1. 2013
  2. An improved synthesis and some reactions of diethyl 4-oxo-4H-pyran-2,5-dicarboxylate

    Obydennov, D. L., Roeschenthaler, G-V. & Sosnovskikh, V. Y., 27 Nov 2013, In: Tetrahedron Letters. 54, 48, p. 6545-6548 4 p.

    Research output: Contribution to journalArticlepeer-review

  3. A simple two-step synthesis of 2-(alkylamino)-1-arylethanols, including racemic adrenaline, from aromatic aldehydes via 5-aryloxazolidines

    Moshkin, V. S. & Sosnovskikh, V. Y., 30 Oct 2013, In: Tetrahedron Letters. 54, 44, p. 5869-5872 4 p.

    Research output: Contribution to journalArticlepeer-review

  4. Synthesis and reactivity of 5-polyfluoroalkyl-5-deazaalloxazines

    Dudkin, S., Iaroshenko, V. O., Sosnovskikh, V. Y., Tolmachev, A. A., Villinger, A. & Langer, P., 28 Aug 2013, In: Organic and Biomolecular Chemistry. 11, 32, p. 5351-5361 11 p.

    Research output: Contribution to journalArticlepeer-review

  5. Synthesis of beta-(trifluoromethyl)furans and spiro-gem-dichlorocyclopropanes from cyclic 1,3-dicarbonyl compounds and alpha-(trihaloethylidene)nitroethanes

    Barkov, A. Y., Korotaev, V. Y. & Sosnovskikh, V. Y., 7 Aug 2013, In: Tetrahedron Letters. 54, 32, p. 4181-4184 4 p.

    Research output: Contribution to journalArticlepeer-review

  6. Sulfur analogs of fluorinated pyrones, chromones and coumarins

    Sosnovskikh, V. Y., 1 Aug 2013, In: Journal of Sulfur Chemistry. 34, 4, p. 432-443 12 p.

    Research output: Contribution to journalLiterature reviewpeer-review

  7. Synthesis of benzopyranopyrrolidines via 1,3-dipolar cycloaddition of nonstabilized azomethine ylides with 3-substituted coumarins

    Moshkin, V. S., Sosnovskikh, V. Y. & Roeschenthaler, G-V., 22 Jul 2013, In: Tetrahedron. 69, 29, p. 5884-5892 9 p.

    Research output: Contribution to journalArticlepeer-review

  8. A novel, two-step synthesis of 4-pyridone-3-carboxamides from 2-cyano-4-pyrones

    Obydennov, D. L., Sidorova, E. S., Usachev, B. I. & Sosnovskikh, V. Y., 12 Jun 2013, In: Tetrahedron Letters. 54, 24, p. 3085-3087 3 p.

    Research output: Contribution to journalArticlepeer-review

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