Abstract
A straightforward assembly of polysubstituted 1,2-dihydro-3H-pyrrolo[1,2-a]indol-3-ones through a domino palladium-catalyzed reaction of indol-2-ylmethyl acetates with 1,3-dicarbonyl derivatives is described. The key role of the features of the 1,3-dicarbonyls on the reaction outcome has been explored. The employment of 2-methylcyclohexan-1,3-dione as the dicarbonyl source could allow further challenging indole nucleus functionalizations.
| Lingua originale | Inglese |
|---|---|
| pagine (da-a) | 1516-1533 |
| Numero di pagine | 18 |
| Rivista | Catalysts |
| Volume | 12 |
| Numero di pubblicazione | 12 |
| DOI | |
| Stato di pubblicazione | Pubblicato - 2022 |
All Science Journal Classification (ASJC) codes
- Catalisi
- Scienze Ambientali Generali
- Chimica Fisica e Teorica
Keywords
- 1
- 2-a]indol-3-ones
- 2-dihydro-3H-pyrrolo[1
- domino reactions
- indolyl methides
- palladium catalysis