 553 - 559 (2015)
[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 str
Synthesis and crystal structure of new imidazolidine-2,4-dione and imidazolidin-2-one derivatives
Shtamburg, Vasiliy G.,Anishchenko, Andrey A.,Shtamburg, Victor V.,Shishkin, Oleg V.,Zubatyuk, Roman I.,Mazepa, Alexander V.,Rakipov, Ildar M.,Kostyanovsky, Remir G.
, p. 102 - 104 (2008/12/20)
Arylglyoxals condense with N-hydroxyurea in water via intermediate formation of N-hydroxy-N-[hydroxy(aroyl)]methylureas and 3,4,5-trihydroxy-5-arylimidazolidin-2-ones to yield 3-hydroxy-5-aryl-imidazolidine-2,4-diones as end products; the 3,4,5-trihydroxy
