## Abstract The synthesis of some new pyrazolo[3โฒ,4โฒ:6,7]azepino[5,4,3โ__cd__] indoles **(10aโc)** was achieved __via__ regiosโelective cyclization of the respective 3โ(4โacylaminopyrazolโ5โyl)indoles **(9aโc)** under BischlerโNapieralski reaction conditions. The latter compounds were obtained by a
Acyltryptamines. IV.1Azepino[5,4,3-cd]indoles
โ Scribed by von Strandtmann, Maximilian; Cohen, Marvin P.; Shavel, John
- Book ID
- 111874747
- Publisher
- American Chemical Society
- Year
- 1965
- Tongue
- English
- Weight
- 642 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0022-2623
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## 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 โFull Textโ option. The original article is trackable v
Monoor dibromo derivatives 2 and 3 were prepared by an efficient two-step route from 10-methyl-azepino [3,4-b]indole-1,5dione 1. Elimination reaction on 2 gave access to 4-bromo-10-methyl-2H,10H-azepino[3,4-b]indole-1,5-diones 4. Finally, 4-substituted 10methyl-2H,10H-azepino [3,4-b]indole-1,5-dione