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  1. 2017

  2. Highly diastereoselective synthesis of novel 2,3,4-trisubstituted chromanes via the reaction of 3-nitro-2-(trihalomethyl)- and 3-nitro-2-phenyl-2H-chromenes with 1-morpholinocyclopentene

    Korotaev, V. Y., Kutyashev, I. B., Barkov, A. Y. & Sosnovskikh, V. Y., 24 Aug 2017, In: Tetrahedron. 73, 34, p. 5122-5137 16 p.

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

  3. 3-Nitro-2-(trihalomethyl)-2H-chromenes in reactions with sodium azide: synthesis of 4-(trihalomethyl)-2,4-dihydrochromeno[3,4-d][1,2,3]triazoles

    Korotaev, V. Y., Kutyashev, I. B., Barkov, A. Y. & Sosnovskikh, V. Y., May 2017, In: Chemistry of Heterocyclic Compounds. 53, 5, p. 597-603 7 p.

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

  4. Regio- and stereoselective 1,3-dipolar cycloaddition of indenoquinoxalinone azomethine ylides to beta-nitrostyrenes: synthesis of spiro[indeno[1,2-b]quinoxaline-11,3 '-pyrrolizidines] and spiro[indeno[1,2-b]quinoxaline-11,2 '-pyrrolidines]

    Barkov, A. Y., Zimnitskiy, N. S., Korotaev, V. Y., Kutyashev, I. B., Moshkin, V. S. & Sosnovskikh, V. Y., Apr 2017, In: Chemistry of Heterocyclic Compounds. 53, 4, p. 451-459 9 p.

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

  5. 2016

  6. Highly regio- and stereoselective 1,3-dipolar cycloaddition of stabilised azomethine ylides to 3,3,3-trihalogeno-1-nitropropenes: synthesis of trihalomethylated spiro[indoline-3,2′-pyrrolidin]-2-ones and spiro[indoline-3,3′-pyrrolizin]-2-ones

    Barkov, A. Y., Zimnitskiy, N. S., Korotaev, V. Y., Kutyashev, I. B., Moshkin, V. S. & Sosnovskikh, V. Y., 27 Oct 2016, In: Tetrahedron. 72, 43, p. 6825-6836 12 p.

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

  7. Synthesis of polyfunctionalized benzophenones via the reaction of 3-formylchromones with tertiary push-pull enamines

    Barkov, A. Y., Korotaev, V. Y., Kutyashev, I. B. & Sosnovskikh, V. Y., 21 Apr 2016, In: Tetrahedron. 72, 16, p. 2026-2033 8 p.

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

  8. Uncatalyzed, highly stereoselective addition of alpha-morpholinostyrene to 3-nitro-2-(trihalomethyl)-2H-chromenes. Synthesis of trans cis- and trans-trans-3-nitro-4-phenacyl-(2-trihalomethyl)chromanes

    Korotaev, V. Y., Kotovich, I. V., Barkov, A. Y., Kutyashev, I. B., Kodess, M. I. & Sosnovskikh, V. Y., 7 Jan 2016, In: Tetrahedron. 72, 1, p. 216-226 11 p.

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

  9. 3-Nitro-2-phenyl-2-(trifluoromethyl)-2H-chromenes: synthesis and reactions with nucleophiles

    Barkov, A. Y., Korotaev, V. Y., Kotovich, I. V., Zimnitskiy, N. S., Kutyashev, I. B. & Sosnovskikh, V. Y., 1 Jan 2016, In: Chemistry of Heterocyclic Compounds. 52, 10, p. 814-822 9 p.

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

  10. One-pot synthesis of functionalized benzo[: C] coumarins and their precursors via the reaction of 2-(polyfluoroalkyl)chromones with 4-alkyl-3-cyanocoumarins

    Sosnovskikh, V. Y., Korotaev, V. Y., Kutyashev, I. B., Barkov, A. Y. & Safrygin, A. V., 2016, In: RSC Advances. 6, 63, p. 58188-58202 15 p.

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

  11. 2015

  12. Products from the addition of acetoacetic ester or acetylacetone to 3-nitro-2H-chromenes - axially chiral trans,trans-2,3,4-trisubstituted chromans and related pyrazoles

    Korotaev, V. Y., Kutyashev, I. B., Barkov, A. Y., Ezhikova, M. A., Kodess, M. I. & Sosnovskikh, V. Y., Aug 2015, In: Chemistry of Heterocyclic Compounds. 51, 8, p. 704-708 5 p.

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

  13. Synthesis of trans,trans-2,3,4-trisubstituted chromans from 3-nitro-2De-chromenes and enamines of acetoacetic ester and acetylacetone. A new type of configurationally stable atropisomers

    Korotaev, V. Y., Barkov, A. Y., Ezhikova, M. A., Kodess, M. I. & Sosnovskikh, V. Y., Jun 2015, In: Chemistry of Heterocyclic Compounds. 51, 6, p. 531-540 10 p.

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

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