Аннотация:
The condensation of glycine hydroxamic acid with acetone regioselectively leads to the formation of the title achiral cyclic hydroxamic acid, which crystallises from an acetone solution as chiral crystals (space group P212121) of (P,1R,3S) and (M,1S,3R) enantiomers.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
I. V. Vystorop, K. A. Lyssenko, R. G. Kostyanovsky, “3-Hydroxy-2,2-dimethylimidazolidin-4-one: the regioselective synthesis and chiral crystallization”, Mendeleev Commun., 12:3 (2002), 85–87
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4104
https://www.mathnet.ru/rus/mendc/v12/i3/p85
Эта публикация цитируется в следующих 12 статьяx:
I. V. Vystorop, G. V. Shilov, A. V. Chernyak, E. N. Klimanova, T. E. Sashenkova, S. G. Klochkov, M. E. Neganova, Yu. R. Aleksandrova, U. Yu. Allayarova, D. V. Mishchenko, “Regioselective Synthesis, Structure, and Chemosensitizing Antitumor Activity of Cyclic Hydroxamic Acid Based on DL-Valine”, Russ J Bioorg Chem, 47:3 (2021), 757
I. V. Vystorop, N. P. Konovalova, Yu. V. Nelyubina, A. V. Chernyak, T. E. Sashenkova, E. N. Klimanova, A. N. Utienyshev, B. S. Fedorov, G. V. Shilov, R. G. Kostyanovsky, “Cyclic hydroxamic acids derived from α-amino acids 2. Regioselective synthesis, crystal structure, and antitumor activity of spiropiperidine-imidazolidine hydroxamic acids based on glycine and dl-alanine”, Russ Chem Bull, 62:5 (2013), 1272
Vytas Martynaitis, Rasa Steponavičiūtė, Sonata Krikštolaitytė, Joana Solovjova, Sven Mangelinckx, Norbert De Kimpe, Wolfgang Holzer, Algirdas Šačkus, “Synthesis and reactions of 1-hydroxy-9,9a-dihydro-1H-imidazo[1,2-a]indol-2-(3H)-ones”, Tetrahedron, 67:21 (2011), 3945
I. V. Vystorop, N. P. Konovalova, T. E. Sashenkova, E. N. Berseneva, A. V. Chernyak, B. S. Fedorov, R. G. Kostyanovsky, “1-Hydroxy-8-methyl-1,4,8-triazaspiro[4.5]decan-2-one and its (±)-3-methyl homologue: regioselective synthesis and in vivo evaluation as adjuvants in leukemia chemotherapy”, Mendeleev Commun., 21:5 (2011), 239–241
I. V. Vystorop, N. P. Konovalova, Yu. V. Nelyubina, V. N. Varfolomeev, B. S. Fedorov, T. E. Sashenkova, E. N. Berseneva, K. A. Lyssenko, R. G. Kostyanovsky, “Cyclic hydroxamic acids derived from α-amino acids 1. Regioselective synthesis, structure, NO-donor and antimetastatic activities of spirobicyclic hydroxamic acids derived from glycine and DL-alanine”, Russ Chem Bull, 59:1 (2010), 127
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
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
Igor V. Vystorop, Konstantin A. Lyssenko, Remir G. Kostyanovsky, “3‐Hydroxy‐2,2‐dimethylimidazolidin‐4‐one: The Regioselective Synthesis and Chiral Crystallization.”, ChemInform, 33:46 (2002), 141
I. V. Vystorop, K. A. Lyssenko, V. N. Voznesensky, V. P. Lodygina, R. G. Kostyanovsky, “General regioselective synthesis of 2,2-disubstituted 3-hydroxyimidazolidin-4-ones”, Mendeleev Commun., 12:5 (2002), 193–196
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