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  1. 2019

  2. 3-Nitro-2H-chromenes in [3+2] cycloaddition reaction with azomethine ylides derived from N-unsubstituted α-amino acids and isatins: regio- and stereoselective synthesis of spirochromeno[3,4-c]pyrrolidines

    Kutyashev, I. B., Barkov, A. Y., Korotaev, V. Y. & Sosnovskikh, V. Y., 15 Jun 2019, In: Chemistry of Heterocyclic Compounds. 55, 6, p. 529-540 12 p.

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

  3. A regio- And stereocontrolled approach to the synthesis of 4-CF3-substituted spiro[chromeno[3,4-C] pyrrolidine-oxindoles] via reversible [3+2] cycloaddition of azomethine ylides generated from isatins and sarcosine to 3-nitro-2-(trifluoromethyl)-2 H -chromenes

    Kutyashev, I. B., Ulitko, M. V., Barkov, A. Y., Zimnitskiy, N. S., Korotaev, V. Y. & Sosnovskikh, V. Y., 1 Jan 2019, In: New Journal of Chemistry. 43, 47, p. 18495-18504 10 p.

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

  4. ПОСЛЕДНИЕ ДОСТИЖЕНИЯ В ХИМИИ 3-НИТРО-2Н- И 3-НИТРО-4Н-ХРОМЕНОВ

    Korotaev, V. Y., Kutyashev, I. B., Barkov, A. Y. & Sosnovskikh, V. Y., 1 Jan 2019, In: Russian Chemical Reviews. 88, 1, p. 27-58 32 p.

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

  5. 2018

  6. Stabilized azomethine ylides derived from indeno[1,2-b]quinoxalinones in [3+2] cycloaddition reactions with electrophilic alkenes

    Korotaev, V. Y., Zimnitskiy, N. S., Barkov, A. Y., Kutyashev, I. B. & Sosnovskikh, V. Y., 1 Oct 2018, In: Chemistry of Heterocyclic Compounds. 54, 10, p. 905-922 18 p.

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

  7. Reactions of 3,3,3-Trihalogeno-1-nitropropenes with Arenes in the Superacid CF3SO3H: Synthesis of (Z)-3,3,3-Trihalogeno-1,2-diarylpropan-1-one Oximes and Study on the Reaction Mechanism

    Golushko, A. A., Sandzhieva, M. A., Ivanov, A. Y., Boyarskaya, I. A., Khoroshilova, O. V., Barkov, A. Y. & Vasilyev, A. V., 7 Sept 2018, In: Journal of Organic Chemistry. 83, 17, p. 10142-10157 16 p.

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

  8. 3-Nitro-2-phenyl-2-(trifluoromethyl)-2H-chromenes in reaction with N-methylazomethine ylide: stereoselective synthesis of 3a,4,4-trisubstituted chromeno[3,4-c]pyrrolidines

    Korotaev, V. Y., Kutyashev, I. B., Barkov, A. Y. & Sosnovskikh, V. Y., 1 Sept 2018, In: Chemistry of Heterocyclic Compounds. 54, 9, p. 852-858 7 p.

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

  9. Unexpected regiochemistry in [3+2] cycloaddition reaction of azomethine ylides of indenoquinoxalinone series to arylidene malononitriles

    Barkov, A. Y., Zimnitskiy, N. S., Kutyashev, I. B., Korotaev, V. Y. & Sosnovskikh, V. Y., 1 Jan 2018, In: Chemistry of Heterocyclic Compounds. 54, 1, p. 43-50 8 p.

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

  10. 2017

  11. Highly regio- and stereoselective 1,3-dipolar cycloaddition of stabilised azomethine ylides to 3,3,3-trihalogeno-1-nitropropenes: Synthesis of trihalomethylated spiroindenepyrroli(zi)dines

    Barkov, A. Y., Zimnitskiy, N. S., Kutyashev, I. B., Korotaev, V. Y., Moshkin, V. S. & Sosnovskikh, V. Y., 1 Dec 2017, In: Journal of Fluorine Chemistry. 204, p. 37-44 8 p.

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

  12. Regio- and stereoselective 1,3-dipolar cycloaddition reactions between arylideneacetones and stabilized azomethine ylides obtained from ninhydrin and indenoquinoxalinones

    Barkov, A. Y., Zimnitskiy, N. S., Kutyashev, I. B., Korotaev, V. Y. & Sosnovskikh, V. Y., Dec 2017, In: Chemistry of Heterocyclic Compounds. 53, 12, p. 1315-1323 9 p.

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

  13. 2-Substituted 3-nitro-2H-chromenes in reaction with azomethine ylide derived from ninhydrin and proline: regio- and stereoselective synthesis of spiro[chromeno[3,4-a]pyrrolizidine-11,2'-indene]-1',3'-diones

    Korotaev, V. Y., Kutyashev, I. B., Barkov, A. Y. & Sosnovskikh, V. Y., Nov 2017, In: Chemistry of Heterocyclic Compounds. 53, 11, p. 1192-1198 7 p.

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

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