This article is cited in 9 papers

General regioselective synthesis of 2,2-disubstituted 3-hydroxyimidazolidin-4-ones

I. V. Vystorop^a, K. A. Lyssenko^b, V. N. Voznesensky^c, V. P. Lodygina^a, R. G. Kostyanovsky<sup>c

a</sup> 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 reactions of glycine hydroxamic acid with aliphatic ketones and acetophenone are commonly used for the regioselective synthesis of cyclic hydroxamic acids 6a–e; spiro hydroxamic acid 6a was structurally characterised by X-ray diffraction analysis.

Language: English

DOI: 10.1070/MC2002v012n05ABEH001657

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