FershtatLab

2022


  1. Alexander A.Larin, Alexander V.Shaferov, Konstantin A.Monogarov, Dmitry B.Meerov, Alla N.Pivkina, Leonid L.Fershtat. Novel energetic oxadiazole assemblies. Mendeleev Communications (2022) 32(1):111-113. DOI: 10.1016/j.mencom.2022.01.036
  2. Alexei N. Izmest'ev, Andrey A. Streltsov,Valentina A. Karnoukhova,Dr. Natalya G. Kolotyrkina, Yurii A. Strelenko, Angelina N. Kravchenko, Galina A. Gazieva. 5-Indolylidene-2-iminothiazolidin-4-ones – Convenient Starting Compounds for Stereoselective Synthesis of Novel Dispirooxindole Derivatives. (2022) ChemistrySelect,Volume 7, Issue 2 DOI:10.1002/slct.202104128.
  3. Leonid I. Belen’kii, Galina Gazieva, Yulia Evdokimenkova, N. O. Soboleva. Chapter Five - The literature of heterocyclic chemistry, Part XIX, 2019. (2022) Advances in Heterocyclic Chemistry 136:225-295. DOI: 10.1016/bs.aihch.2021.09.002
  4. Sergey А. Karalash, Dmitry M. Bystrov, Ivan V. Ananyev, Leonid L. Fershtat. Lewis acid catalyzed condensation of 2-aminohetarene N-oxides with N,N-dimethylformamide dimethyl acetal. Chemistry of Heterocyclic Compounds, 57(11), 1130–1136 DOI: 10.1007/s10593-021-03031-0
  5. Margarita A. Epishina, Alexander S. Kulikov, Leonid L. Fershtat. Revisiting the Synthesis of Functionally Substituted 1,4-Dihydrobenzo[e][1,2,4]triazines. Molecules 2022,27(8), 2575 DOI: 10.3390/molecules27082575
  6. L. L. Fershtat, Synthesis of 1,4-dihydro-1,2,4-benzotriazin-4-yl radicals (microreview). Chemistry of Heterocyclic Compounds 58, (4-5) DOI: 10.1007/s10593-022-03072-z
  7. A. O. Kuptsova, Ekaterina E. Vinogradova, A. N. Kravchenko, Galina A. Gazieva. Methods for substitution of the thioxo group with the oxo group in imidazolidine-2-thione derivatives. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 71(5):885-904. DOI: 10.1007/s11172-022-3488-0
  8. Daniil D. Degtyarev, M. S. Polkovnichenko, Alexander A. Larin, Leonid L. Fershtat. Synthesis of 3,5-difuroxanyl-1,6-dihydro-1,2,4-triazines. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 71(6):1257-1261. DOI: 10.1007/s11172-022-3527-x
  9. Alexander A. Larin, Ivan V. Ananyev, Ekaterina V. Dubasova, Fedor E. Teslenko, Konstantin A. Monogarov, Dmitry V. Khakimov, Chun-lin He, Si-ping Pang, Galina A. Gazieva, Leonid L. Fershtat. Simple and energetic: Novel combination of furoxan and 1,2,4-triazole rings in the synthesis of energetic materials. Energetic Materials Frontiers V. 3 (3), Pages 146-153 DOI: 10.1016/j.enmf.2022.08.002
  10. Vladimir V. Baranov, Tatyana N. Vol'khina, Natalya G. Kolotyrkina, Angelina N. Kravchenko. Synthesis and crystal structures of novel glycoluril carboxylic acids conglomerates. Mendeleev Communications 32(4):537-539. DOI: 10.1016/j.mencom.2022.07.034
  11. Evgeniy V. Ivanov, Elena Y. Lebedeva, Vladimir V. Baranov, Angelina N. Kravchenko. Volume properties of tetramethylenediethylenetetramine (pharmaceutical teotropine) in aqueous solutions between 278.15 and 318.15 K. The Journal of Chemical Thermodynamics 174(6), 106860. DOI: 10.1016/j.jct.2022.106860
  12. Izmestyev A.N., Vladimir A. Motornov, Dmitry B. Vinogradov, Sema L. Ioffe, Angelina N. Kravchenko, Galina A. Gazieva.Tandem Michael addition/elimination – novel reactivity of pyridinium ylides in reaction with electron-deficient alkenes. Organic Chemistry Frontiers 9(18) DOI: 10.1039/D2QO00911K
  13. Alexei N. Izmest’ev, Lada V. Anikina, Igor E. Zanin, Natalya G. Kolotyrkina, Ekaterina S. Izmalkova, Angelina N. Kravchenko, Galina A. Gazieva.Design, synthesis and in vitro evaluation of the hybrids of oxindolylidene and imidazothiazolotriazine as efficient antiproliferative agents. New Journal of Chemistry 46(24) DOI: 10.1039/D2NJ01454H
  14. Egor S. Zhilin, Ivan V. Ananyev, Alla N Pivkina, Leonid L. Fershtat. Renaissance of Dinitroazetidine: Novel Hybrid Energetic Boosters and Oxidizers. Dalton Transactions, 51, 14088-14096 DOI: 10.1039/D2DT02445D
  15. Leonid L. Fershtat. Recent advances in the synthesis and performance of 1,2,4,5-tetrazine-based energetic materials. FirePhysChem, In press DOI: 10.1039/D2DT02445D
  16. Dmitry M. Bystrov, Alla N. Pivkina, Leonid L. Fershtat An Alliance of Polynitrogen Heterocycles: Novel Energetic Tetrazinedioxide-Hydroxytetrazole-Based Materials Molecules 27(18):5891 DOI: 10.3390/molecules27185891
  17. Alexander A. Larin, Alla N. Pivkina, Ivan V. Ananyev, Dmitry V. Khakimov, Leonid L. Fershtat. Novel family of nitrogen-rich energetic (1,2,4-triazolyl) furoxan salts with balanced performance. Frontiers in Chemistry, 10, online DOI: 10.3389/fchem.2022.1012605
  18. Alexei N. Izmestyev, Angelina N. Kravchenko, Galina A. Gazieva. Synthesis of 7-oxindolylidene-3a,9a-diphenylimidazothiazolo[2,3-c][1,2,4]triazines by skeletal rearrangement of their [3,2-b]-fused isomers. Mendeleev Communications 32(5):678-679 DOI: 10.1016/j.mencom.2022.09.037
  19. Rational Screening of Cocrystals using Thermal Analysis: Benchmarking on Energetic Materials. Nikita V. Muravyev, Leonid L. Fershtat, Igor L. Dalinger, Kyrill Yu. Suponitsky, Ivan V. Ananyev, Igor N. Melnikov. Cryst. Growth Des. 2022, 22, 12, 7349–7362. DOI:10.1021/acs.cgd.2c00964
  20. Alexander A. Larin, Leonid L. Fershtat. Energetic heterocyclic N-oxides: synthesis and performance Mendeleev Communications, V.32, I. 6, P. 703-713. DOI:10.1016/j.mencom.2022.11.001
  21. (2‐Vinyltetrazolyl)furoxans as New Potential Energetic Monomers. Daniil A. Chaplygin, Alexander A. Larin, Dmitry B. Meerov, Konstantin A. Monogarov, Dmitry K. Pronkin, Alla N. Pivkina, Leonid L. Fershtat. ChemPlusChem, 2022 87(12). DOI: 10.1002/cplu.202200365
  22. Synthesis, Structure and Stereochemistry of Dispirocompounds Based on Imidazothiazolotriazine and Pyrrolidineoxindole. Alexei N. Izmest’ev ,Valentina A. Karnoukhova, Alexander A. Larin, Angelina N. Kravchenko, Leonid L. Fershtat, Galina A. Gazieva. Int. J. Mol. Sci. 2022, 23(22), 13820. DOI: 10.3390/ijms232213820
  23. The Chemo- and Regioselectivity of the Cyclization of Thiosemicarbazides with Haloacetic Acids and their Derivatives. Alexei N. Izmest’ev, Andrey А. Streltsov, Angelina N. Kravchenko, Galina А. Gazieva. Chemistry of Heterocyclic Compounds volume 58, pages 483–492 (2022) DOI:10.1007/s10593-022-03117-3
  24. A regioselective synthesis of imidazothiazolotriazines based on the cyclization of imidazotriazinethiones with phenacyl bromides. Dmitry B. Vinogradov, Alexei N. Izmest’ev, Angelina N. Kravchenko, Galina А. Gazieva. Chemistry of Heterocyclic Compounds volume 58, pages 524–530, (2022). DOI: 10.1007/s10593-022-03123-5
  25. Synthesis of S-substituted 5-sulfonylmethyl(ethyl)-1,3,4-thiadiazol-2-amines. Sergei A. Serkov, Natalya V. Sigay, Natalya N. Kostikova, Aleksander E. Fedorov, Anton P. Tyurin, Galina A. Gazieva. Chemistry of Heterocyclic Compounds volume 58, pages 514–517 (2022) DOI : 10.1007/s10593-022-03121-7
  26. Synthesis and antiproliferative activity characterization of new imidazothiazolotriazine oxindolylidene derivatives containing various substituents in the oxindole ring. Alexei N. Izmest’ev, Angelina N. Kravchenko, Galina A. Gazieva Chemistry of Heterocyclic Compounds volume 58, pages 531–538 (2022) DOI: 10.1007/s10593-022-03125-3

2021

  1. A. A. Larin, L. L. Fershtat. High-energy hydroxytetrazoles: design, synthesis and performance. Energetic Materials Frontiers Energetic Materials Frontiers 2,3–13 DOI:10.1016/j.enmf.2021.01.001
  2. A.N Izmest'ev, G.A. Gazieva, N.G. Kolotyrkina, E.D. Daeva, A.N. Kravchenko. Synthesis of 5-arylmethylidene-3-(arylmethylideneamino)thiazolidine-2,4-diones via triazine ring cleavage of tetrahydroimidazothiazolotriazinediones and their reactions with azomethine ylides. Chemistry of Heterocyclic Compounds 56(12). DOI:10.1007/s10593-020-02851-w
  3. Alexander S. Kulikov, Margarita A. Epishina, Egor S. Zhilin, Alexander D. Shuvaev, Leonid L. Fershtat, Nina N. Makhova. Design and synthesis of pyrazolo[3,4-d]pyridazine 5,6-dioxides as novel NO-donors Mendeleev Commun., 2021, 31, 42–45 DOI:10.1016/j.mencom.2021.01.012
  4. Valentina A. Karnoukhova, Vladimir V. Baranov, Anna V. Vologzhanina, Angelina N. Kravchenko and Ivan V. Fedyanin. Self-organization of 1,6-dialkyl-3a,6a-diphenylglycolurils in the crystalline state. CrystEngComm,23, 4312-4319 DOI:10.1039/d1ce00434d
  5. Alexei N. Izmest’ev, a Galina A. Gazieva, Lada V. Anikina, Sergey A. Pukhov, Valentina A. Karnoukhova, Natalya G. Kolotyrkina, Angelina N. Kravchenko. Synthesis and evaluation of the antiproliferative activity of new heterylmethylidene derivatives of imidazothiazolotriazinones. New J. Chem., Available online DOI: 10.1039/d1nj02163j
  6. Nikita V. Muravyev, Dmitry B. Meerov, KonstantinA. Monogarov, Igor N. Melnikov, Ekaterina K. Kosareva, Leonid L. Fershtat, Aleksei B. Sheremetev, Igor L. Dalinger, Igor V. Fomenkov, Alla N. Pivkina. Sensitivity of Energetic Materials: Evidence of Thermodynamic Factor on a Large Array of CHNOFCl Compounds. Chemical Engineering Journal 421,129804 DOI:10.1016/j.cej.2021.129804
  7. Dmitry V. Khakimov,Leonid L. Fershtat, Tatyana S. Pivina, Nina N. Makhova. Nitrodiaziridines: Unattainable yet, but Desired Energetic Materials. J. Phys. Chem. A, 125, 18, 3920–3927 DOI:10.1021/acs.jpca.1c02960
  8. M. D. Vedenyapina, V. V. Kuznetzov, A S. Dmitrenok, M. E. Minyaev, N. N. Makhova, and M. M. Kazakova. Gold anode corrosion in an aqueous solution of 2,2-dimethyl-1,3-diaminopropane. Russ. Chem. Bull. volume 70, p. 735–744. DOI:10.1007/s11172-021-3144-0
  9. Alexei N. Izmest’ev, Dmitry B. Vinogradov , Natalya G. Kolotyrkina , Angelina N. Kravchenko and Galina A. Gazieva. Synthesis of functionalized imidazo[4,5-e]thiazolo[3,2-b]tri- azines by condensation of imidazo[4,5-e]triazinethiones with DMAD or DEAD and rearrangement to imidazo[4,5-e]thiazolo[2,3-c]triazines Beilstein Journal of Organic Chemistry 17(1), p.1141-1148 DOI:10.3762/bjoc.17.87
  10. Sergei А. Serkov , Marina А. Es'kova, Natalya V. Sigay , Natalya N. Kostikova , Tatyana N. Volkhina, Natalya G. Kolotyrkina , Galina А. Gazieva. Synthesis of 1,3-dialkyl-4-[(arylmethylidene)amino]glycolurils. Chemistry of Heterocyclic Compounds, 57(6), 646–655. DOI: 10.1007/s10593-021-02963-x
  11. Leonid Fershtat, Fedor Teslenko. Five-Membered Hetarene N-Oxides: Recent Advances in Synthesis and Reactivity. Synthesis, Available online. DOI: 10.1055/a-1529-7678
  12. E.S. Zhilin, N.E. Ustyuzhanina, L.L. Fershtat, N.E. Nifantiev, N.N. Makhova. Antiaggregant effects of (1,2,5-oxadiazolyl)azasydnone ring assemblies as novel antiplatelet agents. Chemical Biology and Drug Design. DOI:10.1111/cbdd.13918
  13. Alexander A. Larin, Alexander V. Shaferov, Alexander S. Kulikov, Alla N. Pivkina,Konstantin A. Monogarov, Artem O. Dmitrienko, Ivan V. Ananyev, Dmitry V. Khakimov, Leonid L. Fershtat, Nina N. Makhova. Design and Synthesis of Nitrogen‐Rich Azo‐Bridged Furoxanylazoles as High‐Performance Energetic Materials Chemistry- European Journal DOI:10.1002/chem.202101987
  14. Daniil A. Chaplygin, Yaroslav K. Gorbunov, Leonid L.Fershtat Ring Distortion Diversity‐Oriented Approach to Fully Substituted Furoxans and Isoxazoles Asian Journal of Organic Chemistry DOI: 10.1002/ajoc.202100475
  15. Daniil A. Chaplygin, Alexander A. Larin, Nikita V. Muravyev, Dmitry B. Meerov, Ekaterina K. Kosareva, Vitaly G. Kiselev, Alla N. Pivkina,Ivan V. Ananyev, Leonid L. Fershtat. Nitrogen-Rich Metal-Free Salts: a New Look at 5 (Trinitromethyl)tetrazolate Anion as an Energetic Moiety Dalton Transactions DOI: 10.1039/D1DT02688G
  16. Leonid Fershtat, Egor S. Zhilin Recent Advances in the Synthesis and Biomedical Applications of Heterocyclic NO-Donors Molecules 26(18):5705 DOI: 10.3390/molecules26185705
  17. Nikita V.Muravyev, Igor N.Melnikov, Daniil A.Chaplygin, Leonid L.Fershtat, Konstantin A.Monogarov. Two Sides of Thermal Stability of Energetic Liquid: Vaporization and Decomposition of 3-Methylfuroxan Journal of Molecular Liquids, available online DOI: 10.1016/j.molliq.2021.118059
  18. Kseniia YuTitenkova, Alexander V.Shaferov, Alexander A.Larin, Margarita A.Epishina, Alexander S.Kulikov, Ivan V.Ananyev, Leonid L.Fershtat. Tandem acid-promoted intramolecular azide-hydrazone electrocyclization/hydrolysis approach for the synthesis of N-Aminotetrazoles. Tetrahedron, available online DOI: 10.1016/j.tet.2021.132563
  19. Karalash S.A. / S.A. Karalash, D.M. Bystrov, I.V. Ananyev, L.L. Fershtat. Lewis acid-catalyzed condensation of 2-aminohetarene-N-oxides with dimethylformamide dimethylacetal. Chemistry of Heterocyclic Compounds 57(11), 1130–1136.
  20. E.E. Vinogradova, G.A. Gazieva, A.N. Izmest’ev, V.A. Karnoukhova, A.N. Kravchenko. Dimroth-type N/S-interchange of N-aminothioglycolurils in the synthesis of 2-hydrazonoimidazo[4,5-d]thiazolones. RSC Advances– 2021. – Vol. 11.– Issue 45.– p. 28395–28400. DOI:10.1039/D1RA05568B
  21. Egor S. Zhilin, Dmitry B. Meerov, Leonid L. Fershtat. Potassium (3-Methyl-2-oxido-1,2,5-oxadiazol-4-yl)dinitromethanide. Molbank 2021,2021(4), M1301. DOI: 10.3390/M1301
  22. Vladimir V.Baranov, Tatyana N.Vol'khina, Yulia V.Nelyubina, Angelina N.Kravchenko. New aspects of reactions of methyl (thio)ureas with benzil. Mendeleev Communications, Volume 31, Issue 5, 2021, Pages 673-676. DOI:10.1016/j.mencom.2021.09.027

2020

  1. Makhova, N. N., Belen’kii, L. I., Gazieva, G. A., Dalinger, I. L., Konstantinova, L. S., Kuznetsov, V. V., Yarovenko, V. N. , Kravchenko, A.N., Krayushkin, M.M., Rakitin, O.A, Starosotnikov, A.M., Fershtat, L.L., Shevelev S.A., Shirinian V.Z. (2020). Progress in the chemistry of nitrogen-, oxygen- and sulfur-containing heterocyclic systems. Russian Chemical Reviews, 89(1), 55–124. DOI:10.1070/rcr4914
  2. Teslenko, F. E., Churakov, A. I., Larin, A. A., Ananyev, I. V., Fershtat, L. L., Makhova, N. N. (2020). Route to 1,2,4- and 1,2,5-oxadiazole ring assemblies via a one-pot condensation/oxidation protocol. Tetrahedron Letters, Vol. 61- Iss. 13- P.151678. DOI:10.1016/j.tetlet.2020.151678
  3. Zlotin, S.G., Dalinger, I.L., Makhova, N.N., Tartakovskii, V.A. (2020) Nitrocompounds as the core structure of perspective energetic materials and versatile reagents for organic synthesis. Russian Chemical Reviews 89(1) - P.1-54. DOI: 10.1070/RCR4908
  4. Baranov, V.V., Galochkin A.A., Nelyubina Y.V., Kravchenko A.N., Makhova N.N. (2020) Synthesis and Structure of 1-Substituted Semithioglycolurils. Synthesis. 52(17): 2563-2571 DOI: 10.1055/s-0040-1707391
  5. Chaplygin, D.A., Ananyev, I. V., Fershtat, L. L., Makhova, N. N. Divergent Synthesis of Five-Membered Nitrogen Heterocycles via Cascade Reactions of 4-Arylfuroxans. Synthesis. Available online DOI: 10.1055/s-0040-1707393
  6. Larin, A.A., Fershtat, L.L., Makhova, N.N (2020). Tandem reactions of thermolysis and [3+2] cycloaddition in the synthesis of 3-hetaryl-4-nitrofuroxans from 4-nitrofuroxannitrolic acid. Chemistry of Heterocyclic Compounds, 56(5), 607–610. DOI:10.1007/s10593-020-02706-4
  7. Inna N. Kolesnikova, Anatolii N. Rykov, Vladimir V. Kuznetsov, Igor F. Shishkov (2020). Joint gas-phase electron diffraction and quantum chemical study of conformational landscape and molecular structure of sulfonamide drug sulfanilamide. Structural Chemistry 31, pages 1353–1362. DOI : 10.1007/s11224-020-01528-6
  8. A.V.Belyakova, A.A.Oskorbin, V.A.Losev, A.N.Rykov, I.F.Shishkov, L.L.Fershtat, A.A.Larin, V.V.Kuznetsov, N.N.Makhova (2020). The equilibrium molecular structure of 3-methyl-4-nitro- and 4-methyl-3-nitrofuroxans by gas-phase electron diffraction and coupled cluster calculations Journal of Molecular Structure. Volume 1222, p.128856 DOI : 10.1016/j.molstruc.2020.128856
  9. A.A. Larin, A.V. Shaferov, M.A. Epishina, I.N. Melnikov, N.V. Muravyev,I.V. Ananyev, L.L. Fershtat, N.N. Makhova (2020). Pushing the Energy-Sensitivity Balance with High-Performance Bifuroxans ACS Appl. Energy Mater.2020, 3, 8, 7764–7771 DOI: 10.1021/acsaem.0c01162
  10. Leonid I. Belen’kii, G.A. Gazieva, Yulia Evdokimenkova, N. O. Soboleva.(2020) The literature of heterocyclic chemistry, part XVIII, 2018. Advances in Heterocyclic Chemistry, available online. DOI: 10.1016/bs.aihch.2020.01.002
  11. L. V. Anikina, G.A. Gazieva, A. N. Kravchenko. (2020) Nootropic activity of N-(2-acetylaminoethyl)glycolurils. Russian Chemical Bulletin 69(3):563-566 DOI: 10.1007/s11172-020-2799-2
  12. A N. Izmest'ev, G.A. Gazieva, A. N. Kravchenko. (2020) Regioselectivity of (3+2) cycloaddition of azomethine ylides to activated olefins in the synthesis of spiro[oxindole-3,2′-pyrrolidine] derivatives Chemistry of Heterocyclic Compounds 56(3) DOI: 10.1007/s10593-020-02654-z
  13. A.N. Izmest'ev, G.A. Gazieva, V.A. Karnoukhova, A. N. Kravchenko. (2020) Diastereodivergent synthesis of dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties Organic & Biomolecular Chemistry, Available online. DOI: 10.1039/D0OB01628D
  14. E. S. Zhilin, M.S. Polkovnichenko, I.V. Ananyev, L.L. Fershtat, N.N. Makhova. (2020) Novel arylazo‐1,2,5‐oxadiazole photoswitches: synthesis, photoisomerization and NO‐releasing properties. ChemPhotoChem, Available online DOI: 10.1002/cptc.202000157
  15. I. I.Marochkin, V. V.Kuznetsov, Zhi dong Li, A. N.Rykov,N.N.Makhova,I.F.Shishkov Molecular structure of 1,2-diethyldiaziridine studied by gas electron diffraction supported by quantum chemistry calculations Journal of Molecular Structure, V. 1225-p. 129066 DOI:10.1016/j.molstruc.2020.129066
  16. Larin, A.A.; Bystrov, D.M.; Fershtat, L.L.; Konnov, A.A.; Makhova, N.N.; Monogarov, K.A.; Meerov, D.B.; Melnikov, I.N.; Pivkina, A.N.; Kiselev, V.G.; Muravyev, N.V. Nitro-, Cyano-, and Methylfuroxans, and Their Bis-Derivatives: From Green Primary to Melt-Cast Explosives. Molecules 2020 ,25, 5836. DOI:10.3390/molecules25245836
  17. Vedenyapina, M.D., Kuznetsov, V.V., Makhova, N.N.et al. Gold anode corrosion in aqueous solution of 1,2-diaminopropane with formation of colloidal gold nanoparticles. Russ Chem Bull 69,1884–1891 (2020). DOI:10.1007/s11172-020-2974-5
  18. Natalia I. Vikrishchuk, Valerii V. Tkachev, Gennady S. Borodkin, Galina A. Gazieva, Gennady V. Shilov. Synthesis of 1,2,4-triazolo[5′,1′:2,3][1,3]thiazino[6,5-b]indol-10(5H)-ones based on 2-chloro-1H-indole-3-carbaldehyde. Tetrahedron Letters, Volume 61, Issue 45. DOI:10.1016/j.tetlet.2020.152490
  19. D.M. Bystrov, I.V.Ananyev, L.L. Fershtat, N.N. Makhova Direct Synthesis of N -(1,2,5-Oxadiazolyl)hydrazones through a Diazotization/Reduction/Condensation Cascade. The Journal of Organic Chemistry 85(23):15466-15475 DOI:10.1021/acs.joc.0c02243 V.A. Ivolgina, L.D. Popov, G.A.Gazieva, A.N. Kravchenko Protolytic and potential antithyroid properties of thioglycolurils and fused azolo-1,2,4-triazine. Russian Chemical Bulletin 69(11):2215-2221 DOI: 10.1007/s11172-020-3024-z

2019


  1. Bystrov D.M. Fershtat L.L., Makhova N.N. Synthesis and reactivity of aminofuroxans. Chemistry of Heterocyclic Compounds V.55, pages 1143–1164. DOI: 10.1007/s10593-019-02593-4
  2. Ivanov,E.V.,Lebedeva, E. Yu., Batov, D. V., Baranov, V. V., Kravchenko, A. N.. Equimolecular cocrystal of cis- and trans-coordinated N,N′-dimethylglycolurils: Some standard thermodynamic properties in the aqueous solution between 278.15 K and 318.15 K. Journal of Molecular Liquids Vol. 297, P. 111891 DOI:10.1016/j.molliq.2019.111891
  3. A. N. Izmest'ev, N. A. Kim, V. A. Karnoukhova, N. G. Kolotyrkina, A. N. Kravchenko, G.A. Gazieva. Cascade of Michael Addition/Retro‐Michael Reaction/Skeletal Rearrangement in the Synthesis of Arylmethylidene Derivatives of Imidazothiazolotriazines. Chemistry Select Vol. 4(35) - P.10483-10487 DOI:10.1002/slct.201902461
  4. Fershtat L.L., Makhova N.N. 1,2,5‐Oxadiazole‐Based High‐Energy‐Density Materials: Synthesis and Performance. ChemPlusChem Vol.85(1)- P.13-42 DOI: 10.1002/cplu.201900542
  5. Zhilin E.S., Bystrov D.M., Ananyev I.V., Fershtat L.L., Makhova N.N. Straightforward Access to the NO‐Donor Azasydnone Scaffold by Cascade Reactions of Amines. Chemistry European Journal Vol.25(63) - P.14284-14289 DOI: 10.1002/chem.201903526
  6. Fedyanin I. V., Lyssenko K.A., Fershtat L. L., Muravyev N.V.,Makhova N.N. Crystal solvates of energetic 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane (HNIW) molecule with [bmim]-based ionic liquids. Crystal Growth & Design 19(7) - P.3660-3669. DOI: 10.1021/acs.cgd.8b01835
  7. Zhilin E.S., Fershtat L.L.,Bystrov D.M.,Kulikov A.S., Dmitrienko A.O.,Ananyev I.V.,Makhova N.N. Renaissance of 1,2,5-Oxadiazolyl Diazonium Salts: Synthesis and Reactivity. European Journal of Organic Chemistry 26 - P.4248-4259. DOI: 10.1002/ejoc.201900622
  8. M.D. Vedenyapina, V.V. Kuznetsov, N.N. Makhova, D. I. Rodikova. Kinetics and Mechanism of the Anodic Dissolution of Gold in a Solution of 1,2-Diaminoethane. Russian Journal of Physical Chemistry 93(3) - P. 466-469. DOI: 10.1134/S0036024419020304
  9. Khaikin L. S.,Kochikov I. V., Rykov, A.N., Grikina O. E., Ageev G. G., Shishkov I. F., Kuznetsov V. V., Makhova N. N. Equilibrium structures of the tetramezine diastereomers and their ratio: joint analysis of gas phase electron diffraction, quantum chemistry, and spectroscopic data. Physical Chemistry Chemical Physics 21(10) P.5598-5613. DOI: 10.1039/C8CP07607C
  10. Larin A.A., Muravyev N. V.,Pivkina A.N., Suponitsky K.Yu.,Ananyev I.V., Khakimov D.V., Fershtat L. L., Makhova N.N. Assembly of Tetrazolylfuroxan Organic Salts: Multipurpose Green Energetic Materials with High Enthalpies of Formation and Excellent Detonation Performance. Chemistry - A European Journal - 25(16) : 4225-4233. DOI: 10.1002/chem.201806378
  11. Marochkin I. I.,Kuznetsov V. V., Rykov A. N., Makhova N. N.,Shishkov I.F. Molecular structure study of 1,2,3-trimethyldiaziridine by means of gas electron diffraction method. Structural Chemistry 30(2) : 457-464. DOI:10.1007/s11224-018-1213-2
  12. Fershtat L. L., Bystrov D. M., Zhilin E. S., Makhova N. N. N-Oxide-Controlled Chemoselective Reduction of Nitrofuroxans. Synthesis-Stuttgart 51(3) : 747-756 DOI:10.1055/s-0037-1611056
  13. Epishina M. A.,Kulikov A.S., Fershtat L. L.,Ananyev I.V., Makhova N. N. Synthesis of new pharmacologically oriented heterocyclic ensembles, [2-(1H-pyrazol-1-yl)thiazol-4-yl]furoxans. Mendeleev Communications - 29(3) : 288-291 DOI:10.1016/j.mencom.2019.05.015
  14. S. A. Pukhov, L. A. Anikina, A. A. Larin, L.L. Fershtat, A. S. Kulikov, N. N Makhova. Hetarylfuroxans: cytotoxic effect and induction of apoptosis in chronic myeloid leukemia K562 cells. Russian Chemical Bulletin 68(1) :158-162. DOI: 10.1007/s11172-019-2431-5
  15. Baranov V. V., Barsegyan Y. A.,Kolotyrkina N. G.,Kravchenko A. N. Highly selective synthesis of tricyclic compounds from semithioglycoluril, formaldehyde and amines. Mendeleev Communications -29 (3) : 323-325 DOI:10.1016/j.mencom.2019.05.028
  16. Baranov V.V., Baganova A. A., Chikunov I. E., Karnoukhova V. A., Kravchenko A. N. Unexpected formation of novel two-component gels comprising of glycoluril carboxylic acid amides and imidazole: Synthesis and morphology. Tetrahedron Letters - 60 (17) : 1174-1178 DOI:10.1016/j.tetlet.2019.03.053
  17. Baranov V.V., Yatsenko E. L., Melnikova E. K., Nelyubina Y. V., Kravchenko A. N. Efficient method for the synthesis of 1,3-unsubstituted 2-imino-5-oxooctahydroimidazo[4,5-d]imidazolium iodides based on thioglycolurils. Chemistry of heterocyclic compounds 55 (2) :160-166 DOI:10.1007/s10593-019-02433-5
  18. Baranov V. V., Antonova M.M.,Kolotyrkina N.G., Zanin I.E., Kravchenko A. N. Direct Synthesis of 1-Alkyl-6-hydroxyalkyl-3a,6a-diphenylglycolurils from 1-Alkylimidazolinones and Their Cyclic Analogues. Synlett - 30(3) : 299-302. DOI:10.1055/s-0037-1611937
  19. Izmest'ev A. N.,Vasileva D.A.,Melnikova E.K., Kolotyrkina N.G.,Borisova I.A., Kravchenko A.N.,Gazieva G.A. Skeletal rearrangement of arylmethylideneimidazo[4,5-e]thiazolo[3,2-b]-1,2,4-triazine-2,7-diones in the synthesis of the corresponding imidazo[4,5-e]thiazolo[2,3-c]-1,2,4-triazine-2,8-diones. New Journal of Chemistry - 43(2) :1038-1052 DOI:10.1039/c8nj05058a
  20. Alexey O. Chagarovskiy, Vladimir V. Kuznetsov, Olga A. Ivanova, Alexander S. Goloveshkin, Irina I. Levina, Nina N. Makhova, Igor V. Trushkov Synthesis of 1-Substituted Pyrazolines by Reaction of Donor-Acceptor Cyclopropanes with 1,5-Diazabicyclo[3.1.0]hexanes European Journal of Organic Chemistry Volume 2019, Issue31-32, Pages 5475-5485 DOI: 10.1002/ejoc.201900579

2018

  1. A.S. Kulikov, M.A. Epishina, A.I. Churakov,L.V. Anikina,L.L. Fershtat, N.N. Makhova. Regioselective synthesis, structural diversification and cytotoxic activity of (thiazol-4-yl)furoxans. Mendeleev Communications 28(6) : 623-625 DOI:10.1016/j.mencom.2018.11.020
  2. A.A. Larin, L.L. Fershtat, N. E. Ustyuzhanina, M.L. Gening,N.E. Nifantiev, N.N. Makhova. New hybrid furoxan structures with antiaggregant activity Mendeleev Communications 28(6):595-597 DOI:10.1016/j.mencom.2018.11.010
  3. I.I. Marochkin, V. V. Kuznetsov, A.N. Rykov, N.N. Makhova, I.F. Shishkov. Molecular structure study of 1,2,3-trimethyldiaziridine by means of gas electron diffraction method. Structural Chemistry 30(3) - 457-464 DOI:10.1007/s11224-018-1213-2
  4. V.V. Kuznetsov, V.V. Kachala, M.M. Makhova. Synthesis of hybrid structures comprising diaziridine and cyclopropane rings in one molecule Mendeleev Communications 28(5):497-500 DOI: 10.1016/j.mencom.2018.09.015
  5. B. V. Lyalin, V.L. Sigacheva, L.L. Fershtat, N.N. Makhova, V.A. Petrosyan. Eco-friendly N–N coupling of aminofuroxans into azofuroxans under the action of electrogenerated hypohalites. Mendeleev Communications 28(5):518-520 DOI:10.1016/j.mencom.2018.09.023
  6. A.S. Kulikov, M.A. Epishina, L.L. Fershtat, N.N. Makhova. Effective synthesis of 7H-1,2,4-triazolo[3,4-b][1,3,4]thiadiazines Chemistry of Heterocyclic Compounds 54(6) DOI:10.1007/s10593-018-2325-8
  7. A.A. Larin, I.V. Ovchinnikov, L.L. Fershtat, N.N. Makhova. 3,3′-(Diazene-1,2-diyl)bis[4-(nitroamino)-1,2,5-oxadiazole 2-oxide] Molbank 2018(3):M1003 DOI:10.3390/M1003
  8. I.V. Trushkov, A.O. Chagarovskiy, V. Vasin, V.V. Kuznetsov, O.A. Ivanova, V.B. Rybakov, A.N. Shumsky, N.N. Makhova. (3+3)‐Annulation of Donor‐Acceptor Cyclopropanes with Diaziridines. Angewandte Chemie 57, 10338 –10342. DOI:10.1002/ange.20180525
  9. D.M. Bystrov, E.S. Zhilin, L.L. Fershtat, A.A. Romanova, I.V. Ananyev, N. N Makhova. Tandem Condensation/Rearrangement Reaction of 2‐Aminohetarene N‐Oxides for the Synthesis of Hetaryl Carbamates. Advanced Synthesis & Catalysis 360 (16), Pages 3157-3163 DOI:10.1002/adsc.201800407
  10. N.N.Makhova, L.L. Fershtat. Recent advances in the synthesis and functionalization of 1,2,5-oxadiazole 2-oxides Tetrahedron Letters 59:2317–2326 DOI:10.1016/j.tetlet.2018.04.070
  11. E.P. Altova, V.V. Kuznetsov, I.I. Marochkin, A.N. Rykov, N.N Makhova, I.F. Shishkov. 3-Cyclopropyl-1,2-dimethyldiaziridine: synthesis and study of molecular structure by gas electron diffraction method. Structural Chemistry 29(3), pages 815–822 DOI:10.1007/s11224-018-1104-6
  12. M.D. Vedenyapina, D.I. Rodikova, V.V. Kuznetsov, N.N Makhova, A.A. Vedenyapin. Anodic corrosion of gold in solutions of diaminoalkanes Mendeleev Communications 28(2):181-183 DOI: 10.1016/j.mencom.2018.03.024
  13. N. E. Ustyuzhanina, L.L. Fershtat, M.L. Gening, N.E. Nifantiev, N.N. Makhova. Antiaggregant activity of water-soluble furoxans Mendeleev Communications 28(1):49-51 DOI: 10.1016/j.mencom.2018.01.016

2017

  1. G. A. Gazieva, T. B. Karpova, T. V. Nechaeva, Y. V. Nelyubina, I. E. Zanin, A. N. Kravchenko. Synthesis of N-{5-Oxo-2-thioxo(2,5-dithioxo)hexahydroimidazo-[4,5-d]imidazol-1(2H)-yl}formamides. Synlett 28(7): 858-862. DOI: 10.1055/s-0036-1588388
  2. Y. A. Barsegyan, V. V. Baranov , A. N. Kravchenko. Glycolurils in the synthesis of fused polyheterocyclic compounds. Chemistry of Heterocyclic Compounds volume 53, p.116–122. DOI: 10.1007/s10593-017-2029-5
  3. V.V. Baranov, M. M. Antonova, V. A. Karnoukhova, A. N. Kravchenko. Unusual formation of imidazooxazolone in the reaction of 1-[(2-Acetylamino)ethyl]imidazoloe with KSCN in the presence of AcOH. Arkivoc (iii):63-72. DOI: 10.3998/ark.5550190.p010.048
  4. L. L. Fershtat, N. N. Makhova. Molecular hybridization tool in development of furoxan-based NO-donor prodrugs. ChemMedChem V.12, Issue 9, Pages 622-638. DOI: 10.1002/cmdc.201700113
  5. V. V.Baranov, M. M. Antonova,V. A. Karnoukhova, A. N. Kravchenko. Unexpected reductive transformation of 1-substituted 5-hydroxy-4,5-diphenyl-1 H -imidazol-2(5 H )-ones and their cyclic analogs by the reaction with thiourea and hydrochloric acid. Tetrahedron Letters Volume 58, Issue 23, Pages 2203-2205. DOI: 10.1016/j.tetlet.2017.04.061
  6. L. L. Fershtat, M. R. Radzhabov, A. A. Romanova, I.V. Ananyev, N. N. Makhova. Lewis acid-catalyzed Wolff cyclocondensation in the synthesis of (1H-1,2,3-triazolyl)furoxans. Arkivoc (iii):140-150. DOI: 10.3998/ark.5550190.p010.070
  7. E. V.Ivanov, E. Yu.Lebedeva, S.G.Petrovskaya,V.V.Baranov,A.N.Kravchenko, N.G.Ivanova. Volume-related interaction parameters for dilute solutions of Mebicaret (2,4-dimethyl-6,8-diethylglycoluril) in normal and heavy water between 278.15 K and 318.15 K. Journal of Molecular Liquids 242, Pages 160-167. DOI: 10.1016/j.molliq.2017.07.003
  8. I. V. Kuchurov, M. N. Zharkov, L. L. Fershtat, N. N. Makhova, S. G. Zlotin. Prospective Symbiosis of Green Chemistry and Energetic Materials. ChemSusChem 10(20) Pages 3914-3946. DOI: 10.1002/cssc.201701053
  9. G. A. Gazieva, S. A. Serkov, N. V. Sigay, N. N. Kostikova, L. D. Popov, A. N. Kravchenko. Functionally substituted aromatic aldehydes as reagents in the synthesis of new substituted thioglycolurils. Arkivoc (iii):279-286. DOI: 10.24820/ark.5550190.p010.243
  10. A. S. Kulikov, A. A. Larin, L. L. Fershtat, L. V.Anikina, S. A. Pukhov, S.G. Klochkov, M. I. Struchkova, A.A. Romanova, I. V. Ananyev, N. N. Makhova. Synthesis, structural characterization and cytotoxic activity of heterocyclic compounds containing the furoxan ring. Arkivoc (iii):250 - 268. DOI: 10.24820/ark.5550190.p010.229
  11. A. A. Larin, L. L. Fershtat, I.V. Ananyev, N. N. Makhova. Versatile approach to heteroarylfuroxan derivatives from oximinofuroxans via a one-pot, nitration/thermolysis/[3+2]-cycloaddition cascade. Tetrahedron Letters 58(42) P. 3993-3997. DOI:10.1016/j.tetlet.2017.09.013
  12. G. A. Gazieva, L.V.Anikina, T.V.Nechaeva, S.A.Pukhov, T. B.Karpova, S.V.Popkov, Y. V.Nelyubina, N.G. Kolotyrkina, A. N.Kravchenko. Synthesis and biological evaluation of new substituted thioglycolurils, their analogues and derivatives. European Journal of Medicinal Chemistry 140. DOI:10.1016/j.ejmech.2017.09.009
  13. A. S. Kulikov, M.A. Epishina, L. L. Fershtat, A. A. Romanova, N. N.Makhova. Effective synthesis of 6-substituted 7 H-tetrazolo[5,1- b][1,3,4]thiadiazines via a one-pot condensation/nitrosation/azide-tetrazole tautomerism reaction sequence. Tetrahedron Letters 58(42) Pages 3998-4002. DOI: 10.1016/j.tetlet.2017.09.014
  14. L. L. Fershtat, I. V. Ovchinnikov, M.A. Epishina , A. A. Romanova, D.B. Lempert , N.V. Muravyev, N.N. Makhova. Assembly of Nitrofurazan and Nitrofuroxan Frameworks for High-Performance Energetic Materials. ChemPlusChem 82(11): 1315-1319. DOI:10.1002/cplu.201700340
  15. I.V. Kuchurov, S.S. Arabadzhi, M.N. Zharkov, L.L. Fershtat, S.G. Zlotin. Sustainable Synthesis of Polynitroesters in the Freon Medium and their in Vitro Evaluation as Potential Nitric Oxide Donors. ACS Sustainable Chemistry & Engineering 6(2) pages 2535–2540. DOI:10.1021/acssuschemeng.7b04029
  16. V.V. Kuznetsov, I.I. Marochkin, A.S. Goloveshkin, N.N. Makhova I.F. Shishkov Comparable study of the structure of 1,2-bis(2-acetamidoethyl) diaziridine and 3,3-diethyldiaziridine with structures of related compounds by X-ray diffraction analysis and quantum chemical calculations Structural Chemistry 28(4) - P.1211–1221 DOI : 10.1007/s11224-016-0908-5

2016

  1. E.V.Ivanov, D.V.Batov, V.V.Baranov, A.N.Kravchenko. Temperature-dependent thermochemical properties of the Mebicaret (2,4-dimethyl-6,8-diethylglycoluril) solutions in H2O and D2O at the ambient pressure. Thermochimica Acta, Volumes 627–629, Pages 48-54 DOI: 10.1016/j.tca.2016.01.010
  2. L.L. Fershtat, A.A. Larin, M.A. Epishina, I.V. Ovchinnikov, A.S. Kulikov, I.V. Ananyev, N.N. Makhova Design of hybrid heterocyclic systems with furoxanylpyridine core via tandem hetero-Diels–Alder/retro-Diels–Alder reactions of (1,2,4-triazin-3-yl)furoxans. RSC Adv.,6, 31526-31539 DOI: 10.1039/C6RA05110C
  3. V. V. Kuznetsov, M. D. Vedenyapina, M. I. Pleshchev, S. B. Gashev, N. N. Makhova, A. A. Vedenyapin Kinetics and mechanism of N-chloromethylamine decomposition in solutions. Russian Journal of Physical Chemistry 90(3):541-544 DOI: 10.1134/S0036024416030225
  4. A.N.Kravchenko, I.E.Chikunov, G.A.Gazieva, N.N.Makhova Efficient synthesis of N,N’-methylenebisglycolurils. Mendeleev Communications 26(2):136–138 DOI: 10.10 16/j.mencom.2016.03.018
  5. G.A. Gazieva, L.V. Anikina, S.A. Pukhov, T.B. Karpova, Y.V. Nelyubina, A.N. Kravchenko Substituted N-aminothioglycolurils containing thiosemicarbazone moiety and their cytotoxic activity in vitro. Molecular Diversity 20(4), p.837–846 DOI: 10.1007/s11030-016-9671-1
  6. L.L.Fershtat, A.A.Larin, M.A.Epishina, A.S.Kulikov, I.V.Ovchinnikov, I.V.Ananyev, N.N.Makhova Regioselective synthesis of bifuroxanyl systems with the 3nitrobifuroxanyl core via a one-pot acylation/nitrosation/cyclization cascade. Tetrahedron Letters 57(38), pages 4268-4272 DOI: 10.1016/j.tetlet.2016.08.011
  7. M. D. Vedenyapina, V. V. Kuznetsov, N. N. Makhova, A. A. Vedenyapin Mechanism of the anodic dissolution of gold in solutions of 6-alkyl-1,5-diazabicyclo[3.1.0]hexanes. Russian Journal of Physical Chemistry 90(9):1903-1908 DOI: 10.1134/S0036024416090284
  8. G. A. Gazieva, T. B. Karpova, T. V. Nechaeva, A. N. Kravchenko Ring contraction of 1,2,4-triazine derivatives in the synthesis of imidazoles. Russian Chemical Bulletin 65(9):2172-2182 DOI: 10.1007/s11172-016-1565-y
  9. Alexei N. Izmest’ev, G.A. Gazieva, N.V. Sigay,S.A. Serkov, V.A. Karnoukhova,V.V. Kachala, A.S. Shashkov,I.E. Zanin,A. N. Kravchenko, N.N. Makhova An effective one-pot access to polynuclear dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties via a 1,3-dipolar cycloaddition strategy. Beilstein Journal of Organic Chemistry 12(1): 2240-2249 DOI: 10.3762/bjoc.12.216
  10. L.L. Fershtat, N.N. Makhova New approaches for the synthesis of non-annulated polynuclear heterocyclic systems incorporating 1,2,5-oxadiazole ring. Russian Chemical Reviews 85(10) - p. 1097 DOI: 10.1070/RCR4619
  11. V. V.Kuznetsov, A.S.Shevtsov, M.I.Pleshchev, Yu.A.Strelenko, N.N.Makhova Diastereoselective synthesis of 1,3-di- and 1,3,3-trisubstituted diaziridines coupled with neurotransmitter amino acids. Mendeleev Communications 26(5)- p.391-394 DOI: 10.1016/j.mencom.2016.09.008
  12. M. D. Vedenyapina, G. Ts. Ubushieva, V. V. Kuznetsov, N. N. Makhova, A. A. Vedenyapin Anodic dissolution of gold in a solution of 1,3-diaminopropane with the formation of a cathodic deposit and a colloidal solution of Au. Russian Journal of Physical Chemistry 90(11):2312-2315 DOI: 10.1134/S0036024416110297
  13. L.L.Fershtat, M.A.Epishina, I.V.Ovchinnikov, M.I.Struchkova, A.A.Romanova, I.V.Ananyev, N.N.Makhovaa Side-chain prototropic tautomerism of 4-hydroxyfuroxans in methylation reactions. Tetrahedron Letters 57(50) - p.5685-5689 DOI: 10.1016/j.tetlet.2016.11.023
  14. N.E.Ustyuzhanina, L.L.Fershtat, M.L.Gening, N.E.Nifantiev, N.N.Makhova New insight into the antiaggregant activity of furoxans. Mendeleev Communications 26(6):513-515 DOI: 10.1016/j.mencom.2016.11.018
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