D. T. Nguyen, N. T. Dao, V. T. T. Tran, T. Q. Le, L. M. Nguyen, A. T. Le, “Trithiacrown ethers incorporating tetrahydropyridine subunit: synthesis, <em>in vitro</em> and <em>in silico</em> studies of inhibitory activity against α-glucosidase”, Mendeleev Commun., 35:4 (2025), 447–449
2024
2.
V. T. T. Tran, N. T. Dao, T. T. Do, T. T. T. Pham, D. T. Le, V. N. Khrustalev, Ph. T. T. Nguyen, A. T. Le, “New pyridine dithiaazacrown ether derivatives: synthesis, structural characterization, in silico and in vitro biological studies”, Mendeleev Commun., 34:4 (2024), 514–517
N. T. Dao, T. T. Do, T. T. T. Pham, V. T. T. Tran, V. N. Khrustalev, A. T. Le, “Molecular structure and ultrasound-assisted synthesis of the diazacrown derivative containing 2,3,4,6-tetraaryl-γ piperidone”, Mendeleev Commun., 33:5 (2023), 711–713
D. T. T. Nguyen, H. H. Truong, N. T. Dao, V. T. T. Tran, O. S. Gorchakova, A. T. Le, “Unexpected hydrazine- and hydroxylamine-induced transformations of aza-14-crown-4 incorporating 4-oxopiperidine-3-carboxylate moiety”, Mendeleev Commun., 33:5 (2023), 708–710
L. M. Nguyen, H. H. Truong, V. N. Khrustalev, S. T. Truong, D. T. Nguyen, V. T. Tran, S. T. Mai, V. T. Tran, A. T. Le, “Synthesis and biological evaluation of novel phane-structured diazacrowns containing γ-piperidone and pyridine rings”, Mendeleev Commun., 30:6 (2020), 753–755
A. T. Le, V. T. Tran, H. H. Truong, L. M. Nguyen, D. M. Luong, T. T. Do, D. T. Nguyen, N. T. Dao, D. T. Le, A. T. Soldatenkov, V. N. Khrustalev, “Synthesis and cytotoxicity of novel γ-piperidone-containing dibenzo-1,7-diaza-14-crown-4 ethers”, Mendeleev Commun., 29:4 (2019), 375–377
