Efficient Synthesis of 2-Unsubstituted 1,3-Selenazoles.
β Scribed by Karlheinz Geisler; Andreas Kuenzler; Harald Below; Ehrenfried Bulka; Wolf-Diethard Pfeiffer; Peter Langer
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 140 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract The reaction of __N__,__Nβ²__βdiarylselenoureas **16** with phenacyl bromide in EtOH under reflux, followed by treatment with NH~3~, gave __N__,3βdiarylβ4βphenylβ1,3βselenazolβ2(3__H__)βimines **13** in high yields (__Schemeβ 2__). A reaction mechanism __via__ formation of the correspondi
2-Dialkylamino-1,3-selenazoles were yielded by the reaction of N,N-unsubstituted selenoureas with ketones in the presence of ferric chloride.
## Abstract For Abstract see ChemInform Abstract in Full Text.