The Synthesis of Trisubstituted Pyridines via Kröhnke Reaction
A. Basnet, P. Thapa, R. Karki, Y. Na, Y. Jahng, B.-S. Jeong, T. C. Jeong, C.-S. Lee, E.-S. Lee*
Yeungnam University and Catholic Universtiy of Daegu, Kyongsan, Korea
23. August 2007 (online)
Various 2,4,6-trisubstituted pyridine derivatives have been synthesized using modified Kröhnke reaction conditions. These compounds were evaluated for their Topo I and II inhibitory activity and antitumor cytotoxicity against several human cancer cell lines and found that heterocyclic moieties are important at 2- and 4-positions on the central pyridine ring system to display these activities. There was no direct correlation between antitumor cytotoxicity and topoisomerase inhibitory activity.