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Статьи (40)

# Публикация
21 Politanskaya L. , Bagryanskaya I. , Tretyakov E.
Synthesis of polyfluorinated arylhydrazines, arylhydrazones and 3-methyl-1-aryl-1H-indazoles
Journal of Fluorine Chemistry. 2018. V.214. P.48-57. DOI: 10.1016/j.jfluchem.2018.06.011 WOS Scopus РИНЦ OpenAlex
22 Politanskaya L. , Duan Z. , Bagryanskaya I. , Eltsov I. , Tretyakov E. , Xi C.
Highly efficient synthesis of polyfluorinated 2-mercaptobenzothiazole derivatives
Journal of Fluorine Chemistry. 2018. V.212. P.130-136. DOI: 10.1016/j.jfluchem.2018.06.001 WOS Scopus РИНЦ OpenAlex
23 Politanskaya L. , Rybalova T. , Zakharova O. , Nevinsky G. , Tretyakov E.
p-Toluenesulfonic acid mediated one-pot cascade synthesis and cytotoxicity evaluation of polyfluorinated 2-aryl-2,3-dihydroquinolin-4-ones and their Check for updates derivatives
Journal of Fluorine Chemistry. 2018. V.211. P.129-140. DOI: 10.1016/j.jfluchem.2018.04.005 WOS Scopus РИНЦ OpenAlex
24 Tretyakov E.V. , Makhneva T.V. , Politanskaya L.V. , Bagryanskaya I.Y. , Stass D.V.
Molecular and Crystal Structure of 2-Amino-Polyfluorophenyl-4,4,5,5-Tetramethyl-4,5-Dihydro-1H-Imidazol-3-Oxide-1-Oxyls
Journal of Structural Chemistry. 2018. V.59. N3. P.689-696. DOI: 10.1134/S0022476618030289 WOS Scopus РИНЦ OpenAlex
25 Politanskaya L.V. , Shteingarts V.D. , Tretyakov E.V.
General and efficient synthesis of polyfluorinated 2-aminotolans and 2-arylindoles
Journal of Fluorine Chemistry. 2016. V.188. P.85-98. DOI: 10.1016/j.jfluchem.2016.06.010 WOS Scopus РИНЦ OpenAlex
26 Bagryanskaya I.Y. , Politanskaya L.V. , Tretyakov E.V.
Frequently used, but still unknown: Terbium(III) tris-hexafluoroacetylacetonate dihydrate
Inorganic Chemistry Communications. 2016. V.66. P.47-50. DOI: 10.1016/j.inoche.2016.02.009 WOS Scopus РИНЦ OpenAlex
27 Politanskaya L.V. , Chuikov I.P. , Tretyakov E.V. , Shteingarts V.D. , Ovchinnikova L.P. , Zakharova O.D. , Nevinsky G.A.
An effective two-step synthesis, fluorescent properties, antioxidant activity and cytotoxicity evaluation of benzene-fluorinated 2,2-dimethyl-2,3-dihydro-1H-quinolin-4-ones
Journal of Fluorine Chemistry. 2015. V.178. P.142-153. DOI: 10.1016/j.jfluchem.2015.07.006 WOS Scopus РИНЦ OpenAlex
28 Zakharova O. , Troshkova N. , Politanskaya L. , Ovchinnikova L. , Tretyakov E. , Shteingarts V. , Nevinsky G.
Cytotoxicity of new polyfluorinated 1,4-naphtoquinones containing aminoacid substituents and benzene fluorinated 2,2-Dimethyl-2,3-dihydro-1H-quinoline-4-ones
FEBS JOURNAL. 2015. V.282. NSI. LB-171 . WOS
29 Politanskaya L. , Shteingarts V. , Tretyakov E. , Potapov A.
The p-toluenesulfonic acid-catalyzed transformation of polyfluorinated 2-alkynylanilines to 2-aminoaryiketones and indoles
Tetrahedron Letters. 2015. V.56. N39. P.5328-5332. DOI: 10.1016/j.tetlet.2015.07.078 WOS Scopus РИНЦ OpenAlex
30 Politanskaya L.V. , Chuikov I.P. , Shteingarts V.D.
Synthesis of indoles with a polyfluorinated benzene ring
Tetrahedron. 2013. V.69. N39. P.8477-8486. DOI: 10.1016/j.tet.2013.07.037 WOS Scopus РИНЦ OpenAlex
31 Potapov A.G. , Politanskaya L.V.
The study of the adsorption of 1,3-diethers on the MgCl2 surface
Journal of Molecular Catalysis A: Chemical. 2013. V.368. P.159-162. DOI: 10.1016/j.molcata.2012.12.004 WOS Scopus РИНЦ OpenAlex
32 Politanskaya L.V. , Chuikov I.P. , Kolodina E.A. , Shvartsberg M.S. , Shteingarts V.D.
Synthesis of polyfluorinated ortho-alkynylanilines
Journal of Fluorine Chemistry. 2012. V.135. P.97-107. DOI: 10.1016/j.jfluchem.2011.09.008 WOS Scopus РИНЦ OpenAlex
33 Reshetov A.V. , Selivanova G.A. , Politanskaya L.V. , Beregovaya I.V. , Shchegoleva L.N. , Vasil'eva N.V. , Bagryanskaya I.Y. , Shteingarts V.D.
Hydrodefluorination of N-acetylheptafluoro-2-naphthylamine by zinc in aqueous ammonia: synthetic outcomes and mechanistic considerations
ARKIVOC. 2011. P.242-262. DOI: 10.3998/ark.5550190.0012.818 WOS Scopus РИНЦ OpenAlex
34 Politanskaya L. , Malysheva L. , Beregovaya I. , Bagryanskaya I. , Gatilov Y. , Malykhin E. , Shteingarts V.
Regioselectivity and relative substrate activity of difluoroquinolines containing fluorine atoms in benzene ring in reaction with sodium methoxide
Journal of Fluorine Chemistry. 2005. V.126. N11-12. P.1502-1509. DOI: 10.1016/j.jfluchem.2005.08.010 WOS Scopus РИНЦ OpenAlex
35 Politanskaya L. , Malykhin E. , Shteingarts V.
The influence of nucleophile substituents on the orientation in the reaction between 2,3-difluoronitrobenzene and lithium phenoxides in liquid ammonia
European Journal of Organic Chemistry. 2001. V.2001. N2. P.405-411. DOI: 10.1002/1099-0690(200101)2001:2<405::AID-EJOC405>3.0.CO;2-6 WOS Scopus РИНЦ OpenAlex
36 Politanskaya L.V. , Ryabitskaya E.V. , Malykhin E.V. , Steingartz V.D.
Reactions of aromatic compounds with nucleophilic reagents in liquid ammonia: XVII. Effect of ionic association on the orientation in aryloxydefluorination of 2,4-difluoronitrobenzene
Russian Journal of Organic Chemistry. 2000. V.36. N6. P.801-807. DOI: 10.1007/BF02757434 WOS Scopus РИНЦ OpenAlex
37 Politanskaya L.V. , Malykhin E.V. , Shteingarts V.D.
Reactions of Aromatic Compounds with Nucleophilic Reagents in Liquid Ammonia. XVI. Thermodynamic Aspects of Orientation in Reactions of 2,4-Difluoronitrobenzene with Substituted Lithium Phenoxides
Russian Journal of Organic Chemistry. 1997. V.33. N5. P.644-651. Scopus РИНЦ
38 Politanskaya L.V. , Malykhin E.V. , Shteingarts V.D.
Interaction of aromatic compounds with nucleophilic reagents in liquid ammonia .16. Thermodynamic aspects of orientation in 2,4-difluoronitrobenzene reactions with lithium substituted phenolates
Журнал органической химии (RUSS J ORG CHEM+). 1997. V.33. N5. P.703-710. WOS
39 Politanskaya L.V. , Malykhin E.V.
Analysis of medium influence on substituent effects in equilibrium phenol dissociation
Журнал органической химии (RUSS J ORG CHEM+). 1996. V.32. N8. P.1165-1173. WOS
40 Politanskaya L.V. , Malykhin E.V. , Shteingarts V.D.
Interaction of aromatic compounds with nucleophilic reagents in liquid ammonium .14. Effect of liquid ammonium as a solvent on the dependence of 2,4-difluoronitrobenzene phenoxydefluorination orientation on the substituent nature in nucleophile
Журнал органической химии (RUSS J ORG CHEM+). 1996. V.32. N8. P.1174-1185. WOS

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