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JOURNALS // Mendeleev Communications // Archive

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. 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.

Language: English

DOI: 10.1070/MC2003v013n03ABEH001790



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