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  1. Trithiacrown ethers incorporating tetrahydropyridine subunit: synthesis, in vitro and in silico studies of inhibitory activity against α-glucosidase

    Mendeleev Commun., 35:4 (2025),  447–449
  2. New pyridine dithiaazacrown ether derivatives: synthesis, structural characterization, in silico and in vitro biological studies

    Mendeleev Commun., 34:4 (2024),  514–517
  3. 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
  4. Unexpected hydrazine- and hydroxylamine-induced transformations of aza-14-crown-4 incorporating 4-oxopiperidine-3-carboxylate moiety

    Mendeleev Commun., 33:5 (2023),  708–710
  5. Synthesis and biological evaluation of novel phane-structured diazacrowns containing γ-piperidone and pyridine rings

    Mendeleev Commun., 30:6 (2020),  753–755
  6. Unexpected formation of dinaphthoaza-17-crown-5 ether containing γ-aminopiperidine subunit

    Mendeleev Commun., 29:6 (2019),  698–699
  7. Synthesis and cytotoxicity of novel γ-piperidone-containing dibenzo-1,7-diaza-14-crown-4 ethers

    Mendeleev Commun., 29:4 (2019),  375–377
  8. Synthesis and biological activity of (γ-arylpyridino)-dibenzoaza-14-crown-4 ethers

    Mendeleev Commun., 25:3 (2015),  224–225
  9. New hybrids between triterpenoid acids and nucleoside HIV-RT inhibitors

    Mendeleev Commun., 25:2 (2015),  96–98
  10. Synthesis of dibenzopiperidinoaza-14-crown-4 ethers and their one-step conversion into dibenzo-16-crown-3

    Mendeleev Commun., 16:1 (2006),  35–36


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