1. 2017
  2. A novel diastereoselective α-functionalization of proline with benzaldehydes: synthesis of α-(α-hydroxybenzyl)prolines

    Moshkin, V. S., Sosnovskikh, V. Y. & Pavlushin, A. V., 1 Nov 2017, In: Mendeleev Communications. 27, 6, p. 628-630 3 p.

    Research output: Contribution to journalArticlepeer-review

  3. Noncatalytic destruction of 5-acylcomanic acid esters in the presence of 2-methylindoles as a new method for the synthesis of indolylchalcones

    Obydennov, D. L., Sosnovskikh, V. Y. & Pankina, E. O., 1 Aug 2017, In: Chemistry of Heterocyclic Compounds. 53, 8, p. 924-926 3 p.

    Research output: Contribution to journalArticlepeer-review

  4. 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 journalArticlepeer-review

  5. Preparative synthesis of 2,2-dimethyl-5-(trifluoroacetyl)-1,3-dioxane-4,6-dione (2-trifluoroacetyl Meldrum's acid) and 2,2-dimethyl-6-(trifluoromethyl)-4H-1,3-dioxin-4-one and their synthetic usefulness as (trifluoroacetyl)ketene precursors

    Sevenard, D. V., Didenko, A. V., Lorenz, D., Vorobiev, M., Stelten, J., Dülcks, T. & Sosnovskikh, V. Y., 16 Mar 2017, In: Tetrahedron. 73, 11, p. 1495-1502 8 p.

    Research output: Contribution to journalArticlepeer-review

  6. Synthesis of ethyl 4-(isoxazol-4-yl)-2,4-dioxobutanoates from ethyl 5-aroyl-4-pyrone-2-carboxylates and hydroxylamine

    Obydennov, D. L., Khammatova, L. R. & Sosnovskikh, V. Y., 1 Mar 2017, In: Mendeleev Communications. 27, 2, p. 172-174 3 p.

    Research output: Contribution to journalArticlepeer-review

  7. (3+2) Cycloaddition of N-methylazomethine ylide obtained from sarcosine and formaldehyde to CH-and NH-acidic enones and enamides

    Buev, E. M., Moshkin, V. S. & Sosnovskikh, V. Y., Feb 2017, In: Chemistry of Heterocyclic Compounds. 53, 2, p. 167-172 6 p.

    Research output: Contribution to journalArticlepeer-review

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