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Mendeleev Communications, 2001, Volume 11, Issue 4, Pages 134–136
DOI: https://doi.org/10.1070/MC2001v011n04ABEH001469
(Mi mendc4257)
 

This article is cited in 39 scientific papers (total in 39 papers)

Crystal properties of N-alkyl-substituted glycolurils as the precursors of chiral drugs

R. G. Kostyanovskya, K. A. Lyssenkob, A. N. Kravchenkoc, O. V. Lebedevc, G. K. Kadorkinaa, V. R. Kostyanovskya

a N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation
b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
c N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: 2,6-Dimethylglycoluril 1 crystallises to form a conglomerate (space group P21) and co-crystallises with isomeric 2,8-dimethylglycoluril 2; 2,6-diethylglycoluril A is the best precursor in the synthesis of chiral drugs.
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Document Type: Article
Language: English


Citation: R. G. Kostyanovsky, K. A. Lyssenko, A. N. Kravchenko, O. V. Lebedev, G. K. Kadorkina, V. R. Kostyanovsky, “Crystal properties of N-alkyl-substituted glycolurils as the precursors of chiral drugs”, Mendeleev Commun., 11:4 (2001), 134–136
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  • https://www.mathnet.ru/eng/mendc/v11/i4/p134
  • This publication is cited in the following 39 articles:
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