Studies with enaminones: Reactivity of 1,5-disubstituted-1,4-pentadien-3-ones toward electrophilic reagents. A novel route to azolylazines, benzofuranals, pyranones

Citation
S. Al-mousawi et al., Studies with enaminones: Reactivity of 1,5-disubstituted-1,4-pentadien-3-ones toward electrophilic reagents. A novel route to azolylazines, benzofuranals, pyranones, J HETERO CH, 38(4), 2001, pp. 949-953
Citations number
13
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF HETEROCYCLIC CHEMISTRY
ISSN journal
0022152X → ACNP
Volume
38
Issue
4
Year of publication
2001
Pages
949 - 953
Database
ISI
SICI code
0022-152X(200107/08)38:4<949:SWERO1>2.0.ZU;2-F
Abstract
Several new enaminodienones prepared from substituted acetone and dimethylf ormamide dimethylacetal were used as precursors for synthesis of pyridines, pyranones and benzofurans.