N. G. Luk'yanenko
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Featured researches published by N. G. Luk'yanenko.
ChemInform | 1983
A. V. Bogatskii; N. G. Luk'yanenko; T. I. Kirichenko
Literature data on methods for the synthesis of cyclic thioureas and their physicochemical properties and transformations are correlated.
Polymer Bulletin | 1989
B. Valter; Václav Janout; Hana Hrudková; Pavel Čefelín; N. G. Luk'yanenko; S. S. Basok; E. Yu. Kulygina
SummaryImmobilized aza-15-crown-5 were prepared by the reaction of chloromethylated polystyrene resin with N-(2-hydroxyethyl)-aza-15-crown-5. These polymer-supported crowns were very effective catalysts of nucleophilic substitution reactions carried out under the conditions of the two-phase (L-S) or three-phase (L-S-L) catalysis.
Chemistry of Heterocyclic Compounds | 1987
N. G. Luk'yanenko; V. N. Pastushok; L. E. Tonya; R. G. Kostyanovskii
The synthesis of some novel benzo-crown ethers by α-amidomethylation is described.
Chemistry of Heterocyclic Compounds | 1987
N. G. Luk'yanenko; T. A. Kirichenko; V. V. Limich; A. V. Bogatskiit
The reaction of polyoxyethylene diamines with polyoxyethylene diisothiocyanates leads to new crowns with thiocarbamide groups having 13- to 34-membered rings. Binuclear crown compounds with thiocarbamide groups are prepared by the reaction of polyoxyethylene diisothiocyanates with aza-15-crown-5.
Chemistry of Heterocyclic Compounds | 1987
V. Ganin; V. F. Makarov; N. G. Luk'yanenko; S. A. Kotlyar
Acylated aza crown ethers containing fragments of N-substituted phthalamic acids in the side chain were obtained by the reaction of monoaza-15-crown-5, monoaza-18-crown-6, and diaza-18-crown-6 with N-substituted isophthalimides.
Pharmaceutical Chemistry Journal | 1988
T. A. Voronina; T. L. Karaseva; N. Ya. Golovenko; M. G. Rokachinskaya; S. S. Basok; S. E. Sharapova; E. Yu. Kulygina; N. G. Luk'yanenko
i. A. B. Nikonova, N. V. Makarova, and S. A. Titov, Zh. Vyssh. Nervn. Deyat., 37, No. 3, 570-572 (1987). 2. S. A. Titov, O. G. Voskresenskaya, I. Yu. Shamakina, and I. P. Ashmarin, Dokl. Akad. Nauk SSSR, 264, Na. 5, 1269-1272 (1982). 3.
Chemistry of Heterocyclic Compounds | 1988
A. I. Gren; N. G. Luk'yanenko; A. V. Mazepa; O. T. Mel'nik; O. S. Timofeev
. A. Titov, I. Yu. Shamakina, and I. P. Ashmarin, Byull. Eksp. Biol., 45, No. 2, 31-33 (1983).
Chemistry of Heterocyclic Compounds | 1987
N. G. Luk'yanenko; A. V. Lobach; M. N. Parfenova; L. N. Lyamtseva; O. S. Timofeev; A. I. Gren
. I.~Yu. Shamakina, S. A. Titov, A. B. Nikonova, and O. G. Voskresenskaya, Zh. Vyssh. Nervn. Deyat., 37, No. i, 100-105 (1987). 5. J. P. H. Burbach and J. L. M. Leboille, J. Biol. Chem., 258, No. 3, 1487-1494 (1983). 6. J. P. H. Burbach, G. L. Kovacs, D. de Wied, et al., Science, 221, No. 4617, 1310-1312 (1983).
Chemistry of Heterocyclic Compounds | 1987
N. G. Luk'yanenko; O. T. Mel'nik
The mass-spectral analytical characteristics of binuclear crown ethers were established. The determining role of 1,5- and 1,4-C-H...O transannular interactions in the realization of rearrangement processes during fragmentation were ascertained.
Chemistry of Heterocyclic Compounds | 1986
A. V. Bogatskii; E. V. Ganin; V. F. Makarov; S. A. Kotlyar; N. G. Luk'yanenko
The corresponding bis(crown ethers), as well as phenyl- and hydroxy-substituted crown ethers, were obtained by homolytic dehydrodimerization of 12-crown-4, 15-crown-5, and 18-crown-6 in benzene or water.