ChemInform Abstract: Formal [4 + 2] Intramolecular Ketenimine—Imine Cycloaddition. Synthesis of Benzimidazo[1,2-b]isoquinolines.
✍ Scribed by Mateo Alajarin; Angel Vidal; Fulgencio Tovar; Carlota Conesa
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 30 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
✦ Synopsis
Formal [4 + 2] Intramolecular Ketenimine-Imine Cycloaddition. Synthesis of Benzimidazo[1,2-b]isoquinolines.
-Formal [4+2] cycloaddition of ketenimine intermediates (V) derived from the azides (III) and diphenylketene (IV) by aza-Wittig reaction, provides the partially saturated compounds (VI). They can be easily aromatized to benzimidazo[1,2b]isoquinolinones (VII).
📜 SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract For Abstract see ChemInform Abstract in Full Text.