Abstract:
The reaction of glycine hydroxamic acid with benzaldehyde regioselectively affords the title racemic cyclic hydroxamic acid, which crystallises as enantiomorphic crystals (space group P212121) from a methanol solution.
Document Type:
Article
Language: English
Citation:
I. V. Vystorop, K. A. Lyssenko, R. G. Kostyanovsky, “2-Phenyl-3-hydroxyimidazolidin-4-one: the regioselective synthesis, structure and enantiomerically enriched crystallization”, Mendeleev Commun., 13:3 (2003), 116–118
Linking options:
https://www.mathnet.ru/eng/mendc3981
https://www.mathnet.ru/eng/mendc/v13/i3/p116
This publication is cited in the following 5 articles:
S. A. Goncharova, I. V. Vystorop, T. A. Raevskaya, N. P. Konovalova, “The Effectiveness of Cyclic Hydroxamic Acid CHA-5 against Drug-Resistant P388 Leukemia Strains”, Bull Exp Biol Med, 163:3 (2017), 385
Vasiliy G. Shtamburg, Viktor V. Shtamburg, Andrey A. Anishchenko, Roman I. Zubatyuk, Aleksander V. Mazepa, Eugene A. Klotz, Svetlana V. Kravchenko, Remir G. Kostyanovsky, “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”, Chem Heterocycl Comp, 51:6 (2015), 553
I. V. Vystorop, Yu. V. Nelyubina, V. N. Voznesensky, W.-H. Sun, V. P. Lodygina, K. A. Lyssenko, R. G. Kostyanovsky, “General regioselective synthesis and crystal structure of racemic 5-substituted 2,2-dimethyl-3-hydroxyimidazolidin-4-ones”, Mendeleev Commun., 20:2 (2010), 106–108
V. G. Shtamburg, A. A. Anishchenko, V. V. Shtamburg, O. V. Shishkin, R. I. Zubatyuk, A. V. Mazepa, E. M. Rakipov, R. G. Kostyanovsky, “Synthesis and crystal structure of new imidazolidine-2,4-dione and imidazolidin-2-one derivatives”, Mendeleev Commun., 18:2 (2008), 102–104
Joana Dumčiūtė, Vytas Martynaitis, Wolfgang Holzer, Sven Mangelinckx, Norbert De Kimpe, Algirdas Šačkus, “Synthesis and ring transformations of 1-amino-1,2,3,9a-tetrahydroimidazo[1,2-a]indol-2(9H)-ones”, Tetrahedron, 62:14 (2006), 3309
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