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Nosova Emiliya Vladimirovna

Publications in Math-Net.Ru

  1. Synthesis of novel 8-nitro-substituted 1,3-benzothiazin-4-ones

    Mendeleev Commun., 30:4 (2020),  427–429
  2. Nucleophilic substitution of hydrogen–the Boger reaction sequence as an approach towards 8-(pyridin-2-yl)coumarins

    Mendeleev Commun., 29:3 (2019),  299–300
  3. Pericyclic reactions in the synthesis of new 5-aryl-5,6-dihydroquinolino[2,1-b]quinazolin-12-ones

    Mendeleev Commun., 29:2 (2019),  135–137
  4. Functionalized benzazines as luminescent materials and components for optoelectronics

    Usp. Khim., 88:11 (2019),  1128–1178
  5. Organofluorine chemistry: promising growth areas and challenges

    Usp. Khim., 88:5 (2019),  425–569
  6. Synthesis and photophysical studies of novel 4-aryl substituted 2-phenyl-, 2-(fluoren-2-yl)- and 2-cymantrenylquinazolines

    Mendeleev Commun., 28:1 (2018),  33–35
  7. Synthesis and photophysical studies of novel 2-[5-(4-diethylaminophenyl)thiophen-2-yl]quinazoline derivatives

    Mendeleev Commun., 28:1 (2018),  14–16
  8. Cyclometallated PTII complexes of 2-(2-thienyl)-4-(cycloalkylimino)-substituted quinazolines

    Mendeleev Commun., 26:2 (2016),  129–130
  9. Synthesis and antitumour activity of 4-aminoquinazoline derivatives

    Usp. Khim., 85:7 (2016),  759–793
  10. Aryne approach towards 2,3-difluoro-10-(1H-1,2,3-triazol-1-yl)pyrido[1,2-a]indoles

    Mendeleev Commun., 25:1 (2015),  13–14
  11. Chemosensors for detection of nitroaromatic compounds (explosives)

    Usp. Khim., 83:9 (2014),  783–819
  12. Azinylarylethenes: synthesis and photophysical and photochemical properties

    Usp. Khim., 80:11 (2011),  1166–1184
  13. Fluorine-containing quinazolines and their oxa and thia analogues: synthesis and biological activities

    Usp. Khim., 78:5 (2009),  421–441
  14. New approach to [a]-fused fluoroquinolones: the synthesis of 5-oxo-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinolines

    Mendeleev Commun., 11:2 (2001),  53–54
  15. 1,3,4-Oxa(thia)diazino [i,j]-annelated quinolines: a new type of key intermediate in the synthesis of tricyclic fluoroquinolones

    Mendeleev Commun., 8:4 (1998),  131–133
  16. Novel pentacyclic fluoroquinolones

    Mendeleev Commun., 7:3 (1997),  109–110


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