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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2001 Volume 11, Issue 4, Pages 134–136 (Mi mendc4257)

This article is cited in 37 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.

Language: English

DOI: 10.1070/MC2001v011n04ABEH001469



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