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  1. 1,2,4-Triazino[5,6,1-i,j]quinolines: a new type of tricyclic analogs of fluoroquinolones

    Lipunova, GN., Nosova, EV., Mochul'skaya, NN., Andreiko, AA., Chasovskikh, OM. & Charushin, VN., Apr 2002, In: Russian Chemical Bulletin. 51, 4, p. 663-667 5 p.

    Research output: Contribution to journal › Article › peer-review

  2. 1,3,4-Oxa(thia)diazino [i,j]-annelated quinolines: A new type of key intermediate in the synthesis of tricyclic fluoroquinolones

    Lipunova, G. N., Nosova, E. V., Charushin, V. N., Sidorova, L. P. & Chasovskikh, O. M., 1 Jan 1998, In: Mendeleev Communications. 8, 4, p. 131-132 2 p.

    Research output: Contribution to journal › Article › peer-review

  3. 1,3,7-Triazapyrene-Based ortho-Carborane Fluorophores: Convenient Synthesis, Theoretical Studies, and Aggregation-Induced Emission Properties

    Smyshliaeva, L. A., Varaksin, M. V., Fomina, E. I., Medvedeva, M. V., Svalova, T. S., Kozitsina, A. N., Demidov, O. P., Borovlev, I. V., Mensch, C., Mampuys, P., Maes, B. U. W., Charushin, V. N. & Chupakhin, O. N., 23 Aug 2021, In: Organometallics. 40, 16, p. 2792-2807 16 p.

    Research output: Contribution to journal › Article › peer-review

  4. 1-Alkyl-1,2,4-triazinium Ylides as 1,3-Dipoles in a Cycloaddition Reaction with Diethyl Acetylenedicarboxylate

    Chupakhin, O. N., Rudakov, B. V., Alexeev, S. G., Shorshnev, S. V. & Charushin, V. N., 1 Jan 1992, In: Mendeleev Communications. 2, 3, p. 85-86 2 p.

    Research output: Contribution to journal › Article › peer-review

  5. 1-Nicotinoylbenzotriazole: A Convenient Tool for Site-Selective Protection of 5,7-Dihydroxycoumarins

    Fatykhov, R. F., Khalymbadzha, I. A., Chupakhin, O. N., Charushin, V. N., Inyutina, A. K., Slepukhin, P. A. & Kartsev, V. G., 1 Jan 2019, In: Synthesis (Germany). 51, 19, p. 3617-3624 8 p.

    Research output: Contribution to journal › Article › peer-review

  6. 2-(5-нитронилфуран-2-ил)-5-метил-6-нитро-1,2,4-триазоло[1,5-а]пиримидин-7(4н)-он и его соли: патент на изобретение

    Чупахин, О. Н., Чарушин, В. Н., Русинов, В. Л., Саватеев, К. В., Уломский, Е. Н., Федотов, В. В., Петров, В. И., Спасов, А. А., Бабкова, В. А. & Бабков, Д. А., 16 Mar 2020, IPC No. C07D 487/04, A61K 31/519, A61P 9/10, A61P 9/04, A61P 3/10, Федеральный институт промышленной собственности, Patent No. 2716715, 30 Jul 2018, Priority No. 2018127985

    Research output: Patent

  7. 2-amino-5-aryl- and 2-amino-5-hetaryl-3-cyano-6-(2-thienyl)pyridines as organic dyes for dye-sensitized solar cells: Synthesis, quantum-chemical calculations, spectral and electrochemical properties

    Verbitskiy, E. V., Slepukhin, P. A., Subbotina, Y. O., Valova, M. S., Schepochkin, A. V., Cheprakova, E. M., Rusinov, G. L. & Charushin, V. N., Sept 2014, In: Chemistry of Heterocyclic Compounds. 50, 6, p. 814-827 14 p.

    Research output: Contribution to journal › Article › peer-review

  8. 2-Aminooxazoles as novel dienophiles in the inverse demand Diels–Alder reaction with 1,2,4-triazines

    Krinochkin, A. P., Mallikarjuna Reddy, G., Kopchuk, D. S., Slepukhin, P. A., Shtaitz, Y. K., Khalymbadzha, I. A., Kovalev, I. S., Kim, G. A., Ganebnykh, I. N., Zyryanov, G. V., Chupakhin, O. N. & Charushin, V. N., 1 Jul 2021, In: Mendeleev Communications. 31, 4, p. 542-544 3 p.

    Research output: Contribution to journal › Article › peer-review

  9. 2-Azaanthracene (microreview) [InlineMediaObject not available see fulltext.]

    Taniya, O. S., Kopchuk, D. S., Khasanov, A. F., Kovalev, I. S., Zyryanov, G. V., Charushin, V. N. & Chupakhin, O. N., 15 Jun 2019, In: Chemistry of Heterocyclic Compounds. 55, 6, p. 505-507 3 p.

    Research output: Contribution to journal › Article › peer-review

  10. 2-Azaanthracenes: A chronology of synthetic approaches and bright prospects for practical applications

    Taniya, O. S., Kopchuk, D. S., Khasanov, A. F., Kovalev, I. S., Santra, S., Rahman, M., Zyryanov, G. V., Majee, A., Charushin, V. N. & Chupakhin, O. N., 1 Jan 2019, In: New Journal of Chemistry. 43, 28, p. 11382-11390 9 p.

    Research output: Contribution to journal › Review article › peer-review

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