Isocyanate acting as a carbonyl precursor: pyridyl group-assisted formation of 4 H-pyrido [1, 2-a] pyrimidin-4-ones from ketimines and isocyanates
Y Kuninobu, S Nishimura, K Takai
Index: Kuninobu, Yoichiro; Nishimura, Shuhei; Takai, Kazuhiko Organic and Biomolecular Chemistry, 2006 , vol. 4, # 2 p. 203 - 205
Full Text: HTML
Citation Number: 4
Abstract
By the reactions of ketimines bearing a pyridyl or a picolyl group on a nitrogen atom of the imine moiety with tosylisocyanate, 4H-pyrido [1, 2-a] pyrimidin-4-one derivatives could be obtained in quantitative yields. In these reactions, tosylisocyanate acts as a carbonyl precursor. The pyridyl or picolyl group is a key functional group because it is not only the constituent structure of the 4H-pyrido [1, 2-a] pyrimidin-4-one framework but also the ...
Related Articles:
[Hermecz; Podanyi; Meszaros; et al. Journal of Heterocyclic Chemistry, 1983 , vol. 20, # 1 p. 93 - 96]