59046-00-3Relevant academic research and scientific papers
REACTION OF DIHALOCARBENES WITH 2-(BENZYLIDENEAMINO)PYRIDINES. CYCLIZATION OF 2-(BENZYLIDENEAMINO)PYRIDINIUM DIHALOMETHYLIDS TO GIVE 2-ARYL-3-HALOIMIDAZOPYRIDINES
Khlebnikov, A. F.,Kostik, E. I.,Kostikov, R. R.
, p. 636 - 642 (2007/10/02)
Pyridinium dichloromethylids, formed in the reaction of dichlorocarbene with 2-(benzylideneamino)pyridines, undergo intramolecular 1,5-cyclization to give 2-aryl-8-chloroimidazopyridines, which undergo partial conversion to 2-aryl-3-chloro-4H-pyrid
Studies on Ketene and Its Derivatives. Part 119. . Reactions of Haloketenes with 2-Arylideneaminopyridines
Katagiri, Nobuya,Kato, Tetsuzo,Niwa, Ryuji
, p. 407 - 412 (2007/10/02)
Reactions of haloketenes with 2-arylideneaminopyridines were examined.Reaction of dichloroketene with 2-benzylideneaminopyridines gave 2,2-dichloro-3-phenyl-3-(2-pyridylamino)propanoic acids and 3-chloro-2-phenylpyridopyrimidin-4(4H)-ones.Similar r
