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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
I. E. Chikunov, A. N. Kravchenko, P. A. Belyakov, O. V. Lebedev, N. N. Makhova
N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
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.
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
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