Regioselective three-component synthesis of novel indeno[1,2-b]-pyrazolo[4,3-e]pyridines-fused derivatives of 4-azafluorenone alkaloid
✍ Scribed by Jairo Quiroga; Débora Cobo; Braulio Insuasty; Rodrigo Abonía; Silvia Cruz; Manuel Nogueras; Justo Cobo
- Book ID
- 102340266
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2008
- Tongue
- English
- Weight
- 335 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
magnified image
New fused indeno[1,2‐b]pyridine derivatives have been prepared in a multicomponent reaction from benzaldehydes, indanedione and the appropriate aminoheteroaryl compound. The simple methodology permitted the syntheses of a series of indeno[1,2‐b]pyrazolo[4,3‐e]pyridines 4 from 5‐aminopyrazol 1 and modulated by the corresponding benzaldehyde 2.
📜 SIMILAR VOLUMES
## Abstract magnified image A series of new indeno[1,2‐__b__]pyrazolo[4,3‐__e__]pyridin‐5(1__H__)‐one derivatives were synthesized by three‐component reactions of 1,3‐indandione, 3‐methyl‐1__H__‐pyrazol‐5‐amine, and aldehyde in water under microwave irradiation without any catalyst. J. Heterocyclic