Highly diastereoselective synthesis of 2-monosubstituted 1R,5S(1S,5R)-glycoluriles on the basis of S- and R-N-carbamoyl-α-amino acids
Konstantin Chegaev
1
,
Pavel A Belyakov
1
,
Elena Yu. Maksareva
1
,
Oleg Lebedev
1
,
Nina N. Makhova
1
Publication type: Journal Article
Publication date: 2003-01-01
scimago Q3
wos Q3
SJR: 0.305
CiteScore: 3.0
Impact factor: 1.7
ISSN: 09599436, 1364551X
General Chemistry
Abstract
The reactions of 4,5-dihydroxyimidazolidin-2-one with chiral S- and R-N-carbamoyl-α-amino acids occur diastereoselectively with the formation of corresponding 1R,5S(1S,5R)-glycoluriles as predominant diastereomers; the absolute configuration is determined for three stereoisomers by X-ray diffraction analysis.
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Total citations:
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Citations from 2025:
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Kravchenko A. N. et al. Highly diastereoselective synthesis of 2-monosubstituted 1R,5S(1S,5R)-glycoluriles on the basis of S- and R-N-carbamoyl-α-amino acids // Mendeleev Communications. 2003. Vol. 13. No. 6. pp. 269-271.
GOST all authors (up to 50)
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Kravchenko A. N., Chegaev K., Chikunov I. E., Belyakov P. A., Maksareva E. Y., Lyssenko K. A., Lebedev O., Makhova N. N. Highly diastereoselective synthesis of 2-monosubstituted 1R,5S(1S,5R)-glycoluriles on the basis of S- and R-N-carbamoyl-α-amino acids // Mendeleev Communications. 2003. Vol. 13. No. 6. pp. 269-271.
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RIS
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TY - JOUR
DO - 10.1070/MC2003v013n06ABEH001802
UR - https://linkinghub.elsevier.com/retrieve/pii/S0959943603705574
TI - Highly diastereoselective synthesis of 2-monosubstituted 1R,5S(1S,5R)-glycoluriles on the basis of S- and R-N-carbamoyl-α-amino acids
T2 - Mendeleev Communications
AU - Kravchenko, Angelina N.
AU - Chegaev, Konstantin
AU - Chikunov, Il’ya E.
AU - Belyakov, Pavel A
AU - Maksareva, Elena Yu.
AU - Lyssenko, Konstantin A.
AU - Lebedev, Oleg
AU - Makhova, Nina N.
PY - 2003
DA - 2003/01/01
PB - OOO Zhurnal "Mendeleevskie Soobshcheniya"
SP - 269-271
IS - 6
VL - 13
SN - 0959-9436
SN - 1364-551X
ER -
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BibTex (up to 50 authors)
Copy
@article{2003_Kravchenko,
author = {Angelina N. Kravchenko and Konstantin Chegaev and Il’ya E. Chikunov and Pavel A Belyakov and Elena Yu. Maksareva and Konstantin A. Lyssenko and Oleg Lebedev and Nina N. Makhova},
title = {Highly diastereoselective synthesis of 2-monosubstituted 1R,5S(1S,5R)-glycoluriles on the basis of S- and R-N-carbamoyl-α-amino acids},
journal = {Mendeleev Communications},
year = {2003},
volume = {13},
publisher = {OOO Zhurnal "Mendeleevskie Soobshcheniya"},
month = {jan},
url = {https://linkinghub.elsevier.com/retrieve/pii/S0959943603705574},
number = {6},
pages = {269--271},
doi = {10.1070/MC2003v013n06ABEH001802}
}
Cite this
MLA
Copy
Kravchenko, Angelina N., et al. “Highly diastereoselective synthesis of 2-monosubstituted 1R,5S(1S,5R)-glycoluriles on the basis of S- and R-N-carbamoyl-α-amino acids.” Mendeleev Communications, vol. 13, no. 6, Jan. 2003, pp. 269-271. https://linkinghub.elsevier.com/retrieve/pii/S0959943603705574.