I. E. Chikunov, A. N. Kravchenko, P. A. Belyakov, K. A. Lyssenko, V. V. Baranov, O. V. Lebedev, N. N. Makhova, “Synthesis of 1S,5R- and 1R,5S-glycoluriles by diastereospecific α-ureidoalkylation of (S)/(R)-N-carbamoyl-α-amino acids with 4,5-dihydroxyimidazolidin-2-one”, Mendeleev Commun., 14:6 (2004), 253

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Mendeleev Communications, 2004, Volume 14, Issue 6, Pages 253–255
DOI: https://doi.org/10.1070/MC2004v014n06ABEH002050 (Mi mendc3900)

This article is cited in 15 scientific papers (total in 15 papers)

Synthesis of 1S,5R- and 1R,5S-glycoluriles by diastereospecific α-ureidoalkylation of (S)/(R)-N-carbamoyl-α-amino acids with 4,5-dihydroxyimidazolidin-2-one

I. E. Chikunov^a, A. N. Kravchenko^a, P. A. Belyakov^a, K. A. Lyssenko^b, V. V. Baranov^a, O. V. Lebedev^a, N. N. Makhova^a

^a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
^b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation

Full-text PDF (319 kB) Citations (15)

DOI: https://doi.org/10.1070/MC2004v014n06ABEH002050

Abstract: A diastereospecific method for the synthesis of individual enantiomers of 1S,5R- and 1R,5S-glycoluriles has been developed based on the α-ureidoalkylation of (S)/(R)-N-carbamoyl-α-amino acids with 4,5-dihydroxyimidazolidin-2-one.

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Document Type: Article

Language: English

Citation: I. E. Chikunov, A. N. Kravchenko, P. A. Belyakov, K. A. Lyssenko, V. V. Baranov, O. V. Lebedev, N. N. Makhova, “Synthesis of 1S,5R- and 1R,5S-glycoluriles by diastereospecific α-ureidoalkylation of (S)/(R)-N-carbamoyl-α-amino acids with 4,5-dihydroxyimidazolidin-2-one”, Mendeleev Commun., 14:6 (2004), 253–255

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This publication is cited in the following 15 articles:

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