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2-Phenyl-3-hydroxyimidazolidin-4-one: the regioselective synthesis, structure and enantiomerically enriched crystallization

Igor Viktorovich Vystorop 1
Igor Viktorovich Vystorop
, 
Konstantin Alexandrovich Lyssenko 2
Konstantin Alexandrovich Lyssenko
, 
Remir Grigorevich Kostyanovsky 3
Remir Grigorevich Kostyanovsky
10.1070/MC2003v013n03ABEH001790
Published 2003-07-11
Communication , Volume 13, Issue 3, 116-118
6
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Vystorop I. V., Lyssenko K. A., Kostyanovsky R. G. 2-Phenyl-3-hydroxyimidazolidin-4-one: the regioselective synthesis, structure and enantiomerically enriched crystallization // Mendeleev Communications. 2003. Vol. 13. No. 3. pp. 116-118.
GOST all authors (up to 50) Copy
Vystorop I. V., Lyssenko K. A., Kostyanovsky R. G. 2-Phenyl-3-hydroxyimidazolidin-4-one: the regioselective synthesis, structure and enantiomerically enriched crystallization // Mendeleev Communications. 2003. Vol. 13. No. 3. pp. 116-118.
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TY - JOUR
DO - 10.1070/MC2003v013n03ABEH001790
UR - https://mendcomm.colab.ws/publications/10.1070/MC2003v013n03ABEH001790
TI - 2-Phenyl-3-hydroxyimidazolidin-4-one: the regioselective synthesis, structure and enantiomerically enriched crystallization
T2 - Mendeleev Communications
AU - Vystorop, Igor Viktorovich
AU - Lyssenko, Konstantin Alexandrovich
AU - Kostyanovsky, Remir Grigorevich
PY - 2003
DA - 2003/07/11
PB - Mendeleev Communications
SP - 116-118
IS - 3
VL - 13
ER -
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@article{2003_Vystorop,
author = {Igor Viktorovich Vystorop and Konstantin Alexandrovich Lyssenko and Remir Grigorevich Kostyanovsky},
title = {2-Phenyl-3-hydroxyimidazolidin-4-one: the regioselective synthesis, structure and enantiomerically enriched crystallization},
journal = {Mendeleev Communications},
year = {2003},
volume = {13},
publisher = {Mendeleev Communications},
month = {Jul},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2003v013n03ABEH001790},
number = {3},
pages = {116--118},
doi = {10.1070/MC2003v013n03ABEH001790}
}
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Vystorop, Igor Viktorovich, et al. “2-Phenyl-3-hydroxyimidazolidin-4-one: the regioselective synthesis, structure and enantiomerically enriched crystallization.” Mendeleev Communications, vol. 13, no. 3, Jul. 2003, pp. 116-118. https://mendcomm.colab.ws/publications/10.1070/MC2003v013n03ABEH001790.

Abstract

The reaction of glycine hydroxamic acid with benzaldehyde regioselectively affords the title racemic cyclic hydroxamic acid, which crystallises as enantiomorphic crystals (space group P212121) from a methanol solution.

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