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This article is cited in 5 scientific papers (total in 5 papers)
2-Phenyl-3-hydroxyimidazolidin-4-one: the regioselective synthesis, structure and enantiomerically enriched crystallization
I. V. Vystoropa, K. A. Lyssenkob, R. G. Kostyanovskyc a Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation
b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
c N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation
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.
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
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