Mendeleev Commun., 2003 Volume 13, Issue 3, Pages 116–118
(Mi mendc3981)
This article is cited in
5 papers
2-Phenyl-3-hydroxyimidazolidin-4-one: the regioselective synthesis, structure and enantiomerically enriched crystallization
I. V. Vystorop a ,
K. A. Lyssenko b ,
R. G. Kostyanovsky c 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
P 2
1 2
1 2
1 ) from a methanol solution.
Language: English
DOI:
10.1070/MC2003v013n03ABEH001790
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