RUS  ENG
Полная версия
ПЕРСОНАЛИИ

Гусарова Нина Кузьминична

Публикации в базе данных Math-Net.Ru

  1. A mechanistic insight into the chemoselectivity of the reaction between 3-phenyl-2-propynenitrile, secondary phosphine oxides and pyridinoids

    Mendeleev Commun., 31:5 (2021),  670–672
  2. Chemoselective vinylation of aminophenols with acetylene catalyzed by sodium aminophenolates in aqueous DMSO

    Mendeleev Commun., 30:6 (2020),  788–790
  3. Химия фосфорорганических соединений на основе элементного фосфора: достижения и горизонты

    Усп. хим., 89:2 (2020),  225–249
  4. Catalyst-free addition of secondary phosphine chalcogenides to pyrazolecarbaldehydes

    Mendeleev Commun., 29:6 (2019),  683–685
  5. Single-stage synthesis of alkyl-H-phosphinic acids from elemental phosphorus and alkyl bromides

    Mendeleev Commun., 29:3 (2019),  328–330
  6. Solvent-free synthesis of 4-chalcogenophosphorylpyridines via $\mathrm{S_N^HAr}$ reaction of pyridines with secondary phosphine chalcogenides

    Mendeleev Commun., 28:6 (2018),  582–583
  7. 2-Halopyridines in the triple reaction in the Pn/KOH/DMSO system to form tri(2-pyridyl)phosphine: Experimental and quantum-chemical dissimilarities

    Mendeleev Commun., 28:5 (2018),  472–474
  8. Phosphorus halide free synthesis of 1,2,3,4-tetrahydroisophosphinoline 2-oxides

    Mendeleev Commun., 28:1 (2018),  29–30
  9. Перспективные точки роста и вызовы элементоорганической химии

    Усп. хим., 87:5 (2018),  393–507
  10. Structural effect in the reductive vinylation/phosphorylation of pyridines with alkyl propiolates and secondary phosphine chalcogenides: protonation vs. zwitterion generation

    Mendeleev Commun., 27:6 (2017),  553–555
  11. Microwave-assisted catalyst-free addition of secondary phosphines to fullerene C60

    Mendeleev Commun., 27:2 (2017),  198–200
  12. Synthesis of tris[2-(2-furyl)ethyl]phosphine its chalcogenides and Pdii complex

    Mendeleev Commun., 26:4 (2016),  314–316
  13. Unexpected N,N’-coordination of tris(2-pyridyl)-phosphine chalcogenides to PdCl2

    Mendeleev Commun., 25:3 (2015),  196–198
  14. A shortcut to tris[2-(4-hydroxyphenyl)ethyl]phosphine oxide and 2-(4-hydroxyphenyl)ethylphosphinic acid via reaction of elemental phosphorus with 4-tert-butoxystyrene

    Mendeleev Commun., 24:1 (2014),  29–31
  15. Cross-coupling between secondary phosphine selenides and primary or secondary amines: halogen-free synthesis of phosphinoselenoic amides

    Mendeleev Commun., 23:5 (2013),  253–254
  16. Synthesis and Structural Characterization of the First Europium(III) Pyridylphosphine Complex, [Eu(N,N’,N”-2-Py3P)(NO3)3]

    Mendeleev Commun., 22:6 (2012),  294–296
  17. Tris(2-pyridyl)phosphine: a straightforward microwave-assisted synthesis from 2-bromopyridine and red phosphorus and coordination with cobalt(ii) dichloride

    Mendeleev Commun., 22:4 (2012),  187–188
  18. Unexpected redox reaction of alkali metal diselenophosphinates with elemental iodine

    Mendeleev Commun., 22:1 (2012),  18–20
  19. Free-radical addition of phosphine to vinyl ethers: atom-economic synthesis of tris(2-organyloxyethyl)phosphines and their derivatives

    Mendeleev Commun., 21:1 (2011),  17–18
  20. Radical addition of secondary phosphine sulfides and selenides to vinyl tellurides

    Mendeleev Commun., 20:6 (2010),  346–347
  21. Reaction of phosphine with allylbenzene in the KOH–DMSO system: regioselective synthesis of (1-phenylprop-2-yl)phosphine and bis(1-phenylprop-2-yl)phosphine

    Mendeleev Commun., 20:5 (2010),  275–276
  22. Synthesis of vinylphosphine oxides: vinyl selenides as vinylating agents

    Mendeleev Commun., 20:1 (2010),  20–21
  23. Elemental phosphorus in strongly basic media as phosphorylating reagent: a dawn of halogen-free ‘green’ organophosphorus chemistry

    Mendeleev Commun., 19:6 (2009),  295–302
  24. Complex of tris(Z-styryl)phosphine with PdCl2 as a new catalyst for the Sonogashira reaction

    Mendeleev Commun., 18:6 (2008),  318–319
  25. Nucleophilic additon of phosphine to 1-(tert-butyl)-4-vinylbenzene: a short-cut to bulky secondary and tertiary phosphines and their chalcogenides

    Mendeleev Commun., 18:5 (2008),  260–261
  26. Nucleophilic addition of secondary phosphine chalcogenides to, α,β-acetylenic γ-hydroxy acid nitriles and a rearrangement of the adducts

    Mendeleev Commun., 17:6 (2007),  325–326
  27. Free-radical addition of phosphine sulfides to aryl and hetaryl acetylenes: unprecedented stereoselectivity

    Mendeleev Commun., 17:3 (2007),  181–182
  28. Ацетилен: новые возможности классических реакций

    Усп. хим., 76:6 (2007),  550–570
  29. Thiol elimination from tris[2-(phenylthio)ethyl]phosphine oxide: a convenient route to trivinylphosphine oxide

    Mendeleev Commun., 16:1 (2006),  31
  30. Superbase-catalysed addition of methanol to propyne and allene: an expedient synthesis of 2-methoxypropene

    Mendeleev Commun., 16:1 (2006),  13–14
  31. Unexpected double α,β-addition of secondary phosphine chalcogenides to 3-phenyl-2-propynenitrile

    Mendeleev Commun., 15:5 (2005),  183–184
  32. Atom-economic synthesis of tertiary 2-alkoxyethylphosphine sulfides

    Mendeleev Commun., 14:5 (2004),  216–217
  33. Reactions of alkali metal acetylides with red phosphorus

    Mendeleev Commun., 10:2 (2000),  66–67
  34. Addition of secondary phosphines to phenylcyanoacetylene as a route to functional phosphines

    Mendeleev Commun., 9:4 (1999),  163–164
  35. Фосфин в синтезе фосфорорганических соединений

    Усп. хим., 68:3 (1999),  240–253
  36. Cleavage of P–P Bonds in Phosphorus. An Efficient Method for the Preparation of Primary Alkylphosphines

    Mendeleev Commun., 5:1 (1995),  14–15
  37. Системы элементный фосфор–сильные основания в синтезе фосфорорганических соединений

    Усп. хим., 60:12 (1991),  2619–2632


© МИАН, 2026