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Regioselective Construction of Indolylated Cyclic Tetrasubstituted Carbon Centers through Brønsted Acid‐Catalyzed Dearomative Skeletal Rearrangement of Azofurans.
- Source :
-
Advanced Synthesis & Catalysis . 11/7/2023, Vol. 365 Issue 21, p3718-3723. 6p. - Publication Year :
- 2023
-
Abstract
- A Brønsted acid‐catalyzed dearomative skeletal rearrangement of azofurans with indoles is reported, enabling a regioselective 1,6‐addition, ring‐opening and 1,4‐addition cascade to produce 26 examples of indolylated pyrrol‐2‐ones with a cyclic tetrasubstituted stereocenter in 58–94% yields. This protocol demonstrates remarkable compatibility regarding azofurans and indoles with different substitution patterns, featuring complete regioselectivity. [ABSTRACT FROM AUTHOR]
- Subjects :
- *CARBON
*INDOLE compounds
*INDOLE
Subjects
Details
- Language :
- English
- ISSN :
- 16154150
- Volume :
- 365
- Issue :
- 21
- Database :
- Academic Search Index
- Journal :
- Advanced Synthesis & Catalysis
- Publication Type :
- Academic Journal
- Accession number :
- 173486283
- Full Text :
- https://doi.org/10.1002/adsc.202300948