1. 2022
  2. One-Pot Synthesis of Multifunctionalized 1-Pyrrolines from 2-Alkyl-2 H-azirines and Diazocarbonyl Compounds

    Filippov, I. P., Novikov, M. S., Khlebnikov, A. F. & Rostovskii, N. V., 22 Jun 2022, In: Journal of Organic Chemistry. 87, 13, p. 8835-8840 6 p.

    Research output: Contribution to journalArticlepeer-review

  3. Synthesis of Imidazo[1,2- a]pyridines via Near UV Light-Induced Cyclization of Azirinylpyridinium Salts

    Filippov, I. P., Agafonova, A. V., Titov, G. D., Smetanin, I. A., Rostovskii, N. V., Khlebnikov, A. F. & Novikov, M. S., 27 Apr 2022, In: Journal of Organic Chemistry. 87, 9, p. 6514-6519 6 p.

    Research output: Contribution to journalArticlepeer-review

  4. 2021
  5. Rhodium-Catalyzed Synthesis of 2-Aroylpyrimidines via Cascade Heteropolyene Rearrangement

    Tiuftiakov, N. Y., Strelnikova, J. O., Filippov, I. P., Khaidarov, A. R., Khlebnikov, A. F., Bunev, A. S., Novikov, M. S. & Rostovskii, N. V., 23 Aug 2021, In: Organic Letters. 23, 17, p. 6998-7002 5 p.

    Research output: Contribution to journalArticlepeer-review

  6. 2020
  7. Recent Advances in Denitrogenative Reactions of Pyridotriazoles

    Filippov, I. P., Titov, G. D. & Rostovskii, N. V., 1 Dec 2020, In: Synthesis (Germany). 52, 23, p. 3564-3576 13 p.

    Research output: Contribution to journalReview articlepeer-review

  8. 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

    Filippov, I. P., Novikov, M. S., Khlebnikov, A. F. & Rostovskii, N. V., 22 May 2020, In: European Journal of Organic Chemistry. 2020, 19, p. 2904-2913 10 p.

    Research output: Contribution to journalArticlepeer-review

  9. 2018
  10. A novel approach to 5H-pyrazino[2,3- b] indoles via annulation of 3-diazoindolin-2-imines with 2H-azirines or 5-alkoxyisoxazoles under Rh(II) catalysis

    Ruvinskaya, J. O., Rostovskii, N. V., Filippov, I. P., Khlebnikov, A. F. & Novikov, M. S., 7 Jan 2018, In: Organic and Biomolecular Chemistry. 16, 1, p. 38-42 5 p.

    Research output: Contribution to journalArticlepeer-review

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