Efficient [5 + 1]-strategy for the assembly of 1,8-naphthyridin-4(1H)-ones by domino amination/conjugate addition reactions of 1-(2-chloropyridin-3-yl)prop-2-yn-1-ones with amines.
Viktor O Iaroshenko, Ingo Knepper, Muhammad Zahid, Rene Kuzora, Sergii Dudkin, Alexander Villinger, Peter Langer
Index: Org. Biomol. Chem. 15th ed., 10 , 2955-2959, (2012)
Full Text: HTML
Abstract
A facile synthetic approach for the synthesis of 1,8-naphthyridine-4(1H)-one derivatives via a catalyst free and Pd-supported tandem amination sequence is developed and described. In a case of aliphatic amines reaction proceeds in a catalyst free mode, however anilines demand Pd-supported reaction conditions.This journal is © The Royal Society of Chemistry 2012
Related Compounds
Related Articles:
Ruthenium(0)-catalyzed sp3 C-H bond arylation of benzylic amines using arylboronates.
2012-04-06
[Org. Lett. 7th ed., 14 , 1930-1933, (2012)]
2012-05-07
[Chem. Commun. (Camb.) 36th ed., 48 , 4332-4334, (2012)]
2012-05-01
[Magn. Reson. Chem. 5th ed., 50 , 379-387, (2012)]
2006-12-08
[J. Org. Chem. 71 , 9522, (2006)]
Synthesis of terphenyl benzimidazoles as tubulin polymerization inhibitors.
2012-04-01
[Eur. J. Med. Chem. 50 , 9-17, (2012)]