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Photoinduced Dehalocyclization to Access Oxindoles Using Formate as a Reductant.
- Source :
-
Chinese Journal of Chemistry . Jun2024, Vol. 42 Issue 11, p1203-1208. 6p. - Publication Year :
- 2024
-
Abstract
- Comprehensive Summary: Herein, we report an efficient and practical protocol for the photoinduced dehalocyclization of ortho‐halophenylacrylamides with formate by the engagement of a CO2 radical anion to access substituted oxindoles. This method proceeds smoothly under mild conditions and exhibits a wide range of substrate as well as remarkable functional group compatibility. [ABSTRACT FROM AUTHOR]
- Subjects :
- *OXINDOLES
*RADICAL anions
*RADICAL ions
*FUNCTIONAL groups
*CARBON dioxide
Subjects
Details
- Language :
- English
- ISSN :
- 1001604X
- Volume :
- 42
- Issue :
- 11
- Database :
- Academic Search Index
- Journal :
- Chinese Journal of Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 176927000
- Full Text :
- https://doi.org/10.1002/cjoc.202300740