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Palladium‐Catalyzed Inert C−H Bond Activation and Cyclocarbonylation of Isoquinolones with Carbon Dioxide Leading to Isoindolo[2,1‐b]isoquinoline‐5,7‐Diones.
- Source :
-
Advanced Synthesis & Catalysis . Jul2019, Vol. 361 Issue 13, p3080-3085. 6p. - Publication Year :
- 2019
-
Abstract
- A palladium‐catalyzed inert C−H bond activation and cyclocarbonylation of isoquinolones leading to isoindolo[2,1‐b]isoquinoline‐5,7‐diones under 1 atm of carbon dioxide has been developed. This transformation features high regio‐ and chemo‐selectivity, step‐economy, and good functional group tolerance. Most of the corresponding products were obtained in moderate to good yields. It offers an alternative approach for the synthesis of useful diverse isoindolo[2,1‐b]isoquinoline‐5,7‐dione derivatives. [ABSTRACT FROM AUTHOR]
- Subjects :
- *CARBON dioxide
*LEAD dioxide
*PALLADIUM
*FUNCTIONAL groups
Subjects
Details
- Language :
- English
- ISSN :
- 16154150
- Volume :
- 361
- Issue :
- 13
- Database :
- Academic Search Index
- Journal :
- Advanced Synthesis & Catalysis
- Publication Type :
- Academic Journal
- Accession number :
- 137773930
- Full Text :
- https://doi.org/10.1002/adsc.201900305