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Chemistry of Heterocyclic Compounds

, Volume 54, Issue 9, pp 875–886 | Cite as

SNH Arylamination of Nitroquinolines: Access to Nitro and Nitroso Derivatives of Arylaminoquinolines

  • Oleg P. Demidov
  • Diana Yu. Pobedinskaya
  • Elena K. Avakyan
  • Gulminat A. Amangasieva
  • Ivan V. Borovlev
Article
  • 18 Downloads

SNH Arylamination of 5-, 6-, 7-, and 8-nitroquinolines in anhydrous DMSO gave not only the arylamino derivatives of the respective nitroquinolines, but also the arylamino derivatives of nitrosoquinolines. In the case of 6-nitroquinoline, the first representatives of polycyclic structures on the basis of pyrido[3,2-a]phenazine 7-oxide were isolated.

Keywords

nitroquinolines phenazines SNH arylamination disproportionation SNH methodology 

Notes

This work was performed with financial support from the Ministry of Education and Science of the Russian Federation within the framework of State Assignment (project No. 4.6306.2017/8.9).

Supplementary material

10593_2018_2368_MOESM1_ESM.pdf (9.3 mb)
ESM 1 (PDF 9547 kb)

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  • Oleg P. Demidov
    • 1
  • Diana Yu. Pobedinskaya
    • 1
  • Elena K. Avakyan
    • 1
  • Gulminat A. Amangasieva
    • 1
  • Ivan V. Borovlev
    • 1
  1. 1.North-Caucasus Federal UniversityStavropolRussia

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