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  1. 2022

  2. Homophthalic Monoesters: A New Type of Reagents for the Castagnoli‐Cushman Reaction: A New Type of Reagents for the Castagnoli-Cushman Reaction

    Guranova, N., Bakulina, O., Dar'in, D., Kantin, G. & Krasavin, M., 7 Mar 2022, In: European Journal of Organic Chemistry. 2022, 9, e202101281.

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

  3. Castagnoli-Cushman Reaction of 3-Aryl Glutaric Acids: A Convenient, Diastereoselective Reaction for 6-Oxo-2,4-diarylpiperidine-3-carboxylic Acid Scaffold

    Paramonova, P., Bakulina, O., Nabiyev, A., Dar'in, D. & Krasavin, M., 21 Jan 2022, In: ChemistrySelect. 7, 3, 5 p., e202104011.

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

  4. Synthesis of γ-Sultam-Annelated δ-Lactams via the Castagnoli-Cushman Reaction of Sultam-Based Dicarboxylic Acids

    Firsov, A., Bakulina, O., Dar'In, D., Sokolov, V. V. & Krasavin, M., 21 Jan 2022, In: Journal of Organic Chemistry. 87, 2, p. 1537–1540 4 p.

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

  5. In situ generation of imines by the Staudinger/aza-Wittig tandem reaction combined with thermally induced Wolff rearrangement for one-pot three-component β-lactam synthesis

    Paramonova, P., Lebedev, R., Bakulina, O., Dar'in, D. & Krasavin, M., 2022, In: Organic and Biomolecular Chemistry. 20, p. 9679-9683

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

  6. One-pot sequence of Staudinger/aza-Wittig/Castagnoli-Cushman reactions provides facile access to novel natural-like polycyclic ring system

    Лебедев, Р. Е., Дарьин, Д. В., Кантин, Г. П., Бакулина, О. Ю. & Красавин, М. Ю., 2022, In: Molecules. 27, 23, 8130.

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

  7. КОМБИНАЦИЯ ШТАУДИНГЕР/АЗА-ВИТТИГ КАК МЕТОД ПОЛУЧЕНИЯ ИМИНОВ IN SITU И ИХ ПРИМЕНЕНИЕ В МУЛЬТИКОМПОНЕНТНЫХ РЕАКЦИЯХ

    Парамонова, П. С., Лебедев, Р. Е., Елисеев, И., Бакулина, О. Ю., Дарьин, Д. В. & Красавин, М. Ю., 2022, VI Международная конференция «Современные синтетические методологии для создания лекарственных препаратов и функциональных материалов» (MOSM 2022): сборник тезисов. III-33

    Research output: Chapter in Book/Report/Conference proceeding › Conference abstracts › Research › peer-review

  8. СИНТЕЗ НОВЫХ ИНГИБИТОРОВ КАРБОАНГИДРАЗЫ ЧЕЛОВЕКА НА ОСНОВЕ РЕАКЦИИ КАСТАНЬОЛИ-КУШМАНА

    Парамонова, П. С., Бакулина, О. Ю., Калинин, С. А. & Шаройко, В. В., 2022.

    Research output: Contribution to conference › Abstract › peer-review

  9. 2021

  10. Catalyst-Free Synthesis of Diastereomerically Pure 3-Cyanoazetidin-2-ones via Thermally Promoted Tandem Wolff Rearrangement–Staudinger [2+2] Cycloaddition

    Levashova, E., Bakulina, O., Dar'in, D. & Krasavin, M., 20 Dec 2021, In: ChemistrySelect. 6, 47, p. 13582-13588

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

  11. Facile entry into the 1H-pyrrolo[3,4-b]indolizine-1,3(2H)-dione scaffold via intramolecular Rh(II) carbene trapping

    Chupakhin, E., Bakulina, O., Dar'in, D. & Krasavin, M., 23 Nov 2021, In: Tetrahedron Letters. 85, 3 p., 153467.

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

  12. Synthesis of Diastereomerically Pure 3-Cyanoazetidin-2-ones via Thermally Promoted Tandem Wolff Rearrangement–Staudinger [2+2] Cycloaddition

    Levashova, E. & Bakulina, O. Y., 9 Nov 2021, International Student Conference “Science and Progress”: conference abstracts. СПб: ООО "Сборка", p. 36 1 p.

    Research output: Chapter in Book/Report/Conference proceeding › Conference abstracts › Research

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