Issue 6, 2004
From the journal:

Mendeleev Communications

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

Il'ya E. Chikunov,a   Angelina N. Kravchenko,a   Pavel A. Belyakov,a   Konstantin A. Lyssenko,b   Vladimir V. Baranov,a   Oleg V. Lebedeva  and  Nina N. Makhovaa  

a N.D.Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation, Leninsky prospekt, 47, Moscow, Russian Federation

b A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Moscow, Russian Federation, ul. Vavilova, 28, Moscow, Russian Federation

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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Article information

DOI
https://doi.org/10.1070/MC2004v014n06ABEH002050
Article type
Communication
Submitted
29 Sep 2004

Mendeleev Commun., 2004,14, 253-255

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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. N. Kravchenko, P. A. Belyakov, K. A. Lyssenko, V. V. Baranov, O. V. Lebedev and N. N. Makhova, Mendeleev Commun., 2004, 14, 253 DOI: 10.1070/MC2004v014n06ABEH002050

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