ARYLAMINATION OF 1,3,7-TRIAZAPYRENE

Authors

  • И. В. Боровлев North Caucasus Federal University
  • О. П. Демидов North Caucasus Federal University
  • Н. А. Сайгакова North Caucasus Federal University

DOI:

https://doi.org/10.1007/1249

Keywords:

1, 3, 7-triazapyrenes, ipso substitution of methoxy groups, nucleophilic substitution of hydrogen, oxidative arylamination

Abstract

6‑Aryl(hetaryl)amino-1,3,7-triazapyrenes were prepared by direct oxidative nucleophilic substitution of hydrogen. Nucleophilic ipso substitution of methoxy groups gave 6,8-bis(aryl(hetaryl)amino)-1,3,7-triazapyrenes.

How to Cite
Borovlev, I. V.; Demidov, O. P.; Saigakova, N. A. Chem. Heterocycl. Compd. 2014, 50, 685. [Khim. Geterotsikl. Soedin. 2014, 746.]

For this article in the English edition see DOI 10.1007/s10593-014-1521-4

Author Biographies

И. В. Боровлев, North Caucasus Federal University

Иван Васильевич Боровлев

профессор кафедры химии

О. П. Демидов, North Caucasus Federal University

Олег Петрович Демидов

доцент кафедры химии

Н. А. Сайгакова, North Caucasus Federal University

Надежда Анатольевна Сайгакова

Доцент кафедры химии

Published

2013-12-17

Issue

Section

Original Papers