This article is cited in 2 scientific papers (total in 2 papers)
Synthesis of (S)-N-hydantoinoalkylglycoluriles by one-pot double cyclisation of chiral α,ω-diureido acids under the action of 4,5-dihydroxyimidazolidin-2-ones
Abstract:
The reaction of 4,5-dihydroxyimidazolidin-2-ones with chiral (S)-N,N’-dicarbamoyl-α,ω-amino acids occurs as one-pot double cyclisation under acid catalysis to give the corresponding glycoluriles with (S)-N-hydantoinoalkyl substituents.
Document Type:
Article
Language: English
Citation:
I. E. Chikunov, A. N. Kravchenko, P. A. Belyakov, O. V. Lebedev, N. N. Makhova, “Synthesis of (S)-N-hydantoinoalkylglycoluriles by one-pot double cyclisation of chiral α,ω-diureido acids under the action of 4,5-dihydroxyimidazolidin-2-ones”, Mendeleev Commun., 15:2 (2005), 67–69
Linking options:
https://www.mathnet.ru/eng/mendc3679
https://www.mathnet.ru/eng/mendc/v15/i2/p67
This publication is cited in the following 2 articles:
A. N. Kravchenko, E. Yu. Maksareva, S. V. Vasilevskii, O. V. Lebedev, K. A. Lyssenko, “A new approach to the synthesis of 1,3-dimethyl-4,5-disubstituted imidazolidin-2-ones”, Mendeleev Commun., 18:1 (2008), 45–47
Il'ya E. Chikunov, Angelina N. Kravchenko, Pavel A. Belyakov, Oleg V. Lebedev, Nina N. Makhova, “Synthesis of (S)‐N‐Hydantoinoalkylglycoluriles by One‐Pot Double Cyclization of Chiral α,ω‐Diureido Acids under the Action of 4,5‐Dihydroxyimidazolidin‐2‐ones.”, ChemInform, 36:36 (2005)
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