DEVELOPMENT OF THE CATALYTIC SYNTHESIS OF COMPOUNDS OF THE QUINOLINE SERIES (THE N. S. KOZLOV REACTION)

Authors

  • Н. Г. Козлов Institute of Physical Organic Chemistry, Academy of Sciences of Belarus
  • К. Н. Гусак Institute of Physical Organic Chemistry, Academy of Sciences of Belarus
  • А. П. Кадуцкий Institute of Physical Organic Chemistry, Academy of Sciences of Belarus

DOI:

https://doi.org/10.1007/2960

Keywords:

azaphenanthrenes, azomethines, benzoacridones, benzoquinolines, quinaldine, quinolines, phenanthrolines, CH acids, bactericides, luminophores

Abstract

This article is dedicated to the 80th anniversary of the Institute of Physical Organic Chemistry, National Academy of Sciences of Belarus (in 1929-1959 the Institute of Chemistry, Academy of Sciences of the BSSR). It contains a review of the advances in the synthesis and properties of condensed heterocyclic systems containing a quinoline fragment – derivatives of quinaldine, benzo[f]quinoline, indeno- and indoloquinoline, benzo[a]phenanthridine, benzoacridine, tetrahydroquinoline, 1,7- and 4,7-phenanthroline. The reactions forming the basis of the synthesis of the heterocycles are described – catalytic reaction of amines with acetylene, catalytic condensation of azomethines with methyl and α-methylene ketones, triple-component condensation of arylamines, carbonyl compounds, and CH acids.

How to Cite
Kozlov, N. G.; Gusak, K. N.; Kadutskii, A. P. Chem. Heterocycl. Compd. 2010, 46, 505. [Khim. Geterotsikl. Soedin. 2010, 643.]

For this article in the English edition see DOI 10.1007/s10593-010-0540-z

Published

2016-01-14

Issue

Section

Review Articles