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

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Denis A. Lenev, Konstantin A. Lyssenko, Remir G. Kostyanovsky, “The chiral drug Albicar: resolution of its racemate via complexation with BINOL”, New J. Chem., 34:3 (2010), 403
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