Печать
Просмотров: 5427

Публикации кафедры

Обновлено

Публикации кафедры 2023 года

  1. Agafonova A. V., Golubev A. A., Smetanin I. A., Khlebnikov A. F., Spiridonova D. V., Novikov M. S. Divergent Synthesis of Pyrazolo[1,5-a]pyridines and Imidazo[1,5-a]pyridines via Reagent-Controlled Cleavage of the C–N or C–C Azirine Bond in 2-Pyridylazirines. Org. Lett. 2023, DOI: 10.1021/acs.orglett.3c02696
  2. Mammeri O. A., Baranov I. M., Ivanov A. Yu., Boyarskaya I. A., Vasilyev A. V. Synthesis of 2-(5H)-furanones by cyclization of alkyl allene carboxylates in triflic acid. Tetrahedron 2023, 146, 133649. DOI: 10.1016/j.tet.2023.133649
  3. Il’in, M.V., Polonnikov, D.A., Novikov, A.S., Sysoeva, A.A., Safinskaya, Y.V., Bolotin, D.S. Influence of Coordination to Silver(I) Centers on the Activity of Heterocyclic Iodonium Salts Serving as Halogen-Bond-Donating Catalysts. ChemPlusChem 2023, e202300304. DOI: 10.1002/cplu.202300304
  4. Pankova, A.S., Golubev, P., Molin, I.A., Rostovskii, N.V. Regioselective Synthesis of 2-Trimethylsilyl-4H-pyran-4-ones from 1-Ethoxy(hydroxy)-5-(trimethylsilyl)pentenynones. Eur. J. Org. Chem. 2023, 26, e202300573. DOI: 10.1002/ejoc.202300573
  5. Vidyakina, A.A., Shtyrov, A.A., Ryazantsev, M.N., Khlebnikov, A. F., Kolesnikov, I. E., Sharoyko, V. V., Spiridonova, D. V., Balova, I. A., Bräse, S., Danilkina, N.A. Development of Fluorescent Isocoumarin-Fused Oxacyclononyne – 1,2,3-Triazole Pairs. Chem. Eur. J. 2023, 29, e202300540. DOI: 10.1002/chem.202300540
  6. Galenko, E.E., Novikov, M.S., Khlebnikov, A.F. [2 + 2] Cycloaddition/Retro-Electrocyclization/Decarboxylation Reaction Sequence: Access to 4-Aminopyridines from Methylideneisoxazolones and Ynamines. J. Org. Chem. 2023, 88, 8854–8864. DOI: 10.1021/acs.joc.3c00654
  7. Silaichev, P.S., Beryozkina, T.V., Ilkin, V., Novikov, M.S., Dehaen, W., Bakulev, V.A. Tandem Cycloaddition of Azides to 3,3-Diaminoacrylonitriles (2-Cyanoacetamidines) and Cornforth-Type Rearrangement as an Approach to 5-Amino-1,2,3-triazole-4-N-substituted Imidamides. J. Org. Chem. 2023, 88, 8163–8174. DOI: 10.1021/acs.joc.3c00151
  8. Vasilchenko, D.S., Agafonova, A.V., Simdianov, I.V., Koronatov, A. N., Sakharov, P.A., Romanenko, I. A., Rostovskii, N.V., Khlebnikov, A.F., Novikov, M.S. 2H-1,2,3-triazole-4-carboxylic acids via Ru(II)-catalyzed rearrangement of 4-hydrazonoisoxazol-5-ones. Tetrahedron Lett. 2023, 123, 154580. DOI: 10.1016/j.tetlet.2023.154580
  9. Zakharov, T.N., Sakharov, P.A., Novikov, M.S., Khlebnikov, A.F., Rostovskii, N.V. Triethylamine-Promoted Oxidative Cyclodimerization of 2H-Azirine-2-carboxylates to Pyrimidine-4,6-dicarboxylates: Experimental and DFT Study. Molecules 2023, 28, 4315. DOI: 10.3390/molecules28114315
  10. Taishev, A.E., Galenko, E.E., Novikov, M.S., Khlebnikov, A.F. Simple Access to Isoxazole-Containing Heterocyclic Hybrids: Isoxazole/Oxazole and Isoxazole/Pyridine. Russ. J. Gen. Chem. 2023, 93, 1246–1260. DOI: 10.1134/s1070363223050250
  11. Titov, G.D., Antonychev, G.I., Novikov, M.S., Khlebnikov, A.F., Rogacheva, E. V., Kraeva, L.A., Rostovskii, N.V. Gold vs Light: Chemodivergent Reactivity of Diazoesters toward 2H-Azirine-2-carboxylic Acids. Org. Lett. 2023, 25, 2707–2712. DOI: 10.1021/acs.orglett.3c00823
  12. Galenko, E.E., Zanakhov, T.O., Novikov, M.S., Khlebnikov, A.F. Metal carbonyl mediated rearrangement of 5-(2-oxoalkyl)-1,2,4-oxadiazoles: synthesis of fully substituted pyrimidines. Org. Biomol. Chem. 2023, 21, 2990–3001. DOI: 10.1039/D3OB00148B
  13. Galenko, E.E., Zanakhov, T.O., Novikov, M.S., Khlebnikov, A.F. Pd-catalyzed heteroannulation of isoxazoles: Convergent synthesis of isoxazolo[5,4-c]quinolones. Tetrahedron Lett. 2023, 114, 154270. DOI: 10.1016/j.tetlet.2022.154270
  14. Agafonova, A.V., Novikov, M.S., Khlebnikov, A.F. 5-Chloroisoxazoles: A Versatile Starting Material for the Preparation of Amides, Anhydrides, Esters, and Thioesters of 2H-Azirine-2-carboxylic Acids. Molecules 2023, 28, 275. DOI: 10.3390/molecules28010275
  15. Govdi, A.I., Anisimov, S.O., Danilkina, N.A., Bunev, A.S., Balova, I.A. Acyclic enediynes fused to triazole and benzothiophene containing propargylamine moieties. Mendeleev Commun. 2023, 33, 328–330. DOI: 10.1016/j.mencom.2023.04.010
  16. Babushkina, A.A., Mikhailov, V.N., Ogurtsova, A.D., Bunev, A. S., Sorokoumov, V.N., Balova, I.A. The Richter reaction in the synthesis of combretastatin analogs. Russ. Chem. Bull. 2023, 72, 1012–1022. DOI: 10.1007/s11172-023-3866-3
  17. Derkach, K.V., Gureev, M.A., Babushkina, A.A., Mikhaylov, V.N., Zakharova, I.O., Bakhtyukov, A.A., Sorokoumov, V.N., Novikov, A.S., Krasavin, M., Shpakov, A.O., Balova, I.A. Dual PTP1B/TC-PTP Inhibitors: Biological Evaluation of 3-(Hydroxymethyl)cinnoline-4(1H)-Ones. Int. J. Mol. Sci. 2023, 24, 4498. DOI: 10.3390/ijms24054498
  18. Efremova, M.M., Rumyantsev, A.M., Babitova, E.S., Ianshina, T.M., Govdi, A.I. Synthesis of 5-ethynylisoxazoles based on 1,3-dipolar cycloaddition reactions of nitrile oxides with conjugated diynes. Russ. Chem. Bull. 2023, 72, 1717–1721. DOI: 10.1007/s11172-023-3952-5
  19. Ianshina, T., Sidorin, A., Petrova, K., Shubert, M., Makeeva, A., Sambuk, E., Govdi, A., Rumyantsev, A., Padkina, M. Effect of Methionine on Gene Expression in Komagataella phaffii Cells. Microorganisms 2023, 11, 877. DOI: 10.3390/microorganisms11040877
  20. Sokolov, A.A., Egorov, D.M., Pronina, Y.A., Ramsh, S.M., Stepakov, A.V. 1,3-Dipolar Cycloaddition of Stable Azomethine Ylide Based on Ninhydrin and L-Proline to Phosphorylated Acetylenes. Russ. J. Gen. Chem. 2023, 93, 1694–1699. DOI: 10.1134/S1070363223070083
  21. Pevzner, L.M., Makhneva, E.A., Shmakov, S.V., Petrov, M.L., Stepakov, A.V., Boitsov, V.M. In Vitro Activity of Organochalcogen Compounds: IV. Synthesis and Cytotoxic Effect of 4-(1,2,3-Thiadiazol-4-yl)furans Against HeLa, Sk-mel-2, and B16 Tumor Cell Lines. Russ. J. Gen. Chem. 2023, 93, 1513–1522. DOI: 10.1134/S1070363223060245
  22. Pevzner, L.M., Ostrovskaya, A.A., Petrov, M.L., Stepakov, A.V. Synthesis of Ethyl 2-Methyl-4-(diethoxyphosphoryl)-4,7-dihydro-5H-thiopyrano[3,4-b]furan-5-carboxylate and Its Functionalization at the Position 3. Russ. J. Gen. Chem. 2023, 93, 827–840. DOI: 10.1134/S1070363223040084
  23. Pronina, Y.A., Stepakov, A.V., Popova, E.A., Boitsov, V.M., Baichurin, R.I., Selivanov, S.I. Diastereomers of Cyclopropa[a]pyrrolizine Spiro-fused with a Benzo[4,5]imidazo[1,2-a]indole Fragment: Structure Determinations Using NMR Methods. Appl. Magn. Reson. 2023 DOI: 10.1007/s00723-023-01608-w
  24. Komolova, D.D., Pronina, Y.A., Lozovskiy, S.V., Selivanov, S.I., Ponyaev, A.I., Filatov, A.S., Boitsov, V.M., Stepakov, A.V. Palladium-Catalyzed Oxidative Cycloaddition of Quinazoline-2,4(1H,3H)-diones and Diarylalkynes via C-H/N-H Activation. Synthesis 2023 DOI: 10.1055/a-2105-2850
  25. Makeeva, D.V., Antipova, K.S., Solovyeva, E.V., Morgacheva, V.P., Kolobova, E.A., Kartsova, L.A. Multilayer Coatings Based On Citrate-Stabilized Gold Nanoparticles and Polydiallyldimethylammonium Chloride for the Electrophoretic Separation of Carboxylic Acids. J. Anal. Chem. 2023, 78, 361–371. DOI: 10.1134/S1061934823030085
  26. Kartsova, L.A., Maliushevska, A.V., Kolobova, E.A. Analytical Capabilities of the Determination of Carbohydrates by Chromatographic and Electrophoretic Methods. J. Anal. Chem. 2023, 78, 144–161. DOI: 10.1134/S1061934823020041
  27. Karpitskiy, D.A., Bessonova, E.A., Shishov, A.Y., Kartsova, L.A. Selective extraction of plant bioactive compounds with deep eutectic solvents: Iris sibirica L. as example. Phytochem. Anal. 2023 DOI: 10.1002/pca.3272
  28. Kravchenko, A.V., Kolobova, E.A., Kechin, A.A., Kartsova, L.A. Development of a capillary electrophoretic method for determination of ketorolac enantiomers in human plasma using cationic β-cyclodextrin derivative as a chiral selector. J. Sep. Sci. 2023, 46, 2200601. DOI: 10.1002/jssc.202200601
  29. Zakusilo, D.N., Evstigneyev, E.I., Ivanov, A.Y., Mazur, A.S., Bessonova, E.A., Mammeri, O.A., Vasilyev, A.V. Structure of oxidized hydrolysis lignin. J. Wood Chem. Technol. 2023, 43, 103–115. DOI: 10.1080/02773813.2023.2187064
  30. Zenkevich, I.G. Linear Correlations of the Gas Chromatographic Retention Indices of Compounds from Various Taxonomic Groups. J. Anal. Chem. 2023, 78, 766–775. DOI: 10.1134/S1061934823040160
  31. Zenkevich, I.G., Deruish, A., Nikitina, D.A. Features of the Dependence of the Retention Indices of Sorbates in Reversed-Phase High-Performance Liquid Chromatography on the Content of Organic Solvents in the Eluent. Russ. J. Phys. Chem. A 2023, 97, 1007–1017. DOI: 10.1134/S0036024423050321
  32. Deruish, A., Karakashev, G.V., Ukolov, A.I., Zenkevich, I.G. Hydrolytic Stability of Unsubstituted Hydrazones of Aromatic Carbonyl Compounds in Reversed-Phase HPLC. J. Anal. Chem. 2023, 78, 222–230. DOI: 10.1134/S106193482302003X
  33. Savina, I.A., Gusev, D.M., Zimina, T.V., Golovanov, A.A., Zenkevich, I.G. Comparison of Gas-Chromatographic Retention Parameters of Aliphatic Enyne Alcohols with the Data for Their Structural Analogues. J. Anal. Chem. 2023, 78, 74–81. DOI: 10.1134/s1061934822120139
  34. Zenkevich, I.G., Baranov, D.A. Gas-Chromatographic Identification of Unusual Unstable Products of the Partial Hydrolysis of Tetraethoxysilane. J. Anal. Chem. 2023, 78, 82–90. DOI: 10.1134/S1061934823010148
  35. Zenkevich, I.G., Derouiche, A., Nikitina, D.A. Evidence for the Hydration of Some Organic Compounds during Reverse-Phase HPLC Analysis. Molecules 2023, 28, 734. DOI: 10.3390/molecules28020734
  36. Ignatova, I.I., Khoroshilova, O.V., Vasilyev, A.V. Aluminium trichloride-promoted tandem hydroarylation–ionic hydrogenation of 3-arylpropynoic acid derivatives and 4-phenylbut-3-yn-2-one. Mendeleev Commun. 2023, 33, 27–29. DOI: 10.1016/j.mencom.2023.01.008
  37. Samandarsangari, M., Kozina, D.O., Sokolov, V.V., Komarova, A.D., Shirmanova, M.V., Kritchenkov, I.S., Tunik, S.P. Biocompatible Phosphorescent O2 Sensors Based on Ir(III) Complexes for In Vivo Hypoxia Imaging. Biosensors 2023, 13, 680. DOI: 10.3390/bios13070680
  38. Novichikhina, N.P., Pantykina, D.A., Shestakov, A.S., Potapov, A.Yu., Ledenyova, I.V., Kuznetsov, M.A., Shikhaliev, K.S. Allylic and Retro-Allylic Rearrangements upon Bromination of 8,9-Substituted 4,4,6-Trimethyl-4H-Pyrrolo[3,2,1-ij]Quinoline-1,2-Diones. New Aspects and Synthetic Applications. ChemistrySelect 2023, 8, e202203981. DOI: 10.1002/slct.202203981
  39. Solovyeva, E.V., Odintsova, O.V., Svinko, V.O., Makeeva, D.V., Danilov, D.V. Hydroxyapatite-nanosilver composites with plasmonic properties for application in surface-enhanced Raman spectroscopy. Mater. Today Commun. 2023, 35, 105908. DOI: 10.1016/j.mtcomm.2023.105908
  40. Vasilchenko, D.S., Novikov, M.S., Rostovskii, N.V. Rh(II)-catalyzed and non-catalytic synthesis of (Z)-ethene-1,2-diamines from 1-tosyl-1,2,3-triazoles and primary anilines. Chem. Heterocycl. Compd. 2023, 59, 666-671. DOI: 10.1007/s10593-023-03252-5
  41. Pankova, A.S., Golubev, P., Molin, I.A., Rostovskii, N.V. Regioselective Synthesis of 2-Trimethylsilyl-4H-pyran-4-ones from 1-Ethoxy(hydroxy)-5-(trimethylsilyl)pentenynones. Eur. J. Org. Chem. 2023, 26, e202300573. DOI: 10.1002/ejoc.202300573
  42. Vasilchenko, D.S., Agafonova, A.V., Simdianov, I.V., Koronatov, A. N., Sakharov, P.A., Romanenko, I. A., Rostovskii, N.V., Khlebnikov, A.F., Novikov, M.S. 2H-1,2,3-triazole-4-carboxylic acids via Ru(II)-catalyzed rearrangement of 4-hydrazonoisoxazol-5-ones. Tetrahedron Lett. 2023, 123, 154580. DOI: 10.1016/j.tetlet.2023.154580
  43. Zakharov, T.N., Sakharov, P.A., Novikov, M.S., Khlebnikov, A.F., Rostovskii, N.V. Triethylamine-Promoted Oxidative Cyclodimerization of 2H-Azirine-2-carboxylates to Pyrimidine-4,6-dicarboxylates: Experimental and DFT Study. Molecules 2023, 28, 4315. DOI: 10.3390/molecules28114315
  44. Titov, G.D., Antonychev, G.I., Novikov, M.S., Khlebnikov, A.F., Rogacheva, E. V., Kraeva, L.A., Rostovskii, N.V. Gold vs Light: Chemodivergent Reactivity of Diazoesters toward 2H-Azirine-2-carboxylic Acids. Org. Lett. 2023, 25, 2707–2712. DOI: 10.1021/acs.orglett.3c00823

Публикации кафедры 2022 года

  1. Merkulova, E.A.; Kolobov, A.V.; Kuznetsov, M.A.; Spiridonova, D.V.; Pankova, A.S. Oxidative addition of N-aminophthalimide to 3,4-dihydro-2H-thiopyrans, their S-oxides, and S,S-dioxides. Tetrahedron Lett. 2022, 94, 153715. doi: 10.1016/j.tetlet.2022.153715.
  2. Androsov, D.V.; Konev, A.S.; Khlebnikov, A.F. Aziridine strategy for stereospecific synthesis of 1′-alkyl/aryl-5′-aryl-2′,5′-dihydropyrrolofullerene-2′-carboxylates and NMR study of hindered 5′-aryl group rotation. Tetrahedron 2022, 111, 132734. doi: 10.1016/j.tet.2022.132734.
  3. Filatov, A.S.; Selivanov, S.I.; Shmakov, S.V.; Larina, A.G.; Boitsov, V.M.; Stepakov, A.V. An Experimental and Theoretical Study of the 1,3-Dipolar Cyclo addition of Alloxan-Derived Azomethine Ylides to Cyclopropenes. Synthesis. 2022, 54, 1803–1816, doi: 10.1055/a-1700-3115.
  4. Filatov, A.S.; Larina, A.G.; Petrov, M.L.; Boitsov, V.M.; Stepakov, A.V. Synthesis of Quinolino[1,2-c]quinazolin-6-one Derivatives via Formal (4+2)-Cycloaddition of Alkenes to Quinazolin-Derived N-Acyliminium Cations: An Experimental and Theoretical Study. Synthesis. 2022, 54, 2395–2414, doi: 10.1055/a-1755-2061.
  5. Zenkevich, I.G.; Arutyunov, Y.I.; Kopytin, K.A.; Mikhailov, I.Y.; Onuchak, L.A. Characteristics of the Anomalous Temperature Dependence of Gas Chromatographic Retention Indices of Polar Compounds on Packed Columns with a Nonpolar Phase. Russ. J. Phys. Chem. A 2022, 96, 654–663, doi: 10.1134/S003602442203030X.
  6. Efremova, M.M.; Rostovskii, N.V. The VIth International Symposium “The Chemistry of Diazo Compounds and Related Systems” (DIAZO 2021). Russ. J. Org. Chem. 2022, 58, 335–351, doi: 10.1134/S1070428022030113.
  7. Popova, E.A.; Pronina, Y.A.; Davtian, A.V.; Nepochatyi, G.D.; Petrov, M.L.; Boitsov, V.M.; Stepakov, A.V. Squaramide-Based Catalysts in Organic Synthesis (A Review). Russ. J. Gen. Chem. 2022, 92, 287–347, doi: 10.1134/S107036322203001X.
  8. Molchanov, A.P.; Efremova, M.M.; Kuznetsov, M.A. Cyclopropenes and methylenecyclopropanes in 1,3-dipolar cycloaddition reactions. Russ. Chem. Bull. 2022, 71, 620–650, doi: 10.1007/s11172-022-3460-z.
  9. Karpitskiy, D.A.; Bessonova, E.A.; Kartsova, L.A.; Tikhomirova, L.I. Development of approach for flavonoid profiling of biotechnological raw materials Iris sibirica L. by HPLC with high-resolution tandem mass spectrometry. Phytochem. Anal. 2022, 33, 869–878, doi: 10.1002/pca.3135.
  10. Stepakov, A.V.; Filatov, A.S.; Boitsov, V.M.; Lozovskiy, S.V. Diastereoselective cycloaddition of tosylpropadiene to azomethine ylides, derived from proline and carbonyl compounds: an experimental and DFT study. Phosphorus, Sulfur Silicon Relat. Elem. 2022, 197, 67–71, doi: 10.1080/10426507.2021.2017436.
  11. Shcherbakov, N.V.; Titov, G.D.; Chikunova, E.I.; Filippov, I.P.; Rostovskii, N.V.; Kukushkin, V.Y.; Dubovtsev, A.Y. Modular approach to non-aromatic and aromatic pyrroles through gold-catalyzed [3 + 2] cycloaddition of 2H-azirines and ynamides. Org. Chem. Front. 2022, 9, 5133–5140, doi: 10.1039/d2qo01105k.
  12. Agafonova, A.V.; Sakharov, P.A.; Smetanin, I.A.; Rostovskii, N.V.; Khlebnikov, A.F.; Novikov, M.S. Stannyl radical-mediated synthesis of 6H-1,3-oxazin-6-ones from 2-acyloxyazirines or whether free radicals can open the azirine ring? Org. Chem. Front. 2022, 9, 4118–4127, doi: 10.1039/d2qo00783e.
  13. Krivolapova, Y.V.; Tomashenko, O.A.; Funt, L.D.; Spiridonova, D.V.; Novikov, M.S.; Khlebnikov, A.F. Azirine-triazole hybrids: selective synthesis of 5-(2H-azirin-2-yl)-, 5-(1H-pyrrol-2-yl)-1H-1,2,3-triazoles and 2-(5-(2H-azirin-2-yl)-1H-1,2,3-triazol-1-yl)pyridines. Org. Biomol. Chem. 2022, 20, 5434–5443, doi: 10.1039/d2ob00908k.
  14. Kochurin, M.A.; Ismagilova, A.R.; Zakusilo, D.N.; Khoroshilova, O.V.; Boyarskaya, I.A.; Vasilyev, A.V. Reactions of linear conjugated dienone structures with arenes under superelectrophilic activation conditions. An experimental and theoretical study of intermediate multicentered electrophilic species. New J. Chem. 2022, 46, 12041–12053, doi: 10.1039/d2nj01828d.
  15. Danilkina, N.A.; Khmelevskaya, E.A.; Lyapunova, A.G.; D’yachenko, A.S.; Bunev, A.S.; Gasanov, R.E.; Gureev, M.A.; Balova, I.A. Functionalized 10-Membered Aza- and Oxaenediynes through the Nicholas Reaction. Molecules 2022, 27, 6071, doi: 10.3390/molecules27186071.
  16. Igushkina, A.V.; Golovanov, A.A.; Vasilyev, A.V. Michael Addition of 3-Oxo-3-phenylpropanenitrile to Linear Conjugated Enynones: Approach to Polyfunctional δ-Diketones as Precursors for Heterocycle Synthesis. Molecules 2022, 27, 1256, doi: 10.3390/molecules27041256.
  17. Kritchenkov, I.S.; Mikhnevich, V.G.; Stashchak, V.S.; Solomatina, A.I.; Kozina, D.O.; Sokolov, V.V.; Tunik, S.P. Novel NIR-Phosphorescent Ir(III) Complexes: Synthesis, Characterization and Their Exploration as Lifetime-Based O2 Sensors in Living Cells. Molecules 2022, 27, 3156, doi: 10.3390/molecules27103156.
  18. Kalyaev, M.V.; Ryabukhin, D.S.; Borisova, M.A.; Ivanov, A.Y.; Boyarskaya, I.A.; Borovkova, K.E.; Nikiforova, L.R.; Salmova, J.V.; Ul’yanovskii, N.V.; Kosyakov, D.S.; Vasilyev, A.V. Synthesis of 3-Aryl-3-(Furan-2-yl)Propanoic Acid Derivatives, and Study of Their Antimicrobial Activity. Molecules 2022, 27, 4612, doi: 10.3390/molecules27144612.
  19. Sakharov, P.A.; Rostovskii, N.V.; Khlebnikov, A.F.; Novikov, M.S. Copper(II)-Catalyzed (3+2) Cycloaddition of 2H-Azirines to Six-Membered Cyclic Enols as a Route to Pyrrolo[3,2-c]quinolone, Chromeno[3,4-b]pyrrole, and Naphtho[1,8-ef]indole Scaffolds. Molecules 2022, 27, 5681, doi: 10.3390/molecules27175681.
  20. Govdi, A.I.; Tokareva, P.V.; Rumyantsev, A.M.; Panov, M.S.; Stellmacher, J.; Alexiev, U.; Danilkina, N.A.; Balova, I.A. 4,5-Bis(arylethynyl)-1,2,3-triazoles — A New Class of Fluorescent Labels: Synthesis and Applications. Molecules 2022, 27, 3191, doi: 10.3390/molecules27103191.
  21. Gholinejad, M.; Shojafar, M.; Sansano, J.M.; Mikhaylov, V.N.; Balova, I.A.; Khezri, R. Hyperbranched polymer immobilized palladium nanoparticles as an efficient and reusable catalyst for cyanation of aryl halides and reduction of nitroarenes. J. Organomet. Chem. 2022, 970–971, doi: 10.1016/j.jorganchem.2022.122359.
  22. Firsov, A.; Bakulina, O.; Dar’in, D.; Sokolov, V.V.; Krasavin, M. Synthesis of γ-Sultam-Annelated δ-Lactams via the Castagnoli–Cushman Reaction of Sultam-Based Dicarboxylic Acids. J. Org. Chem. 2022, 87, 1537–1540, doi: 10.1021/acs.joc.1c02456.
  23. Ilkin, V.G.; Filimonov, V.O.; Seliverstova, E.A.; Novikov, M.S.; Beryozkina, T.V.; Gagarin, A.A.; Belskaya, N.P.; Muthipeedika, N.J.; Bakulev, V.A.; Dehaen, W. Thioisomünchnones versus Acrylamides via Copper-Catalyzed Reaction of Thioamides with Diazocarbonyl Compounds. J. Org. Chem. 2022, 87, 12196–12213, doi: 10.1021/acs.joc.2c01352.
  24. Filippov, I.P.; Agafonova, A.V.; Titov, G.D.; Smetanin, I.A.; Rostovskii, N.V.; Khlebnikov, A.F.; Novikov, M.S. Synthesis of Imidazo[1,2-a]pyridines via Near UV Light-Induced Cyclization of Azirinylpyridinium Salts. J. Org. Chem. 2022, 87, 6514–6519, doi: 10.1021/acs.joc.2c00514.
  25. Galenko, E.E.; Puzyk, A.M.; Novikov, M.S.; Khlebnikov, A.F. An Isoxazole Strategy for Molybdenum-Mediated Synthesis of 5-Mono- and 4,5-Disubstituted 1H-Pyrrole-2,3-diones. J. Org. Chem. 2022, 87, 6459–6470, doi: 10.1021/acs.joc.2c00386.
  26. Filippov, I.P.; Novikov, M.S.; Khlebnikov, A.F.; Rostovskii, N.V. One-Pot Synthesis of Multifunctionalized 1-Pyrrolines from 2-Alkyl-2H-azirines and Diazocarbonyl Compounds. J. Org. Chem. 2022, 87, 8835–8840, doi: 10.1021/acs.joc.2c00977.
  27. Kaminskiy, N.A.; Galenko, E.E.; Kryukova, M.A.; Novikov, M.S.; Khlebnikov, A.F. Reaction of α-Diazopyrroles with Enamines: Synthesis of Pyrrolo[2,1-c][1,2,4]triazines and α-(1,2,5-Triazapenta-1,3-dienyl)pyrroles. J. Org. Chem. 2022, 87, 10485–10492, doi: 10.1021/acs.joc.2c01102.
  28. Pankova, A.S. Two-Step Construction of Thiophene-Oxazole Dyads with Fluorescent Properties by the Ring Expansion of Aziridines. J. Org. Chem. 2022, 87, 11121–11130, doi: 10.1021/acs.joc.2c01365.
  29. Kartsova, L.A.; Moskvichev, D.O. In-Capillary Chiral Derivatization of Amino Acids. J. Anal. Chem. 2022, 77, 618–624, doi: 10.1134/S1061934822050057.
  30. Shmakov, S.V.; Latypova, D.K.; Shmakova, T.V.; Rubinshtein, A.A.; Chukin, M.V.; Zhuravskii, S.G.; Knyazev, N.A.; Stepakov, A.V.; Galagudza, M.M.; Boitsov, V.M. Biological Evaluation of 3-Azaspiro[Bicyclo[3.1.0]Hexane-2,5’-Pyrimidines] as Potential Antitumor Agents. Int. J. Mol. Sci. 2022, 23, 10759, doi: 10.3390/ijms231810759.
  31. Bakhtyukov, A.A.; Derkach, K. V; Sorokoumov, V.N.; Stepochkina, A.M.; Romanova, I. V; Morina, I.Y.; Zakharova, I.O.; Bayunova, L. V; Shpakov, A.O. The effects of separate and combined treatment of male rats with type 2 diabetes with metformin and orthosteric and allosteric agonists of luteinizing hormone receptor on steroidogenesis and spermatogenesis. Int. J. Mol. Sci. 2022, 23, 198, doi: 10.3390/ijms23010198.
  32. Borisova, M.A.; Ryabukhin, D.S.; Yu. Ivanov, A.; Boyarskaya, I.A.; Shabalin, D.A.; Zelenkov, L.E.; Yu. Schmidt, E.; Trofimov, B.A.; Vasilyev, A.V. Transformations of 5-Hydroxy-1-pyrrolines in Strong Brønsted Acids: Experimental and Theoretical Study of Intermediate Cationic Species. Eur. J. Org. Chem. 2022, 2022, e202200468, doi: 10.1002/ejoc.202200468.
  33. Bakhtyukov, A.A.; Derkach, K. V; Fokina, E.A.; Sorokoumov, V.N.; Zakharova, I.O.; Bayunova, L. V; Shpakov, A.O. Development of Low-Molecular-Weight Allosteric Agonist of Thyroid-Stimulating Hormone Receptor with Thyroidogenic Activity. Dokl. Biochem. Biophys. 2022, 503, 67–70, doi: 10.1134/S1607672922020016.
  34. Baykov, S.; Tarasenko, M.; Kotlyarova, V.; Shetnev, A.; Zelenkov, L.E.; Boyarskaya, I.A.; Boyarskiy, V.P. 2-(1,2,4-Oxadiazol-5-yl)aniline as a New Scaffold for Blue Luminescent Materials. ChemistrySelect 2022, 7, e202201201, doi: 10.1002/slct.202201201.
  35. Penney, A.A.; Efremova, M.M.; Molchanov, A.P.; Kryukova, M.A.; Kudinov, A.Y.; Bunev, A.S.; Keresten, V.M.; Kuznetsov, M.A. 1,3-Dipolar versus Nucleophilic Reactivity of Diaziridines Based on 3,4-Dihydroisoquinoline toward Aryl Iso(thio)cyanates. ChemistrySelect 2022, 7, e202202627, doi: 10.1002/slct.202202627.
  36. Derkach, K. V; Fokina, E.A.; Bakhtyukov, A.A.; Sorokoumov, V.N.; Stepochkina, A.M.; Zakharova, I.O.; Shpakov, A.O. The Study of Biological Activity of a New Thieno[2,3-d]-Pyrimidine-Based Neutral Antagonist of Thyrotropin Receptor. Bull. Exp. Biol. Med. 2022, 172, 713–717, doi: 10.1007/s10517-022-05462-x.
  37. Zharskaia, N.A.; Solomatina, A.I.; Liao, Y.-C.; Galenko, E.E.; Khlebnikov, A.F.; Chou, P.-T.; Chelushkin, P.S.; Tunik, S.P. Aggregation-Induced Ignition of Near-Infrared Phosphorescence of Non-Symmetric [Pt(C^N*N’^C’)] Complex in Poly(caprolactone)-based Block Copolymer Micelles: Evaluating the Alternative Design of Near-Infrared Oxygen Biosensors. Biosensors 2022, 12, 695, doi: 10.3390/bios12090695.
  38. Zanakhov, T.O.; Galenko, E.E.; Novikov, M.S.; Khlebnikov, A.F. An isoxazole strategy for the synthesis of 4-oxo-1,4-dihydro-pyridine-3-carboxylates. Beilstein J. Org. Chem. 2022, 18, 738–745, doi: 10.3762/bjoc.18.74.
  39. Filatov, A.S.; Khoroshilova, O.V.; Larina, A.G.; Boitsov, V.M.; Stepakov, A.V. Synthesis of bis-spirocyclic derivatives of 3-azabicyclo[3.1.0]hexane via cyclopropene cycloadditions to the stable azomethine ylide derived from Ruhemann’s purple. Beilstein J. Org. Chem. 2022, 18, 769–780, doi: 10.3762/bjoc.18.77.
  40. Kalinichev, A.V.; Kravchenko, A.V.; Gryazev, I.P.; Kechin, A.A.; Karpukhin, O.R.; Khairullina, E.M.; Kartsova, L.A.; Golovkina, A.G.; Kozynchenko, V.A.; Peshkova, M.A.; et al. Classification of ballpoint pen inks based on selective extraction and subsequent digital color and cluster analyses. Analyst 2022, 147, 3055–3064, doi: 10.1039/d2an00482h.
  41. Makeeva, D.V.; Antipova, K.S.; Kartsova, L.A. Electrophoretic determination of carboxylic acids in blood serum with intracapillary concentration. Anal. i Kontrol 2022, 26, 13–20, doi: 10.15826/analitika.2022.26.1.001.
  42. Zenkevich, I.G.; Derouiche, A.; Nikitina, D.A. Important features of retention indices determination in reversed-phase high performance liquid chromatography. Anal. i Kontrol 2022, 26, 57–63, doi: 10.15826/analitika.2022.26.1.007.
  43. Zenkevich, I.G.; Derouiche, A. Analytical aspects of organic compounds retention indice dependence in reversed phase HPLC on the content of methanol in eluent. Anal. i Kontrol 2022, 26, 41–48, doi: 10.15826/analitika.2022.26.1.004.
  44. Kasatkina, S.O.; Geyl, K.K.; Baykov, S.V.; Novikov, M.S.; Boyarskiy, V.P. “Urea to Urea” Approach: Access to Unsymmetrical Ureas Bearing Pyridyl Substituents. Adv. Synth. Catal. 2022, 364, 1295–1304, doi: 10.1002/adsc.202101490.
  45. Sakharov, P.A.; Novikov, M.S.; Nguyen, T.K.; Kinzhalov, M.A.; Khlebnikov, A.F.; Rostovskii, N.V. Blue Light-Promoted Cross-Coupling of α-Diazo Esters with Isocyanides: Synthesis of Ester-Functionalized Ketenimines. ACS Omega 2022, 7, 9071–9079, doi: 10.1021/acsomega.2c00367.
  46. Babushkina, A.A.; Mikhaylov, V.N.; Novikov, A.S.; Sorokoumov, V.N.; Gureev, M.A.; Kryukova, M.A.; Shpakov, A.O.; Balova, I.A. Synthesis , X-ray and DFT studies of 6-halo-3-(hydroxymethyl)cinnolin-4(1H)-ones. Chem. Heterocycl. Compd. 2022, 58, 432–437.
  47. Strashkov, D.M., Zavyalov, K.V., Sakharov, P.A., Agafonova, A.V., Rostovskii, N.V., Khlebnikov, A.F., Novikov, M.S. Rhodium-catalyzed migrative annulation and olefination of 2-aroylpyrroles with diazoesters. Org. Chem. Front. 2023, 10, 506–513. DOI: 10.1039/D2QO01759H.
  48. Karcev, D.D., Efremova, M.M., Molchanov, A.P., Rostovskii, N.V., Kryukova, M.A., Bunev, A.S., Khochenkov, D.A. Selective and Reversible 1,3-Dipolar Cycloaddition of 2-(2-Oxoindoline-3-ylidene)acetates with Nitrones in the Synthesis of Functionalized Spiroisoxazolidines. Int. J. Mol. Sci. 2022, 23, 12639. DOI: 10.3390/ijms232012639.
  49. Strashkov, D.M., Zavyalov, K.V., Sakharov, P.A., ...Khlebnikov, A.F., Novikov, M.S. Rhodium-catalyzed migrative annulation and olefination of 2-aroylpyrroles with diazoesters. Org. Chem. Front. 2022, 10, 506–513. DOI: 10.1039/D2QO01759H
  50. Karcev, D.D., Efremova, M.M., Molchanov, A.P., ...Bunev, A.S., Khochenkov, D.A. Selective and Reversible 1,3-Dipolar Cycloaddition of 2-(2-Oxoindoline-3-ylidene)acetates with Nitrones in the Synthesis of Functionalized Spiroisoxazolidines. Int. J. Mol. Sci. 2022, 23, 12639. DOI: 10.3390/ijms232012639

Публикации кафедры 2021 года

  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: 10.1002/ejic.202000827.
  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.

Публикации кафедры 2020 года

  1. Rostovskii N. V., Koronatov A. N., Sakharov P. A., Agafonova A. V., Novikov M. S., Khlebnikov A. F., Rogacheva, E. V., Kraeva, L.A., Azirine-containing dipeptides and depsipeptides: Synthesis, transformations and antibacterial activity. Org. Biomol. Chem. 2020, 18, 9448–9460. DOI: 10.1039/d0ob02023k.
  2. Strelnikov A. A., Konev A. S., Levin O. V., Khlebnikov A. F., Iwasaki A., Yamanouchi K., Tkachenko, N. V., Switching Competition between Electron and Energy Transfers in Porphyrin-Fullerene Dyads J. Phys. Chem. B 2020, 124, 10899−10912. DOI: 10.1021/acs.jpcb.0c06931.
  3. Koronatov A. N., Rostovskii N. V., Khlebnikov A. F., Novikov M. S., Synthesis of 3-Alkoxy-4-Pyrrolin-2-ones via Rhodium(II)-Catalyzed Denitrogenative Transannulation of 1H-1,2,3-Triazoles with Diazo Esters. Org. Lett. 2020, 22, 7958−7963. DOI: 10.1021/acs.orglett.0c02893.
  4. Rashevskii A., Bakulina O., Novikov M. S., Dar'in D., Krasavin M., When periphery matters: Enhanced reactivity of 8-oxa-1,4-dithiaspiro[4.5]decane-7,9-dione and 9-oxa-1,5-dithiaspiro[5.5]undecane-8,10-dione in the Castagnoli-Cushman reaction with imines. Tetrahedron Lett. 2020, 61, 152658. DOI: 10.1016/j.tetlet.2020.152658.
  5. Galenko E. E., Shakirova F. M., Bodunov V. A., Novikov M. S., Khlebnikov A. F., 1-(2H-Azirine-2-carbonyl)benzotriazoles: Building blocks for the synthesis of pyrrole-containing heterocycles. Org. Biomol. Chem. 2020, 18, 2283−2296. DOI: 10.1039/D0OB00206B.
  6. Funt L. D., Krivolapova Y. V., Khoroshilova O. V., Novikov M. S., Khlebnikov A. F., 2H-Azirine-2-carbonyl Azides: Preparation and Use as N-Heterocyclic Building Blocks. J. Org. Chem. 2020, 85, 4182−4194. DOI: 10.1021/acs.joc.9b03367.
  7. Galenko E. E., Kryukova M. A., Novikov M. S., Khlebnikov A. F., Synthesis of Bi-, Ter-, and Quaterpyridinecarboxylates via Propargylisoxazole–Pyridine Rearrangement. J. Org. Chem. 2020, 85, 6109−6122. DOI: 10.1021/acs.joc.0c00611.
  8. Shakirova J. R., Shevchenko N. N., Baigildin V. A., Chelushkin P. S., Khlebnikov A. F., Tomashenko O. A., Solomatina A. I., Starova G. L., Tunik S. P., Eu-based Phosphorescence Lifetime Polymer Nanothermometer: a Nanoemulsion Polymerization Approach to Eliminate Quenching of Eu Emission in Aqueous Media. ACS Applied Polymer Materials. 2020, 2, 537−547. DOI: 10.1021/acsapm.9b00952.
  9. Smetanin I. A., Agafonova A. V., Rostovskii N. V., Khlebnikov A. F., Yufit D. S., Novikov M. S., Stereoselective assembly of 3,4-epoxypyrrolines via nucleophilic addition induced domino cyclization of 6-halo-1-oxa-4-azahexatrienes. Org. Chem. Front. 2020, 7, 525−530. DOI: 10.1039/C9QO01401B.
  10. Sakharov P. A., Rostovskii N. V., Khlebnikov A. F., Novikov M. S., Regiodivergent Synthesis of Butenolide-Based α- And β-Amino Acid Derivatives via Base-Controlled Azirine Ring Expansion. Org. Lett. 2020, 22, 3023−3027. DOI: 10.1021/acs.orglett.0c00793.
  11. Filippov I. P., Novikov M. S., Khlebnikov A. F., Rostovskii N. V., Pseudopericyclic Dearomative 1,6-Cyclization of 1-(2-Pyridyl)-2-azabuta-1,3-dienes: Synthesis and Ring–Chain Valence Equilibria of 4H-Pyrido[1,2-a]pyrazines. Eur. J. Org. Chem. 2020, 3688−3698. DOI: 10.1002/ejoc.202000210.
  12. Nguyen T. K., Titov G. D., Khoroshilova O. V., Kinzhalov M. A., Rostovskii N. V., Light-induced one-pot synthesis of pyrimidine derivatives from vinyl azides. Org. Biomol. Chem. 2020, 18, 4971–4982. DOI: 10.1039/D0OB00693A.
  13. Silaichev P. S., Beryozkina T. V., Novikov M. S., Dehaen W., Bakulev V. A., A Base-Controlled Reaction of 2-Cyanoacetamidines (3,3-Diaminoacrylonitriles) with Sulfonyl Azides as a Route to Nonaromatic 4-Methylene-1,2,3-triazole-5-imines. Eur. J. Org. Chem. 2020, 2020, 3688−3698. DOI: 10.1002/ejoc.202000453
  14. Funt L. D., Novikov M. S., Khlebnikov A. F., New applications of pyridinium ylides toward heterocyclic synthesis. Tetrahedron 2020, 76, 131415. DOI: 10.1016/j.tet.2020.131415
  15. Rostovskii N. V., Smetanin I. A., Koronatov A. N., Agafonova A. V., Potapenkov V. V., Khlebnikov A. F., Novikov M. S., Chem. Het. Comp. 2020, 56, 881–887, DOI: 10.1007/s10593-020-02745-x.
  16. Kazakova A.V., Androsov D.V., Konev A.S., Khlebnikov, A.F., Magnesium acetate – an effective electrophilic activator of the carbonyl group in transesterification of dialkylaziridine dicarboxylates. Chem. Het. Comp. 2020, 56, 875−880, DOI: 10.1007/s10593-020-02744-y.
  17. Filippov I. P., Titov G. D., Rostovskii N. V., Recent Advances in Denitrogenative Reactions of Pyridotriazoles. Synthesis 2020, 18, 3564–3576. DOI: 10.1055/s-0040-1707254.
  18. Danilkina N. A., Govdi A. I., Balova I. A., 5-Iodo-1H-1,2,3-triazoles as Versatile Building Blocks. Synthesis 2020, 52, 1874–1896. DOI: 10.1055/s-0039-1690858.
  19. Danilkina N. A., D’yachenko A. S., Govdi A. I., Khlebnikov A. F., Kornyakov I. V., Bräse, S., Balova, I. A. Intramolecular Nicholas Reactions in the Synthesis of Heteroenediynes Fused to Indole, Triazole, and Isocoumarin. J. Org. Chem. 2020, 85, 9001–9014, DOI: 10.1021/acs.joc.0c00930.
  20. Danilkina N. A., Vasileva A. A., Balova I. A., A. E. Favorskii's scientific legacy in modern organic chemistry: Prototropic acetylene - Allene isomerization and the acetylene zipper reaction. Russ. Chem. Rev. 2020, 89, 125−171. DOI: 10.1070/RCR4902.
  21. Mikhaylov V. N., Sorokoumov V. N., Novikov A. S., Melnik M. V., Tskhovrebov A. G., Balova I. A., Intramolecular hydrogen bonding stabilizes trans-configuration in a mixed carbene/isocyanide PdII complexes. J. Organometallic Chem. 2020, 912, 121174. DOI: 10.1016/j.jorganchem.2020.121174.
  22. Gordeychuk D. I., Sorokoumov V. N., Mikhaylov V. N., Panov M. S., Khairullina E. M., Melnik M. V., Kochemirovsky V. A., Balova I. A., Copper-based nanocatalysts produced via laser-induced ex situ generation for homo- and cross-coupling reactions. Chem. Eng. Sci. 2020, 227, 115940. DOI: 10.1016/j.ces.2020.115940.
  23. Mikhaylov V. N., Pavlov A. O., Ogorodnov Y. V., Spiridonova D. V., Sorokoumov V. N., Balova I. A., N-Propargylation and Copper(I)-Catalyzed Azide-Alkyne Cycloaddition as a Convenient Strategy for Directed Post-Synthetic Modification of 4-Oxo-1,4-Dihydrocinnoline Derivatives. Chem. Het. Comp. 2020, 56, 915–922. DOI: 10.1007/s10593-020-02750-0
  24. Derkach K. V., Bakhtyukov A. A., Sorokoumov V. N., Shpakov A. O., New Thieno-[2,3-d]pyrimidine-Based Functional Antagonist for the Receptor of Thyroid Stimulating Hormone. Doklady Biochemistry And Biophysics, 2020, 491, 77–80. DOI: 10.1134/S1607672920020064.
  25. Bakhtyukov A. A., Derkach K. V., Gureev M. A., Dar’in D. V., Sorokoumov V. N., Romanova I. V., Morina I. Y., Stepochkina A. M., Shpakov A. O., Comparative study of the steroidogenic effects of human chorionic gonadotropin and thieno[2,3-d]pyrimidine-based allosteric agonist of luteinizing hormone receptor in young adult, aging and diabetic male rats. Int. J. Mol. Sci. 2020, 21, 1-28. DOI: 10.3390/ijms21207493.
  26. Molchanov A. P., Efremova M. M., Kryukova M. A., Kuznetsov M. A., Selective and reversible 1,3-dipolar cycloaddition of 6-aryl-1,5-diazabicyclo[3.1.0]hexanes with 1,3-diphenylprop-2-en-1-ones under microwave irradiation. Beilstein J. Org. Chem. 2020, 16, 2679–2686. DOI: 10.3762/BJOC.16.218.
  27. Sirotkina E. V., Efremova M. M., Starova G. L., Kuznetsov M. A., Molchanov A. P., Cycloaddition of nitrones to 1,3-diarylpropenones and subsequent transformations of the resulting isoxazolidines. Chem. Het. Comp. 2020, 56, 1193-1201. DOI: 10.1007/s10593-020-02797-z.
  28. Molchanov A. P., Lukina V. M., Efremova M. M., Muryleva A. A., Slita A. V., Zarubaev V. V., The 1,3-dipolar cycloaddition of adamantine-derived nitrones with maleimides. Synth. Commun. 2020, 50, 1367−1374. DOI: 10.1080/00397911.2020.1738494.
  29. Mikherdov A. S., Katkova S. A., Novikov A. S., Efremova M. M., Reutskaya E. Y., Kinzhalov M. A., (Isocyano group)⋯lone pair interactions involving coordinated isocyanides: experimental, theoretical and CSD studies. CrystEngComm 2020, 22, 1154−1159. DOI: 10.1039/C9CE01741K.
  30. Efremova M. M., Molchanov A. P., Novikov A. S., Starova G. L., Muryleva A. A., Slita A. V., Zarubaev V. V., 1,3-Dipolar cycloaddition of N-allyl substituted polycyclic derivatives of isoindole-1,3-dione with nitrones and nitrile oxides: An experimental and theoretical investigation. Tetrahedron. 2020, 76, 131104. DOI: 10.1016/j.tet.2020.131104.
  31. Pankova A. S., Electrophile-Induced Reactions of Cross-Conjugated Enynones in the Synthesis of Heterocycles. Chem. Het. Comp. 2020, 56, 829−836. DOI: 10.1007/s10593-020-02739-9
  32. Kritchenkov I. S., Elistratova A. A., Sokolov V. V., Chelushkin P. S., Shirmanova M. V., Lukina M. M., Dudenkova V. V., Shcheslavskiy V. I., Kalinina S., Reeß K., Rück A., Tunik S. P., A biocompatible phosphorescent Ir(iii) oxygen sensor functionalized with oligo(ethylene glycol) groups: Synthesis, photophysics and application in PLIM experiments. New J. Chem. 2020, 44, 10459–10471. DOI: 10.1039/d0nj01405b.
  33. Shakirova J. R., Hendi Z., Zhukovsky D. D., Sokolov V. V., Jamali S., Pavlovskiy V. V., Porsev V. V., Evarestov R. A., Tunik S. P., Inorg. Chim. Acta 2020, 511, 119776. DOI: 10.1016/j.ica.2020.119776.
  34. Igushkina A. V., Golovanov A. A., Boyarskaya I. A., Kolesnikov I. E., Vasilyev A. V., Stereoselective Synthesis of Multisubstituted Cyclohexanes by Reaction of Conjugated Enynones with Malononitrile in the Presence of LDA. Molecules, 2020, 25. DOI: 10.3390/molecules25245920
  35. Ismagilova A. R., Zakusilo D. N., Osetrova L. V., Vasilyev A. V., Reaction of 5-phenylpenta-2,4-dienoic acid with benzene in trifluoromethanesulfonic acid. Russ. Chem. Bull. 2020, 69, 1928-1932. DOI: 10.1007/s11172-020-2980-7.
  36. Zaitceva O., Louis B., Beneteau V., Pale P., Shanmugam S., Evstigneyev E. I., Vasiliev A. V., Post-modified FAU zeolites as efficient catalysts for the synthesis of coumarins. Catalysis Today, 2020, in press. DOI: 10.1016/j.cattod.2020.06.081.
  37. Zaitceva O. A., Beneteau V., Ryabukhin D. S., Louis B., Vasilyev A. V., Pale P., Zeolite-promoted synthesis of coumarins and thiocoumarins. ChemCatChem 2020, 12, 326−333. DOI: 10.1002/cctc.201901384.
  38. Zaitceva O. A., Beneteau V., Ryabukhin D. S., Eliseev I. I., Kinzhalov M. A., Louis B., Vasilyev A. V., Pale P., Cyclization of aryl 3-aryl propynoates into 4-arylcoumarines catalyzed by cyclometalated Platinum(II) complexes. Tetrahedron 2020, 76, 131029. DOI: 10.1016/j.tet.2020.131029.
  39. Khoroshilova O. V., Vasilyev A. V., Generation and NMR study of short-lived and reactive trifluoroalkyl carbocations of the α-halogenothiophene series in Brønsted superacids: reactions of the cations with arenes. J. Org. Chem. 2020, 85, 5872−5883. DOI: 10.1021/acs.joc.0c00170.
  40. Gorbunova Y., Zakusilo D. N., Boyarskaya I. A., Vasilyev A. V. Reactions of 3-arylpropenenitriles with arenes under superelectrophilic activation conditions: hydroarylation of the carbon-carbon double bond followed by cyclization into 3-arylindanones. Tetrahedron, 2020, 76, 131264. DOI: 10.1016/j.tet.2020.131264.
  41. Lozovskiy S. V., Vasilyev A. V., Catalyst-Free Preparation of Perfluoroalkyl-Phosphoryl Substituted Furans from 1-Perfluoroalkyl 1,3-Diketones in Two Steps. Adv. Synth. Catal., 2020, 362, 3121−3125. DOI: 10.1002/adsc.202000534.
  42. Borisova M. А., Ryabukhin D. S., Vasilyev, A. V., Reactions of quinoline-2(6,8)-carbaldehydes with arenes by the action of various Brønsted or Lewis acids: synthesis of diarylmethylquinolines. Chem. Het. Comp. 2020, 56, 964–967. DOI: 10.1007/s10593-020-02759-5.
  43. Zalivatskaya A. S., Golovanov A. А., Vasilyev A. V., Cyclization of 1-Aryl-5-Phenylpent-4-en-2-yn-1-Ones to 2,3-Dihydropyran-2-Ones in Trifluoromethanesulfonic Acid. Chem. Het. Comp. 2020, 56, 953–956. DOI: 10.1007/s10593-020-02756-8.
  44. Afanasenko A. M., Chulkova T. G., Boyarskaya I. A., Islamova R. M., Legin A. A., Keppler B. K., Selivanov S. I., Vereshchagin A. N., Elinson M. N., Haukka M., C,N-chelated diaminocarbene platinum(II) complexes derived from 3,4-diaryl-1H-pyrrol-2,5-diimines and cis-dichlorobis(isonitrile)platinum(II): Synthesis, cytotoxicity, and catalytic activity in hydrosilylation reactions. J. Organomet. Chem. 2020, 923, 121435. DOI: 10.1016/j.jorganchem.2020.121435
  45. Remizov Y. O., Kornev A. A., Pevzner L. M., Petrov M. L., Boitsov V. M., Stepakov A.V., In Vitro Activity of Organochalcogen Compounds: I. Cytotoxic Effect of 4-(1,2,3-Thiadiazol-4-yl)furans Against K562 and HeLa Tumor Cell Lines. Russ. J. Gen. Chem. 2020, 90, 2208–2213. DOI: 10.1134/S1070363220110328.
  46. Popova E. A., Kornev A. A., Shmakov S. V., Nepochatyi G. D., Kotyunina O. A., Petrov M. L., Boitsov V. M., Stepakov A. V., In Vitro Activity of Organochalcogen Compounds: II. Cytotoxic Effect of 2-Aminobenzo[b]thiophenes Against K562 and HeLa Tumor Cell Lines. Russ. J. Gen. Chem. 2020, 90, 2214–2218. DOI: 10.1134/S107036322011033X.
  47. Lenshmidt L. V., Ledovskaya M. S., Larina A. G., Filatov A. S., Chakchir O. B., Uspenskii A. A., Stepakov A. V., Synthesis of Isoxazolo[5',4':3,4]pyrrolo[1,2-a]azepines via N-Acyliminium Cyclization. Russ. J. Org. Chem. 2020, 56, 234–245. DOI: 10.1134/S1070428020020098.
  48. Selivanov S. I., Wang S., Filatov A. S., Stepakov A. V., NMR Study of Spatial Structure and Internal Dynamic of Adducts of Ninhydrin-Derived Azomethine Ylide with Cyclopropenes. Applied Magnetic Resonance 2020, 51, 165–182. DOI: 10.1007/s00723-019-01178-w.
  49. Stepanova O. V., Pevzner L. M., Petrov M. L., Stepanova N. P., Sokolova N. B., Stepakov, A. V., Synthesis of 4-(2-Fluoro-4-hydroxyphenyl)-1,2,3-thia- and -Selenadiazoles and Glycosides on Their Base. Russ. J. Gen. Chem. 2020, 90, 1241–1248. DOI: 10.1134/S1070363220070117
  50. Kartsova L. A., Makeeva D. V., Bessonova E. A., Current Status of Capillary Electrophoresis. J. Analyt. Chem. 2020, 75, 1497−1513. DOI: 10.1134/S1061934820120084.
  51. Kravchenko A., Kolobova E., Kartsova L., Multifunction covalent coatings for separation of amino acids, biogenic amines, steroid hormones, and ketoprofen enantiomers by capillary electrophoresis and capillary electrochromatography. SEPARATION SCIENCE PLUS 2020, 3, 102−111. DOI: 10.1002/sscp.201900098.
  52. Kartsova L., Moskvichev D., Bessonova E., Peshkova M. Imidazolium Ionic Liquids in Microemulsion Electrokinetic Chromatography for Separation of Polyphenol Antioxidants Chromatographia 2020, 83, 1001–1008. DOI: 10.1007/s10337-020-03921-z.
  53. Polikarpova D., Makeeva D., Kolotilina N., Dolgonosov A., Peshkova M., Kartsova L., Nanosized cation exchanger for the electrophoretic separation and preconcentration of catecholamines and amino acids. Electrophoresis 2020, 41, 1031−1038. DOI: 10.1002/elps.201900416.
  54. Makeeva D., Polikarpova D., Demyanova E., Roshchina E., Vakhitov T., Kartsova L., Determination of native amino acids and lactic acid in Lactobacillus helveticus culture media by capillary electrophoresis using Cu2+ and β-cyclodextrins as additives. J. Chromatogr. B 2020, 1156, 122304. DOI: 10.1016/j.jchromb.2020.122304.
  55. Deev V., Solovieva S., Andreev E., Protoshchak V., Karpushchenko E., Sleptsov A., Kartsova L., Bessonova E., Legin A., Kirsanov D., Prostate cancer screening using chemometric processing of GC–MS profiles obtained in the headspace above urine samples. J. Chromatogr. B 2020, 1155, 122298. DOI: 10.1016/j.jchromb.2020.122298.
  56. Bessonova E. A., Deev V. A., Kartsova L. A., Dispersive Liquid–Liquid Microextraction of Pesticides Using Ionic Liquids As Extractants. J. Analyt. Chem. 2020, 75, 991–999. DOI: 10.1134/S1061934820080043
  57. Tiuftiakov N. Y., Kalinichev A. V., Rudenko I. V., Bessonova E. A., Kartsova L. A., Peshkova M. A., pH-dependent distribution of the indicator dye tetrabromophenolphthalein ethyl ester between aqueous solution and plasticized polymeric phase: Predicting the lifetime of ion-selective optical sensors. Colloids and Interface Science Comm. 2020, 37, 100295. DOI: 10.1016/j.colcom.2020.100295.
  58. Shishov A., Gerasimov A., Nechaeva D., Volodina N., Bessonova E., Bulatov A., An effervescence-assisted dispersive liquid–liquid microextraction based on deep eutectic solvent decomposition: Determination of ketoprofen and diclofenac in liver. Microchem. J. 2020, 156, 104837. DOI: 10.1016/j.microc.2020.104837.
  59. Eliseenkov E. V., Zenkevich I. G., Characterization of Substituted 1,3-Dioxolanes and 1,3-Dioxanes by Gas Chromatography–Mass Spectrometry. J. Analyt. Chem. 2020, 75, 1790–1807. DOI: 10.1134/S1061934820140087
  60. Zenkevich I. G., Eliseenkov E. V., Principles of Controlling the Correctness of Gas-Chromatographic Retention Indices of Previously Uncharacterized Analytes (Based on an Example of 2-Aryl-1,3-Dioxolanes and 2-Aryl-1,3-Dioxanes). J. Analyt. Chem. 2020, 75, 1608–1625. DOI: 10.1134/S1061934820120151
  61. Zenkevich I. G., Specific Features of the Gas Chromatography–Mass Spectrometry Identification of Monoalkyl Phthalates. J. Analyt. Chem. 2020, 75, 1322–1329.
  62. Zenkevich I. G., Leleev E., Specific Features of the Gas Chromatographic Analysis of Samples in High-Boiling Solvents Using Capillary Columns with a Low Split Ratio of the Carrier Gas Flow. J. Analyt. Chem. 2020, 75, 73–83. DOI: 10.1134/S1061934820010165.
  63. Zenkevich I. G., Lukina V. M. Characteristic Features of the Gas Chromatographic Separation of Tautomers of Ethyl Acetoacetate. Russ. J. Phys. Chem. A 2020, 94, 1214–1223. DOI: 10.1134/S0036024420060357.
  64. Zenkevich I. G., Desyatova A. I., Modification of inertness test for gas chromatographic systems. Analitika i Kontrol 2020, 24, 133–141. DOI: 10.15826/analitika.2020.24.2.004.
  65. Vasilchenko, D.S., Novikov, M.S., Rostovskii, N.V. Rh(II)-catalyzed and non-catalytic synthesis of (Z)-ethene-1,2-diamines from 1-tosyl-1,2,3-triazoles and primary anilines. Chem. Heterocycl. Compd. 2023, 59, 666-671. DOI: 10.1007/s10593-023-03252-5
  66. Pankova, A.S., Golubev, P., Molin, I.A., Rostovskii, N.V. Regioselective Synthesis of 2-Trimethylsilyl-4H-pyran-4-ones from 1-Ethoxy(hydroxy)-5-(trimethylsilyl)pentenynones. Eur. J. Org. Chem. 2023, 26, e202300573. DOI: 10.1002/ejoc.202300573
  67. Vasilchenko, D.S., Agafonova, A.V., Simdianov, I.V., Koronatov, A. N., Sakharov, P.A., Romanenko, I. A., Rostovskii, N.V., Khlebnikov, A.F., Novikov, M.S. 2H-1,2,3-triazole-4-carboxylic acids via Ru(II)-catalyzed rearrangement of 4-hydrazonoisoxazol-5-ones. Tetrahedron Lett. 2023, 123, 154580. DOI: 10.1016/j.tetlet.2023.154580
  68. Zakharov, T.N., Sakharov, P.A., Novikov, M.S., Khlebnikov, A.F., Rostovskii, N.V. Triethylamine-Promoted Oxidative Cyclodimerization of 2H-Azirine-2-carboxylates to Pyrimidine-4,6-dicarboxylates: Experimental and DFT Study. Molecules 2023, 28, 4315. DOI: 10.3390/molecules28114315
  69. Titov, G.D., Antonychev, G.I., Novikov, M.S., Khlebnikov, A.F., Rogacheva, E. V., Kraeva, L.A., Rostovskii, N.V. Gold vs Light: Chemodivergent Reactivity of Diazoesters toward 2H-Azirine-2-carboxylic Acids. Org. Lett. 2023, 25, 2707–2712. DOI: 10.1021/acs.orglett.3c00823
  70. Strashkov, D.M., Zavyalov, K.V., Sakharov, P.A., ...Khlebnikov, A.F., Novikov, M.S. Rhodium-catalyzed migrative annulation and olefination of 2-aroylpyrroles with diazoesters. Org. Chem. Front. 2022, 10, 506–513. DOI: 10.1039/D2QO01759H
  71. Karcev, D.D., Efremova, M.M., Molchanov, A.P., ...Bunev, A.S., Khochenkov, D.A. Selective and Reversible 1,3-Dipolar Cycloaddition of 2-(2-Oxoindoline-3-ylidene)acetates with Nitrones in the Synthesis of Functionalized Spiroisoxazolidines. Int. J. Mol. Sci. 2022, 23, 12639. DOI: 10.3390/ijms232012639