RUS  ENG
Full version
PEOPLE

Schmidt Elena Yur'evna

Publications in Math-Net.Ru

  1. Base-mediated C-vinylation of ketones with alkynes: synthesis of β,γ-ethylenic ketones and their synthetic applications

    Usp. Khim., 95:1 (2026),  1–21
  2. Acetylene-driven superbase-mediated self-organization of (het)arylpyridines from (het)aromatic nitriles

    Mendeleev Commun., 35:6 (2025),  636–638
  3. Reaction of benzonitriles with acetylene in the KOBut/DMSO/THF system: self-organization of 2-aryl-3-ethynyl-4-aroyl-5-methylpyrroles and aminoacroleins

    Mendeleev Commun., 34:6 (2024),  868–870
  4. The reaction of acetylenes with aldazines in the NaOBut/DMSO system: a contribution to the pyrazole chemistry

    Mendeleev Commun., 34:1 (2024),  110–112
  5. Reaction of acetylenic carbanions with C=N bond: dynamics of development, synthetic divergence, environmental safety

    Usp. Khim., 93:10 (2024),  1–15
  6. Aza-Favorsky reaction with regioisomeric C- and N-linked 1,4-bis(imino)benzenes: Synthetic and reactivity dissimilarities

    Mendeleev Commun., 33:5 (2023),  642–644
  7. Acetylene-driven multi-molecular assemblies of high complexity: imidazo[1,2-a]pyridines and 5-chloro-N-[2-(imidazo[1,2-a]pyridin-6-yl)vinyl]pyridin-2-amine

    Mendeleev Commun., 33:2 (2023),  164–166
  8. Diversifying the superbase-catalyzed C=N bond ethynylation: triaryl-1-pyrrolines and triaryl-1H-pyrroles from N-benzyl aldimines and arylacetylenes

    Mendeleev Commun., 33:1 (2023),  24–26
  9. Multimolecular self-organization of acetylene and arylamines into 1-aryl-3-ethyl-4-vinylpyrroles in the KOBut/DMSO system

    Mendeleev Commun., 30:3 (2020),  315–317
  10. Superbase-promoted multi-molecular acetylene/arylamine self-organization to 1-arylpyrroles

    Mendeleev Commun., 30:1 (2020),  109–111
  11. Quantum chemical comparison of ethynylation and C-vinylation routes in superbase catalyzed reaction of acetylenes with imines

    Mendeleev Commun., 29:6 (2019),  622–624
  12. Diastereoselective synthesis of 5-hydroxy-3-methylalkane-1,6-diones from ketones and acetylene in two atom-economic steps

    Mendeleev Commun., 29:1 (2019),  17–18
  13. Unfolding the frontalin chemistry: a facile selective hydrogenation of 7-methylidene-6,8-dioxabicyclo[3.2.1]octanes, 2:2 ensembles of ketones and acetylene

    Mendeleev Commun., 28:5 (2018),  513–514
  14. 2,4,6-Trisubstituted 3,4-dihydropyrans from acetylene and ketones: deacetylation in the KOBut/DMSO system

    Mendeleev Commun., 28:2 (2018),  145–146
  15. Dioximes of 1,6-heptanediones from acetylene and ketones: only three atom-economic steps

    Mendeleev Commun., 28:2 (2018),  143–144
  16. Acetylene as driving and organizing molecule in the assembling reactions with chalcones in the NaOBut/DMSO superbase system

    Mendeleev Commun., 28:1 (2018),  47–48
  17. 2-Aminopyrimidines in just two steps from ketones, acetylenes and guanidine via β,γ enones

    Mendeleev Commun., 27:3 (2017),  283–284
  18. Base-catalyzed cascade dimerization of γ-aryl-β,γ-enones into acylated terphenyls

    Mendeleev Commun., 26:5 (2016),  378–379
  19. Base-catalyzed α-vinylation of ketones with acetylenes as a key step in one-pot synthesis of pyrazolines and pyrazoles

    Mendeleev Commun., 25:2 (2015),  131–132
  20. Reaction of (het)aryl cyclohexyl ketoximes with acetylene in the two-phase KOH/DMSO/n-hexane system: en route to spirocyclic 3H-pyrroles

    Mendeleev Commun., 25:2 (2015),  129–130
  21. Domino assembly of functionalized cyclopentenols from 1,5-diphenylpentane-1,5-dione and phenylacetylene in the KOH/DMSO suspension

    Mendeleev Commun., 25:1 (2015),  17–18
  22. 2-(2-Ethynyl-1-aziranyl)-3,4-dihydro-2H-pyrrole: a one-pot assembly from isopropyl phenyl ketoxime and acetylene during the synthesis of 3H-pyrrole

    Mendeleev Commun., 24:6 (2014),  368–369
  23. Synthesis of 3,3-dimethyl-2-phenyl-3H-pyrrole from Isopropyl Phenyl Ketoxime and Acetylene: A Side Formation of 4,4-dimethyl-5-phenyl-1-vinyl-2-pyrrolidinone as Clue to the Reaction Mechanism

    Mendeleev Commun., 24:2 (2014),  100–101
  24. Reactions of acetylenes in superbasic media. Recent advances

    Usp. Khim., 83:7 (2014),  600–619
  25. One-pot synthesis of 3-(E)-styrylpyrroles from (E)-styrylmethyl ketoximes and acetylene

    Mendeleev Commun., 23:6 (2013),  340–341
  26. Superbase-catalyzed addition of ketones to propargyl and allenyl ethers in the KOH (KOBut)/DMSO system

    Mendeleev Commun., 23:4 (2013),  204–205
  27. Modification of g-Aminobutyric Acid with Acylacetylenes: Stereoselective C-Vinylation of the Primary Adducts and Transformation to Acylpyridines

    Mendeleev Commun., 22:6 (2012),  314–316
  28. Consecutive Reactions of Dialkyl Ethynyl Carbinols with Acetylene in Superbase KOH/DMSO Suspension

    Mendeleev Commun., 22:3 (2012),  132–133
  29. Base-catalyzed O-vinylation of tertiary propargylic alcohols with acetylene: First examples

    Mendeleev Commun., 22:2 (2012),  62–63
  30. Stereospecific protonation of pyrrole-2-carboxaldehyde Z-oximes as a result of through-space cation stabilization with oxime hydroxyl

    Mendeleev Commun., 21:2 (2011),  103–105
  31. The reaction of 2-arylazo-1-vinylpyrroles with trifluoroacetic anhydride: unexpected formation of N-aryl-2,2,2-trifluoroacetamides and conjugated polymers

    Mendeleev Commun., 21:1 (2011),  36–37
  32. A peculiar selective rearrangement during the NiS-catalysed dehydrogenation of 4,5-dihydro-1H-benz[g]indole

    Mendeleev Commun., 17:5 (2007),  296–298
  33. Unexpected formation of 4-methyl-1-vinyl-δ-carboline in the reaction of 3-acetylindole oxime with acetylene

    Mendeleev Commun., 17:1 (2007),  40–42
  34. Unexpected formation of 1-vinyl-2-[2′-(6′-methylpyridyl)]pyrrole from dimethylglyoxime and acetylene in the Trofimov reaction

    Mendeleev Commun., 11:2 (2001),  74–75
  35. An unusually fast nucleophilic addition of amidoximes to acetylene

    Mendeleev Commun., 10:1 (2000),  29–30
  36. Trifluoroacetylation of O-vinyl acetoxime

    Mendeleev Commun., 9:6 (1999),  238–239
  37. Synthesis of 1H- and 1-vinyl-2-pyridylpyrroles by the Trofimov reaction

    Mendeleev Commun., 7:4 (1997),  162–163


© Steklov Math. Inst. of RAS, 2026