Organic Chemistry

RU

Publications in 2021

  1. Strelnikova J. O., Rostovskii N. V., Khoroshilova O. V., Khlebnikov A. F., Novikov M.S., An Efficient Synthesis of Functionalized 2H-1,3,5-Oxadiazines via Metal-Carbenoid-Induced 1,2,4-Oxadiazole Ring Cleavage. Synthesis 2021, 53, 348–358. DOI: 10.1055/s-0040-1707278.
  2. Kozina D. O., Shakirova J. R., Galenko E. E., Porsev V. V., Gurzhiy V. V., Khlebnikov A. F., Tunik S. P., Unusual Reactivity and Photophysical Properties of Platinum(II) Pincer Complexes Containing 6,6'-Diphenyl-2,2'-bipyridine Ligands. Eur. J. Inorg. Chem. 2021, 117–125. DOI: 10.1055/s-0040-1707278.
  3. Kazakova A. V., Rubicheva L. G., Konev A. S., Khlebnikov, A. F. Stereoselective synthesis of PEGylated azoles via 1,3-dipolar cycloaddition. Tetrahedron 2021, 77, 131774. DOI: 10.1016/j.tet.2020.131774.
  4. Kartsova L. A., Makeeva D. V., Kravchenko A. V., Moskvichev D. O., Polikarpova D.A. Capillary electrophoresis as a powerful tool for the analyses of bacterial samples. TrAC – Trends in Analyt. Chem. 2021, 134, 116110. DOI: 10.1016/j.trac.2020.116110.
  5. Mikhaylov V.N., Kazakov I.V., Parfeniuk T.N., Khoroshilova O.V., Scheer M., Timoshkin A.Y., Balova I.A., The carbene transfer to strong Lewis acids: copper is better than silver. Dalton Trans. 2021, 50, 2872. DOI: 10.1039/d1dt00235j.
  6. Efremova M.M., Govdi A.I., Frolova V.V., Rumyantsev A.M., Balova I.A., Design and synthesis of new 5-aryl-4-arylethynyl-1H-1,2,3-triazoles with valuable photophysical and biological properties. Molecules, 2021, 26, 2801. DOI: 10.3390/molecules26092801.
  7. Bessonova E.A., Kartsova L.A., Moskvichev D.O., Ionic Liquids in Electrophoretic Separation and Preconcentration Processes. J. Analyt. Chem., 2021, 76, 1111. DOI: 10.1134/S1061934821100038.
  8. Kartsova L.A., Solov’eva S.A., Bessonova E.A. Microemulsion Preconcentration of Steroid Hormones from Aqueous Solutions and Urine Samples. J. Analyt. Chem., 2021, 76, 1058. DOI: 10.1134/S1061934821090057.
  9. Kartsova L.A., Somova V.D., Bessonova E.A. Determination of Zoledronic Acid and Creatinine by Hydrophilic Chromatography. J. Analyt Chem., 2021, 76, 221. DOI: 10.1134/S1061934821020106.
  10. Kasatkina S.O., Geyl K.K., Baykov S.V., Boyarskaya, I.A., Boyarskiy, V.P., Org. Biomol. Chem., 2021, 19, 6059. DOI: 10.1039/d1ob00783a.
  11. Zalivatskaya A.S., Golovanov A.A., Boyarskaya I.A., Kruykova M.A., Khoroshilova O.V., Vasilyev A.V., Triflic Acid Promoted Transformations of Linear-Conjugated Enynones and their Reactions with Arenes. Synthesis of Dihydropyranones, Conjugated Dienones, and Indanes. Eur. J. Org. Chem., 2021, 2634. DOI 10.1002/ejoc.202100280.
  12. Zerov A.V., Boyarskaya I.A., Khoroshilova O.V., Lavrentieva I.N., Slita A.V., Sinegubova E.O., Zarubaev V.V., Vasilyev A.V., TfOH-Promoted Reactions of TMS-Ethers of CF3-Pentenynoles with Arenes. Synthesis of CF3-Substituted Pentenynes, Indenes, and Other Carbocyclic Structures. J. Org. Chem., 2021, 86, 1489. DOI 10.1021/acs.joc.0c02361.
  13. Puzanov A.I., Ryabukhin D.S., Zalivatskaya A.S., Zakusilo D.N., Mikson D.S., Boyarskaya I.A., Vasilyev A.V., Synthesis of 5-arylacetylenyl-1,2,4-oxadiazoles and their transformations under superelectrophilic activation conditions. Beilstein J. Org. Chem., 2021, 17, 2417. DOI: 10.3762/bjoc.17.158.
  14. Evstigneyev E.I.,Grinenko E.V.,Mazur A.S.,Vasilyev A.V., Study of the formation of lignin hydrogels with metal cations. J. Wood Chem. Tech., 2021, 41, 73. DOI 10.1080/02773813.2021.1873389.
  15. Galenko E.E.,Bodunov V.A.,Kryukova M.A.,Novikov M.S.,Khlebnikov A.F., Buchner Reaction/Azirine Modification Approach Toward Cycloheptatriene Containing Nitrogen Heterocyclic Scaffolds. J. Org. Chem., 2021, 86, 4098. DOI 10.1021/acs.joc.0c02928.
  16. Zanakhov T.O., Galenko E.E., Kryukova M.A., Novikov M.S., Khlebnikov A.A., Isomerization of 5-(2H-azirin-2-yl)oxazoles: An atom-economic approach to 4H-pyrrolo[2,3-d]oxazoles. Molecules, 2021, 26, 1881. DOI 10.3390/molecules26071881.
  17. Galenko E.E., Kryukova M.A., Novikov M.S., Khlebnikov A.F., An Isoxazole Strategy for the Synthesis of Fully Substituted Nicotinates. J. Org. Chem., 2021, 86, 6888. DOI 10.1021/acs.joc.1c00286.
  18. Serebryannikova A.V., Galenko E.E., Novikov M.S., Khlebnikov A.F., Product selectivity of thermal Buchner reaction of methyl 2-(3-arylisoxazol-5-yl)-2-diazoacetates with benzene, naphthalene and mesitylene, and ring-opening/closing reaction of products. Tetrahedron, 2021, 88, 132153. DOI 10.1016/j.tet.2021.132153.
  19. Galenko E.E., Kaminskiy N.A., Novikov M.S., Khlebnikov A.F., Synthesis of Water-Soluble α-Aminopyrroles, 1-(2-Amino-1H-pyrrol-3-yl)pyridinium Chlorides. Russ. J. Gen. Chem., 2021, 91, 1424. DOI 10.1134/S1070363221070239.
  20. Efremova M.M., Govdi A.I., Frolova V.V., Rumyantsev A.M., Balova I.A., Design and synthesis of new 5-aryl-4-arylethynyl-1H-1,2,3-triazoles with valuable photophysical and biological properties. Molecules, 2021, 26, 2801. DOI 10.3390/molecules26092801.
  21. Savchuk S.A., Zenkevich I.G., Identification of unknown compound extracted from the hair of exhumed human remains using mass spectrometric and gas chromatographic data. Analitika i Kontrol, 2021, 25, 34. DOI 10.15826/ANALITIKA.2020.25.1.002.
  22. Zenkevich I.G., Nikitina D.A., Deruish A., Formation and Chromatographic Detection of Organic Compound Hydrates. J. Analyt. Chem., 2021, 76, 493. DOI 10.1134/S1061934821040146.
  23. Zenkevich, I.G., Nikitina, D.A., Features of the Recurrent Approximation of Retention Parameters of Polyfunctional Compounds in Reversed-Phase High-Performance Liquid Chromatography. Russ. J. Phys. Chem. A, 2021, 95, 395. DOI 10.1134/S003602442102028X.
  24. Dzhumaev K.K., Zenkevich I.G., Tkachenko K.G., Constituent Composition of Essential Oil from the Aerial Part of Zeravschania regeliana. Chem. Nat. Comp., 2021, 57, 583. DOI 10.1007/s10600-021-03424-9.
  25. Zenkevich I.G., Using Recurrent Dependences to Control, Adjust, and Recover Values of the Physicochemical Properties of Organic Compounds. Russ. J. Phys. Chem. A, 2021, 95, 894. DOI 10.1134/S0036024421040294.
  26. Zenkevich I.G., Recurrent Approximation of the Temperature Dependence of the Solubility of Inorganic Salts in Water. Russ. J. Phys. Chem. A, 2021, 95, 1358. DOI 10.1134/S0036024421060315.
  27. Zenkevich I.G., Determination of Anomalies of Gas Chromatographic Retention Indices for Homologs Based on Their Homologous Increments. Russ. J. Phys. Chem. A, 2021, 95, 1720. DOI 10.1134/S003602442107030X.
  28. Zenkevich I.G., Nikitina D.A., Kornilova T.A., Recurrent Approximation of Retention Parameters of N-Substituted p-Toluenesulfonamides in Reversed-Phase High Performance Liquid Chromatography for Revealing the Formation of Their Hydrates. Russ. J. Phys. Chem. A, 2021, 95, 1931. DOI 10.1134/S0036024421090326.
  29. Minakov D.A., Kartsova L.A., Zakharova A.M., Grinshtein I.L., Minakova O.V., Detailed Hydrocarbon Analysis of Petroleum Products by Gas Chromatography–Mass Spectrometry. J. Analyt. Chem., 2021, 76, 834. DOI 10.1134/S106193482107011X.
  30. Kravchenko A.V., Kolobova E.A., Kartsova L.A., Usage of 3-methyl-1-β-cyclodextrinimidazole tosylate for electrophoretic separation and preconcentration of corticosteroids by capillary electrophoresis. Monatshefte fur Chemie, 2021, 152, 1067. DOI 10.1007/s00706-021-02809-4.
  31. Kravchenko A.V., Kartsova L.A., Effect of Modifiers on the Electrophoretic Separation and Intercapillary Preconcentration of Biologically Active Compounds. J. Analyt.l Chem., 2021, 76, 1043. DOI 10.1134/S1061934821090069.
  32. Lukyanov D.A., Konev A.S., Photocatalysts for Reduction of Molecular Oxygen to Hydrogen Peroxide. Springer Series in Chemical Physics, 2021, 125, 45. DOI 10.1007/978-3-030-77646-6_4.
  33. Mosiagin I.P.,Tomashenko O.A.,Spiridonova D.V.,Novikov M.S.,Tunik S.P.,Khlebnikov A.F., Free-radical cyclization approach to polyheterocycles containing pyrrole and pyridine rings. Beilstein J. Org. Chem., 2021, 17, 1490. DOI 10.3762/bjoc.17.105.
  34. Agafonova A.V., Funt L.D., Novikov M.S., Khlebnikov A.F., An isoxazole strategy for the synthesis of alkyl 5-amino-4-cyano-1H-pyrrole-2-carboxylates - versatile building blocks for assembling pyrrolo-fused heterocycles. Org. Biomol. Chem., 2021, 19, 1976. DOI 10.1039/d1ob00053e.
  35. Koronatov A.N., Afanaseva K.K., Sakharov P.A., Rostovskii N.V., Khlebnikov A.F., Novikov M.S., Rh(ii)-Catalyzed denitrogenative 1-sulfonyl-1,2,3-Triazole-1-Alkyl-1,2,3-Triazole cross-coupling as a route to 3-sulfonamido-1: H-pyrroles and 1,2,3-Triazol-3-ium ylides. Org. Chem. Front., 2021, 8, 1474. DOI 10.1039/d0qo01571g.
  36. Sakharov P.А., Novikov M.S., Rostovskii N.V., 2H-Azirines in medicinal chemistry. Chem. Het. Comp., 2021, 57, 512. DOI 10.1007/s10593-021-02934-2.
  37. Strelnikova J.O., Koronatov A.N., Rostovskii N.V., Khlebnikov A.F., Khoroshilova O.V., Kryukova M.A., Novikov M.S., Rhodium-Catalyzed Denitrogenative Diazole-Triazole Coupling toward Aza-Bridged Structures and Imidazole-Based Chelating Ligands. Org. Lett., 2021, 23, 4173. DOI 10.1021/acs.orglett.1c01092.
  38. Golubev A.A., Agafonova A.V. ,Smetanin I.A.,Rostovskii N.V.,Khlebnikov A.F.,Bunev A.S., Novikov M.S., A Hydroxypyrrole Approach to 2,2′-Bi(4-pyrrolin-3-ones) and Pyrrolone-Based α-Amino Esters. J. Org. Chem., 2021, 86, 10368. DOI 10.1021/acs.joc.1c01070.
  39. Efimenko N.I., Tomashenko O.A., Spiridonova D.V., Novikov M.S., Khlebnikov A.F., Nucleophile-Induced Rearrangement of 2H-Azirine-2-carbonyl Azides to 2-(1H-Tetrazol-1-yl)acetic Acid Derivatives. Org. Lett., 2021, 23, 6362. DOI 10.1021/acs.orglett.1c02157.
  40. Tiuftiakov N.Y., Strelnikova J.O., Filippov I.P., Khaidarov A.R., Khlebnikov A.F., Bunev A.S., Novikov M.S., Rostovskii N.V., Rhodium-Catalyzed Synthesis of 2-Aroylpyrimidines via Cascade Heteropolyene Rearrangement. Org. Lett., 2021, 23, 6998. DOI 10.1021/acs.orglett.1c02706.
  41. Klochkova A.A., Rassadin V.A., Sokolov V.V., A Diastereoselective Route to Benzoannelated Bridged Sultams. Synthesis, 2021, in press. DOI 10.1055/a-1531-2176.
  42. Kritchenkov I.S., Solomatina A.I., Kozina D.O., Porsev V.V., Sokolov V.V., Shirmanova M.V., Lukina M.M., Komarova A.D., Shcheslavskiy V.I., Belyaeva T.N., Litvinov I.K., Salova A.V., Biocompatible Ir(III) complexes as oxygen sensors for phosphorescence lifetime imaging. Molecules, 2021, 26, 2898. DOI 10.3390/molecules26102898.
  43. Klochkova A., Bubyrev A., Dar'In D., Bakulina O., Krasavin M., Sokolov V., Straightforward Route to γ-Sultams via Novel Tandem SN/Michael Addition. Synthesis, 2021, 53, 1795. DOI 10.1055/a-1343-9451.
  44. Kuznetsov K.M., Kritchenkov I.S., Shakirova J.R., Gurzhiy V.V., Pavlovskiy V.V., Porsev V.V., Sokolov V.V., Tunik S.P., Red-to-NIR Iridium(III) Emitters: Synthesis, Photophysical and Computational Study, the Effects of Cyclometallating and β-Diketonate Ligands. Eur. J. Inorg. Chem., 2021, 2163. DOI 10.1002/ejic.202100189.
  45. Derkach K.V., Romanova I.V., Bakhtyukov A.A., Morina I.Y., Dar’in D.V., Sorokoumov V.N., Shpakov A.O., The Effect of Low-Molecular-Weight Allosteric Agonist of Luteinizing Hormone Receptor on Functional State of the Testes in Aging and Diabetic Rats. Bull. Exp. Biol. Med., 2021, 171, 81. DOI 10.1007/s10517-021-05177-5.
  46. Wang S., Filatov A.S.,Lozovskiy S.V.,Shmakov S.V., Khoroshilova O.V., Larina A.G., Selivanov S.I., Boitsov V.M., Stepakov A.V., Construction of Spiro[3-azabicyclo[31.0]hexanes] via 1,3-Dipolar Cycloaddition of 1,2-Diphenylcyclopropenes to Ninhydrin-Derived Azomethine Ylides. Int. J. Mol. Sci., 2021, 22, 8264. DOI 10.1055/a-1360-9716.
  47. Wang S., Filatov A.S., Lozovskiy S.V., Shmakov S.V., Khoroshilova O.V., Larina A.G., Selivanov S.I., Boitsov V.M., Stepakov A.V. Construction of Spiro[3-azabicyclo[31.0]hexanes] via 1,3-Dipolar Cycloaddition of 1,2-Diphenylcyclopropenes to Ninhydrin-Derived Azomethine Ylides. Synthesis, 2021, 53, 2114. DOI 10.1055/a-1360-9716.
  48. Danilkina N.A., Govdi A.I., Khlebnikov A.F., Tikhomirov A.O., Sharoyko V.V., Shtyrov A.A., Ryazantsev M.N., Bräse S., Balova I.A., Heterocycloalkynes Fused to a Heterocyclic Core: Searching for an Island with Optimal Stability-Reactivity Balance. J. Am. Chem. Soc., 2021, 143, 16519. DOI: 10.1021/jacs.1c06041.