1. 2016
  2. Transition-Metal-Free Cross-Dehydrogenative Coupling of Triazines with 5,7-Dihydroxycoumarins

    Khalymbadzha, I. A., Chupakhin, O. N., Fatykhov, R. F., Charushin, V. N., Schepochkin, A. V. & Kartsev, V. G., 14 Nov 2016, In: Synlett. 27, 18, p. 2606-2610 5 p., st-2016-d0398-l.

    Research output: Contribution to journalArticlepeer-review

  3. 2017
  4. СИНТЕЗ И ИССЛЕДОВАНИЕ МЕТОДОМ ХРОМАТОМАСС-СПЕКТРОМЕТРИИ 2-АЛКЕНИЛ(ПРОПАРГИЛ)ТИО-4,6-ДИМЕТИЛПИРИМИДИНА

    Шалькова, Е. Н., Ким, Д. Г., Фролова, Т. В. & Фатыхов, Р. Ф., 2017, In: Вестник Южно-Уральского государственного университета. Серия: Химия. 9, 3, p. 19-25 7 p.

    Research output: Contribution to journalArticlepeer-review

  5. 2018
  6. Transition-Metal-Free C-C Coupling of 5,7-Dihydroxybenzopyrones with Quinoxalones and Pteridinones

    Khalymbadzha, I. A., Fatykhov, R. F., Chupakhin, O. N., Charushin, V. N., Tseitler, T. A., Sharapov, A. D., Inytina, A. K. & Kartsev, V. G., 15 Jun 2018, In: Synthesis (Germany). 50, 12, p. 2423-2431 9 p.

    Research output: Contribution to journalArticlepeer-review

  7. 2019
  8. 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 journalArticlepeer-review

  9. New approach to the synthesis of biologically active derivatives of pyranocoumarins

    Inyutina, A. K., Fatykhov, R. F., Khalymbadzha, I. A., Sharapov, A. D., Bobkina, M. V. & Chupakhin, O. N., 11 Jan 2019, Modern Synthetic Methodologies for Creating Drugs and Functional Materials, MOSM 2018: Proceedings of the II International. Santra, S., Zyryanov, G. V. & Sadieva, L. K. (eds.). American Institute of Physics Inc., Vol. 2063. 4 p. 040019. (AIP Conference Proceedings; vol. 2063).

    Research output: Chapter in Book/Report/Conference proceedingConference contributionpeer-review

  10. Optimization of pyran ring annulation in the synthesis of acronycine and its derivatives

    Fatykhov, R. F., Inyutina, A. K., Khalymbadzha, I. A., Sharapov, A. D., Bobkina, M. V. & Chupakhin, O. N., 11 Jan 2019, Modern Synthetic Methodologies for Creating Drugs and Functional Materials, MOSM 2018: Proceedings of the II International. Santra, S., Zyryanov, G. V. & Sadieva, L. K. (eds.). American Institute of Physics Inc., Vol. 2063. 4 p. 040014. (AIP Conference Proceedings; vol. 2063).

    Research output: Chapter in Book/Report/Conference proceedingConference contributionpeer-review

  11. Synthesis of azaheterocyclic derivatives of 5,7-dimethoxycoumarins by CH/CH functionalization with quinazolines

    Sharapov, A. D., Fatykhov, R. F., Bobkina, M. V., Inyutina, A. K., Khalymbadzha, I. A. & Chupakhin, O. N., 11 Jan 2019, Modern Synthetic Methodologies for Creating Drugs and Functional Materials, MOSM 2018: Proceedings of the II International. Santra, S., Zyryanov, G. V. & Sadieva, L. K. (eds.). American Institute of Physics Inc., Vol. 2063. 4 p. 040049. (AIP Conference Proceedings; vol. 2063).

    Research output: Chapter in Book/Report/Conference proceedingConference contributionpeer-review

  12. Functionalization of Aromatic N-Heterocycles via C(sp2)–H/C(sp2)–H CDC Reactions

    Khalymbadzha, I. A., Fatykhov, R. F. & Chupakhin, O. N., 24 Aug 2019, Heterocycles via Cross Dehydrogenative Coupling: Synthesis and Functionalization. Srivastava, A. & Jana, C. K. (eds.). Springer Singapore, p. 35-75 Chapter 2

    Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

  13. Functionalization of Aromatic N-Heterocycles with C(sp3)–H Sources via CDC Reactions

    Fatykhov, R. F., Khalymbadzha, I. A. & Chupakhin, O. N., 24 Aug 2019, Heterocycles via Cross Dehydrogenative Coupling: Synthesis and Functionalization. Srivastava, A. & Jana, C. K. (eds.). Springer Singapore, p. 1-33 33 p. Chapter 1

    Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

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