Issue 5, 2002
From the journal:

Mendeleev Communications

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

Igor V. Vystorop,*a   Konstantin A. Lyssenko,b   Vladimir N. Voznesensky,c   Vera P. Lodyginaa  and  Remir G. Kostyanovskyc  

* Corresponding authors

a Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation, Chernogolovka, Noginsky district, Moscow Region, Russian Federation
E-mail: vystorop@icp.ac.ru

b A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Moscow, Russian Federation, ul. Vavilova, 28, Moscow, Russian Federation

c N.N. Semenov Institute of Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation, ul. Kosygina, 4, 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.

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Article information

DOI
https://doi.org/10.1070/MC2002v012n05ABEH001657
Article type
Paper
Submitted
19 Aug 2002

Mendeleev Commun., 2002,12, 193-196

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

I. V. Vystorop, K. A. Lyssenko, V. N. Voznesensky, V. P. Lodygina and R. G. Kostyanovsky, Mendeleev Commun., 2002, 12, 193 DOI: 10.1070/MC2002v012n05ABEH001657

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