Catalytic Atroposelective Synthesis of C–N Axially Chiral Pyrazolyl Pyrroles via De Novo Construction of a Pyrrole Ring
Jiangsu Normal University · Changzhou University
Abstract
The catalytic atroposelective synthesis of five–five-membered C–N axially chiral heterobiaryls featuring the de novo construction of a pyrrole ring was reported. This chiral phosphoric-acid-catalyzed asymmetric Paal–Knorr reaction of 5-aminopyrazoles with 1,4-diketones delivered C–N axially chiral pyrazolyl pyrroles in good yields (up to 96%) with excellent enantioselectivities (up to 97% ee). This work establishes an efficient strategy for constructing five–five-membered C–N axially chiral pyrazole scaffolds and enriches the family of C–N axially chiral molecules.
Citation impact
- FWCI
- 36.08
- Percentile
- 100%
- References
- 61
Authors
5- YCYuyu Chen
Jiangsu Normal University
- JXJia Xue
Jiangsu Normal University
- QSQi Shi
Jiangsu Normal University
- YZYu-Chen ZhangCorresponding
Jiangsu Normal University
- FSFeng ShiCorresponding
Jiangsu Normal University, Changzhou University
Topics & keywords
- Axial symmetry
- Pyrrole
- Catalysis
- Ring (chemistry)
- Pyrazole
- Axial chirality