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This article is cited in 9 scientific papers (total in 9 papers)
General regioselective synthesis of 2,2-disubstituted 3-hydroxyimidazolidin-4-ones
I. V. Vystoropa, K. A. Lyssenkob, V. N. Voznesenskyc, V. P. Lodyginaa, 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 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.
Citation:
I. V. Vystorop, K. A. Lyssenko, V. N. Voznesensky, V. P. Lodygina, R. G. Kostyanovsky, “General regioselective synthesis of 2,2-disubstituted 3-hydroxyimidazolidin-4-ones”, Mendeleev Commun., 12:5 (2002), 193–196
Linking options:
https://www.mathnet.ru/eng/mendc4157 https://www.mathnet.ru/eng/mendc/v12/i5/p193
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