Abstract:
A qualitative conception for constructing conglomerates has been proposed; bis-lactam 1 has been synthesised by two methods, and it exhibited a priori predicted properties like formation in the optically active form under conditions of a routine crystallization.
Document Type:
Article
Language: English
Citation:
R. G. Kostyanovsky, I. A. Bronzova, K. A. Lyssenko, “Directed synthesis of compounds capable to spontaneous resolution”, Mendeleev Commun., 12:1 (2002), 4–6
Linking options:
https://www.mathnet.ru/eng/mendc4065
https://www.mathnet.ru/eng/mendc/v12/i1/p4
This publication is cited in the following 10 articles:
D. P. Gerasimova, E. Sh. Saigitbatalova, D. R. Islamov, D. V. Zakharychev, A. F. Saifina, A. R. Kurbangalieva, O. A. Lodochnikova, “REPRODUCIBILITY OF A HOMOCHIRAL HYDROGEN-BONDED CHAIN IN CONGLOMERATE AND RACEMIC COMPOUND CRYSTALS OF THE TRIAZOLE DERIVATIVE OF 3-PYRROLINE-2-ONE”, J Struct Chem, 63:9 (2022), 1434
Olga A. Lodochnikova, Aigul R. Zaripova, Robert R. Fayzullin, Aida I. Samigullina, Irina I. Vandyukova, Lubov N. Potapova, Almira R. Kurbangalieva, ““Doubly enantiophobic” behavior during crystallization of racemic 1,5-dihydro-2H-pyrrol-2-one thioether”, CrystEngComm, 20:23 (2018), 3218
O. A. Lodochnikova, Yu. K. Voronina, L. Z. Latypova, D. B. Krivolapov, A. R. Kurbangalieva, I. A. Litvinov, “Crystallization of racemic 4-arylsulfonyl-2(5H)-furanones: reproducibility of homochiral associates, conditions for the spontaneous resolution of enantiomers and the formation of racemic compounds, the role of intermolecular interactions”, Russ Chem Bull, 62:5 (2013), 1218
G. A. Gazieva, P. V. Lozhkin, V. V. Baranov, Yu. V. Nelyubina, A. N. Kravchenko, N. N. Makhova, “4,5-Dihydroxyimidazolidin-2-ones in an α-ureidoalkylation reaction of N-(carboxyalkyl)-, N-(hydroxyalkyl)-, and N-(aminoalkyl)ureas 3. α-Ureidoalkylation of N-[2-(dimethylamino)ethyl]urea”, Russ Chem Bull, 58:12 (2009), 2488
D. A. Lenev, K. A. Lyssenko, R. G. Kostyanovsky, “Crystal engineering strategies in alkane-bis(ammonium) 2,5-diaza-3,6-dioxobicyclo[2.2.2]octane-1,4-dicarboxylates”, Mendeleev Commun., 14:6 (2004), 312–314
Vladimir Yu. Torbeev, Konstantin A. Lyssenko, Oleg N. Kharybin, Mikhail Yu. Antipin, Remir G. Kostyanovsky, “Lamellar Racemic Twinning as an Obstacle for the Resolution of Enantiomers by Crystallization: The Case of Me(All)N+(CH2Ph)Ph X- (X = Br, I) Salts”, J. Phys. Chem. B, 107:48 (2003), 13523
R. G. Kostyanovsky, “Louis Pasteur did it for us especially”, Mendeleev Commun., 13:3 (2003), 85–90
Remir G. Kostyanovsky, Konstantin A. Lyssenko, Denis A. Lenev, Irina A. Bronzova, “Competitive H-bonding in bicyclic bis-lactams: self-assembly in nanotubes or in unbalanced chiral threefold interpenetrated diamondoid network”, Tetrahedron: Asymmetry, 13:24 (2002), 2697
Konstantin A. Lyssenko, Denis A. Lenev, Remir G. Kostyanovsky, “Self-assembly of cage structures. Paper 12: The synthesis and crystal structures of 2,5-diazabicyclo[2.2.2]octane-3,6-dione-1,4-dicarboxylic acids and their diesters”, Tetrahedron, 58:42 (2002), 8525
R. G. Kostyanovsky, G. K. Kadorkina, K. A. Lyssenko, V. Yu. Torbeev, A. N. Kravchenko, O. V. Lebedev, G. V. Grintselev-Knyazev, V. R. Kostyanovsky, “Chiral drugs via the spontaneous resolution”, Mendeleev Commun., 12:1 (2002), 6–8
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