## Abstract The novel method is performed in the presence of either a catalytic or stoichiometric amount of HI.
Synthesis of 9,9-Disubstituted 9H-Pyrrolo[1,2-a]indoles by Hydriodic Acid-Catalyzed Cyclization of 1-[2-(1-Aryl(or methyl)ethenyl)phenyl]-1H-pyrroles
✍ Scribed by Kazuhiro Kobayashi; Kenichi Hashimoto; Hiroo Hashimoto; Hideaki Kondo; Hisatoshi Konishi
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- German
- Weight
- 152 KB
- Volume
- 94
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
A novel method is reported for the synthesis of 9,9‐disubstituted 9__H__‐pyrrolo[1,2‐a]indoles. Cyclization of 1‐[2‐(1‐aryl(or methyl)ethenyl)phenyl]‐1__H__‐pyrroles, which can be easily prepared from 2‐(1‐aryl(or methyl)ethenyl)anilines, proceeds smoothly, in general, at 0° in the presence of a catalytic (or an equimolar) amount of HI in MeCN to provide the desired products.
📜 SIMILAR VOLUMES
## Abstract The N‐substituted 1‐benzimidazolyl‐succinimides **6a**–**v** (Scheme 1, Table 1 and 2) have been prepared by the reaction of benzimidazole and its derivatives with maleimides. Reduction of the N‐cyclohexyl and N‐cyclo‐octyl substituted 1‐benzimidazolyl‐succinimides **6i**–**k** with lit