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  1. 1,3,5-Triazinanes as Formaldimine Surrogates in the Ugi Reaction

    Golubev, P., Guranova, N. & Krasavin, M., 9 Aug 2020, In: European Journal of Organic Chemistry. 2020, 29, p. 4517-4520 4 p.

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

  2. 1,3,5-ТРИАЗИНАНЫ В РЕАКЦИИ УГИ

    Голубев, П. Р., 2021, p. 112. 1 p.

    Research output: Contribution to conference › Paper

  3. 1-Ethoxypentenynones in synthesis of heterocycles

    Golubev, P. R. & Pankova, A. S., 2015, p. 60.

    Research output: Contribution to conference › Abstract

  4. Brønsted acid mediated cyclizations of ortho aryl(ethynyl)pyrimidines

    Кузнецов, М. А., Шестаков, А. Н., Панькова, А. С., Хлебников, А. Ф. & Голубев, П. Р., 2017, In: Tetrahedron. 73, 27-28, p. 3939-3948

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

  5. Efficient Conversion of Alkenynones to 2-Methylenedihydropyrrolones

    Golubev, P. R. & Pankova, A. S., 2014, p. 153.

    Research output: Contribution to conference › Abstract

  6. Indoline-Based Constrained Peptidomimetic Motifs Obtained via the Joullié–Ugi Reaction of Indolenines.

    Golubev, P., Bakulina, O., Dar'in, D. & Krasavin, M., 2016, In: European Journal of Organic Chemistry. p. 3969-3976

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

  7. “Isocyanide-less” Ugi/Intramolecular Diels-Alder reaction of 5-hydroxymethylfurfural

    Golubev, P., Pankova, A. & Krasavin, M., 13 Jun 2019, In: Tetrahedron Letters. 60, 24, p. 1578-1581 4 p.

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

  8. N-Boc-α-diazo glutarimide as efficient reagent for assembling N-heterocycle-glutarimide diads via Rh(II)-catalyzed N–H insertion reaction

    Кантин, Г. П., Голубев, П. Р., Сапегин, А. В., Бунев, А. С. & Дарьин, Д. В., 7 Dec 2023, In: Beilstein Journal of Organic Chemistry. 19, 19, p. 1841–1848 8 p.

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

  9. New ways to functionalized five-membered nitrogen heterocycles

    Kuznetsov, M. A., Pankova, A. S. & Golubev, P. R., 2015, p. 7.

    Research output: Contribution to conference › Abstract

  10. N-Isocyanodialkylamines generated in situ for the Joullié–Ugi reaction with indolenines

    Golubev, P. & Krasavin, M., 26 Sep 2018, In: Tetrahedron Letters. 59, 39, p. 3532-3536 5 p.

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

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