SYNTHESIS OF 2,2'-QUINOCYANINES WITH LONG N-ALKYL SUBSTITUENTS

Authors

  • Н. А. Орлова N. N. Vorozhtsov Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090
  • E. Ф. Колчина N. N. Vorozhtsov Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090
  • Ф. А. Журавлев N. N. Vorozhtsov Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090
  • М. М. Шакиров N. N. Vorozhtsov Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090
  • Т. Н. Герасимова N. N. Vorozhtsov Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090
  • В. B. Шелковников N. N. Vorozhtsov Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090

Keywords:

N-alkyl groups, 2,2'-quinocyanines, 1H NMR spectroscopy

Abstract

2,2'-Quinocyanines with long alkyl substituents on one or both nitrogen atoms have been synthesized. 1H NMR spectroscopy has been used to study the processes occurring during the alkylation of the starting quinoline bases.

How to Cite
Orlova, N. A.; Kolchina, E. F.; Zhuravlev, F. A.; Shakirov, M. M.; Gerasimova, T. N.; Shelkovnikov, V. V. Chem. Heterocycl. Compd. 2002, 38, 1233. [Khim. Geterotsikl. Soedin. 2002, 1399.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1021785630927

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Published

2002-10-25

Issue

No. 10 (2002)

Section

Original Papers