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Nenajdenko Valentin Georgievich

Publications in Math-Net.Ru

  1. First synthesis of 1,10-phenanthroline-2,9-diamine dioxides, a novel family of phenanthroline-based ligands

    Mendeleev Commun., 35:6 (2025),  720–722
  2. Piperidine- and 2-(p-tolyl)piperidine-derived DAPhen ligands: the aryl substituent unexpectedly suppresses the extraction efficiency

    Mendeleev Commun., 35:5 (2025),  540–542
  3. Lanthanide complexes with (4,7-dichloro-1,10-phenanthroline-2,9-diyl)bis(pyrrolidin-1-ylmethanone): bifunctional materials for homogeneous catalysis and luminescent thermometry

    Mendeleev Commun., 34:6 (2024),  825–827
  4. The chemistry of heterocycles in the 21st century

    Usp. Khim., 93:7 (2024),  1–366
  5. First examples of 1,1-diazido-2-sulfonylalkenes

    Mendeleev Commun., 33:6 (2023),  756–758
  6. Stereoselective epoxidation of 4-fluoro-4-nitrocyclohexenes

    Mendeleev Commun., 33:4 (2023),  463–465
  7. The first example of fluoro-Meinwald rearrangement

    Mendeleev Commun., 33:2 (2023),  188–190
  8. The green chemistry paradigm in modern organic synthesis

    Usp. Khim., 92:12 (2023),  1–187
  9. Di- and polyazides. Synthesis, chemical transformations and practical applications

    Usp. Khim., 92:1 (2023),  1–49
  10. Copper-containing polymethylsilsesquioxane nanocomposites in catalytic olefination reaction

    Mendeleev Commun., 32:4 (2022),  478–481
  11. Diene-transmissive hetero-Diels–Alder reaction of distyryl thioketone

    Mendeleev Commun., 32:3 (2022),  384–385
  12. [3,3]-Sigmatropic rearrangements: a variety of methods and recent advances

    Usp. Khim., 91:8 (2022),  1–95
  13. Significant impact of lanthanide contraction on the structure of the phenanthroline complexes

    Mendeleev Commun., 31:6 (2021),  853–855
  14. Arylhydrazones of α-keto esters via methanolysis of dichlorodiazabutadienes: synthesis and structural study

    Mendeleev Commun., 31:5 (2021),  677–679
  15. Supramolecular organic frameworks derived from bromoaryl-substituted dichlorodiazabutadienes via Cl···Br halogen bonding

    Mendeleev Commun., 31:2 (2021),  191–193
  16. New family of polydentate tetrazole-pyrazoline ligands prepared by the azido-Ugi reaction

    Mendeleev Commun., 31:1 (2021),  48–50
  17. Hydrogen bonding in acetylene containing dichlorodiazaalkadienes

    Mendeleev Commun., 30:5 (2020),  615–617
  18. Trifluoroacetyl substituted pyrazolotriazines: synthesis and pathways of formation

    Mendeleev Commun., 30:2 (2020),  180–182
  19. Access to molecular complexity. Multicomponent reactions involving five or more components

    Usp. Khim., 89:11 (2020),  1274–1336
  20. Recent advances in the chemistry of pyridazine — an important representative of six-membered nitrogen heterocycles

    Usp. Khim., 89:4 (2020),  393–429
  21. PASE synthesis of 1-azolyl-1H-1,2,4-triazoles by the reaction of diazoazoles with ethyl isocyanoacetate

    Mendeleev Commun., 29:6 (2019),  653–654
  22. Reaction of 3-azidoisoxazoles with active methylene compounds

    Mendeleev Commun., 29:5 (2019),  529–530
  23. Diastereoselective vinylogous Mannich reaction of perfluoroalkylated cyclic imines with 2-trimethylsilyloxyfuran

    Mendeleev Commun., 29:1 (2019),  57–58
  24. Organofluorine chemistry: promising growth areas and challenges

    Usp. Khim., 88:5 (2019),  425–569
  25. Diazocarbonyl derivatives of amino acids: unique chiral building blocks for the synthesis of biologically active compounds

    Usp. Khim., 88:3 (2019),  248–279
  26. Synthesis of chiral α-(tetrazol-1-yl)-substituted carboxylic acids

    Mendeleev Commun., 28:4 (2018),  364–365
  27. Synthesis of azacycloalkane-1,2-fused pyrroles via alkylation of cyclic ketimines with α-bromo ketones

    Mendeleev Commun., 28:3 (2018),  270–271
  28. Aza-Henry reaction with trifluoropiruvate ketimines

    Mendeleev Commun., 28:2 (2018),  133–134
  29. Aza-Henry reaction with perfluoroalkylated cyclic ketimines

    Mendeleev Commun., 28:1 (2018),  81–82
  30. Reaction of CF3-ynones with azides. An efficient regioselective and metal-free route to 4-trifluoroacetyl-1,2,3-triazoles

    Mendeleev Commun., 28:1 (2018),  17–19
  31. Acetylene–azide click macrocyclization of peptides

    Usp. Khim., 87:7 (2018),  619–635
  32. $^{18}\mathrm{F}$-Labelled catecholamine type radiopharmaceuticals in the diagnosis of neurodegenerative diseases and neuroendocrine tumours: approaches to synthesis and development prospects

    Usp. Khim., 87:4 (2018),  350–373
  33. Cyanothioacetamide: a polyfunctional reagent with broad synthetic utility

    Usp. Khim., 87:1 (2018),  1–27
  34. Copper catalyzed alkyne–azide cycloaddition with 3-propargyl- γ-butyrolactones

    Mendeleev Commun., 27:6 (2017),  562–564
  35. Transformation of cyclic ketimines to oxaziridines and nitrones

    Mendeleev Commun., 27:1 (2017),  29–30
  36. Oxidative Nef reaction of trifluoromethylated 2-nitroalkanamines

    Mendeleev Commun., 26:6 (2016),  511–512
  37. Efficient synthesis of triazole-containing spiro dilactones

    Mendeleev Commun., 26:1 (2016),  11–13
  38. Synthesis of 1,1,1-trifluorobut-3-yn-2-ones and their reactions with N-nucleophiles

    Mendeleev Commun., 24:6 (2014),  342–344
  39. Computational study of the catalytic olefination reaction

    Mendeleev Commun., 24:6 (2014),  340–341
  40. Synthesis of trifluoromethylated [1,4]diazepines from 1,1,1-trifluoroalk-3-yn-2-ones

    Mendeleev Commun., 24:5 (2014),  269–271
  41. Development of new methods in modern selective organic synthesis: preparation of functionalized molecules with atomic precision

    Usp. Khim., 83:10 (2014),  885–985
  42. Betulonic acid–peptide conjugates: synthesis and evaluation of anti-inflammatory activity

    Mendeleev Commun., 23:5 (2013),  260–261
  43. Friedel–Crafts alkylation of natural amino acid-derived pyrroles with CF3-substituted cyclic imines

    Mendeleev Commun., 23:2 (2013),  92–93
  44. R-α-Phenylglycinol and R-α-phenylglycinamide as novel chiral templates in diastereoselective Ugi reaction

    Mendeleev Commun., 21:5 (2011),  245–246
  45. Cu and Au nanocomposites in catalytic olefination reaction

    Mendeleev Commun., 20:4 (2010),  200–202
  46. α-Acyl lactams in the synthesis of physiologically active compounds

    Usp. Khim., 78:5 (2009),  466–493
  47. A new synthesis of substituted 2-trifluoromethylindoles

    Mendeleev Commun., 18:6 (2008),  327–328
  48. From thiophene to Sulflower

    Mendeleev Commun., 18:4 (2008),  171–179
  49. Baylis–Hilman reaction for α,β-unsaturated trifluoromethyl ketones

    Mendeleev Commun., 16:5 (2006),  273–274
  50. EWG-containing thiophene- and 2-thiolene-1,1-dioxides as promising electrophiles for organic synthesis

    Mendeleev Commun., 16:4 (2006),  215–218
  51. Mild and regioselective straightforward synthesis of isomelatonin analogues

    Mendeleev Commun., 16:4 (2006),  213–215
  52. Diastereoselective synthesis of α-hydroxydihydropyrans containing the CF3 group

    Mendeleev Commun., 16:3 (2006),  180–182
  53. Stereoselective synthesis of 1-bromo-1-fluorostyrenes

    Mendeleev Commun., 16:3 (2006),  179–180
  54. α-Pentafluoroethylated amines: a new synthetic approach

    Mendeleev Commun., 16:3 (2006),  141–143
  55. Thiophene 1,1-dioxides as unique building blocks in modern organic synthesis and materials chemistry

    Usp. Khim., 75:12 (2006),  1139–1174
  56. Olefination of carbonyl compounds: modern and classical methods

    Usp. Khim., 73:10 (2004),  1039–1074
  57. Methods for the synthesis of α,β-unsaturated trifluoromethyl ketones and their use in organic synthesis

    Usp. Khim., 68:6 (1999),  483–505


© Steklov Math. Inst. of RAS, 2026