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General regioselective synthesis of 2,2-disubstituted 3-hydroxyimidazolidin-4-ones

Igor Viktorovich Vystorop 1
Igor Viktorovich Vystorop
, 
Konstantin Alexandrovich Lyssenko 2
Konstantin Alexandrovich Lyssenko
, 
Vladimir N Voznesensky 3
Vladimir N Voznesensky
, 
Vera Petrovna Lodygina 1
Vera Petrovna Lodygina
, 
Remir Grigorevich Kostyanovsky 3
Remir Grigorevich Kostyanovsky
10.1070/MC2002v012n05ABEH001657
Published 2002-11-15
Communication , Volume 12, Issue 5, 193-196
9
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Vystorop I. V. et al. General regioselective synthesis of 2,2-disubstituted 3-hydroxyimidazolidin-4-ones // Mendeleev Communications. 2002. Vol. 12. No. 5. pp. 193-196.
GOST all authors (up to 50) Copy
Vystorop I. V., Lyssenko K. A., Voznesensky V. N., Lodygina V. P., Kostyanovsky R. G. General regioselective synthesis of 2,2-disubstituted 3-hydroxyimidazolidin-4-ones // Mendeleev Communications. 2002. Vol. 12. No. 5. pp. 193-196.
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TY - JOUR
DO - 10.1070/MC2002v012n05ABEH001657
UR - https://mendcomm.colab.ws/publications/10.1070/MC2002v012n05ABEH001657
TI - General regioselective synthesis of 2,2-disubstituted 3-hydroxyimidazolidin-4-ones
T2 - Mendeleev Communications
AU - Vystorop, Igor Viktorovich
AU - Lyssenko, Konstantin Alexandrovich
AU - Voznesensky, Vladimir N
AU - Lodygina, Vera Petrovna
AU - Kostyanovsky, Remir Grigorevich
PY - 2002
DA - 2002/11/15
PB - Mendeleev Communications
SP - 193-196
IS - 5
VL - 12
ER -
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@article{2002_Vystorop,
author = {Igor Viktorovich Vystorop and Konstantin Alexandrovich Lyssenko and Vladimir N Voznesensky and Vera Petrovna Lodygina and Remir Grigorevich Kostyanovsky},
title = {General regioselective synthesis of 2,2-disubstituted 3-hydroxyimidazolidin-4-ones},
journal = {Mendeleev Communications},
year = {2002},
volume = {12},
publisher = {Mendeleev Communications},
month = {Nov},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2002v012n05ABEH001657},
number = {5},
pages = {193--196},
doi = {10.1070/MC2002v012n05ABEH001657}
}
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Vystorop, Igor Viktorovich, et al. “General regioselective synthesis of 2,2-disubstituted 3-hydroxyimidazolidin-4-ones.” Mendeleev Communications, vol. 12, no. 5, Nov. 2002, pp. 193-196. https://mendcomm.colab.ws/publications/10.1070/MC2002v012n05ABEH001657.

Abstract

The reactions of glycine hydroxamic acid with aliphatic ketones and acetophenone are commonly used for the regioselective synthesis of cyclic hydroxamic acids 6a–e; spiro hydroxamic acid 6a was structurally characterised by X-ray diffraction analysis.

References

1.
Photochemistry of hydroxamic acids and derivatives
Lipczynska-Kochany E.
Chemical Reviews, 1991
2.
Hydroxamic and aminohydroxamic acids and their complexes with metal ions
Kurzak B., Kozłowski H., Farkas E.
Coordination Chemistry Reviews, 1992
4.
Design and Therapeutic Application of Matrix Metalloproteinase Inhibitors
Whittaker M., Floyd C.D., Brown P., Gearing A.J.
Chemical Reviews, 1999
5.
Therapeutic Potential and Strategies for Inhibiting Tumor Necrosis Factor-α
Newton R.C., Decicco C.P.
Journal of Medicinal Chemistry, 1999
8.
A cyclohexane-1,2-diyldinitrilotetraacetate tetrahydroxamate derivative for actinide complexation: synthesis and complexation studies
Santos M.A., Rodrigues E., Gaspar M.
Journal of the Chemical Society Dalton Transactions, 2000
10.
10.1070/MC2002v012n05ABEH001657_bib5
Vystorop
Izv. Akad. Nauk, Ser. Khim., 2000
11.
10.1070/MC2002v012n05ABEH001657_bib6
Charbonnel
Compt. Rend., 1966
13.
10.1070/MC2002v012n05ABEH001657_bib8
Challis
1978
14.
10.1070/MC2002v012n05ABEH001657_bib9_1
Grigor’ev
Izv. Akad. Nauk, Ser. Khim., 2000
15.
10.1070/MC2002v012n05ABEH001657_bib9_2
Shchukin
Khim. Geterotsikl. Soedin., 1990
16.
Crystal and molecular structure of glycinehydroxamic acid
Głowiak T., Koralewicz M.
Journal of Chemical Crystallography, 1985
17.
10.1070/MC2002v012n05ABEH001657_bib11_1
Allen
J. Chem. Soc., Perkin Trans., 1987
18.
Bond Angles in Lactones and Lactams
Nørskov-Lauritsen L., Bürgi H., Hofmann P., Schmidt H.R.
Helvetica Chimica Acta, 1985
19.
Karlíček R., Polášek M.
Collection of Czechoslovak Chemical Communications, 2010
21.
Structure and mechanism in complex general acid-base catalyzed reactions
Jencks W.P., Sayer J.M.
Faraday Symposia of the Chemical Society, 1975
23.
Condensation of aldehydes and ketones with dipeptides
Panetta C.A., Pesh-Imam M.
Journal of Organic Chemistry, 1972
24.
10.1070/MC2002v012n05ABEH001657_bib15
Chan
Angew. Chem., Int. Ed. Engl., 1966
26.
10.1070/MC2002v012n05ABEH001657_bib16_2
Wolfe
J. Chem. Soc. (B), 1971
27.
A New Efficient Synthesis of (R,R)-2,2′-Bipyrrolidine: An Interesting Chiral 1,2-Diamine withC2 Symmetry
Alexakis A., Tomassini A., Chouillet C., Roland S., Mangeney P., Bernardinelli G.
Angewandte Chemie - International Edition, 2000
29.
10.1070/MC2002v012n05ABEH001657_bib19
Ouannes
Bull. Soc. Chim. Fr., 1965
30.
Hydrogen-bond geometry in organic crystals
Taylor R., Kennard O.
Accounts of Chemical Research, 1984
31.
449. Hydroxamic acids. Part II. The synthesis and structure of cyclic hydroxamic acids from pyridine and quinoline
Cunningham K.G., Newbold G.T., Spring F.S., Stark J.
Journal of the Chemical Society (Resumed), 1949