Issue 3, 2002
From the journal:

Mendeleev Communications

3-Hydroxy-2,2-dimethylimidazolidin-4-one: the regioselective synthesis and chiral crystallization

Igor V. Vystorop,   Konstantin A. Lyssenko  and  Remir G. Kostyanovsky  

Abstract

The condensation of glycine hydroxamic acid with acetone regioselectively leads to the formation of the title achiral cyclic hydroxamic acid, which crystallises from an acetone solution as chiral crystals (space groupP2 1 2 1 2 1 ) of (P,1R,3S) and (M,1S,3R) enantiomers.

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Article information

DOI
https://doi.org/10.1070/MC2002v012n03ABEH001603
Article type
Paper

Mendeleev Commun., 2002,12, 85-87

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3-Hydroxy-2,2-dimethylimidazolidin-4-one: the regioselective synthesis and chiral crystallization

I. V. Vystorop, K. A. Lyssenko and R. G. Kostyanovsky, Mendeleev Commun., 2002, 12, 85 DOI: 10.1070/MC2002v012n03ABEH001603

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