Enantioselective Synthesis of C–N Atropisomeric Pyrazole–Pyrroles via Asymmetric Paal–Knorr Reaction

The catalytic asymmetric construction of bis‐five‐membered C–N axially chiral scaffolds remains challenging, owing to their low rotational energy barriers. Herein, we describe a chiral phosphoric acid‐catalyzed asymmetric Paal–Knorr reaction between N ‐alkyl 5‐aminopyrazoles and 1,4‐diketones, affording ortho ‐trisubstituted C–N axially chiral pyrazole–pyrroles in high yield and excellent enantioselectivity. Moreover, the successful construction of ortho ‐trisubstituted pyrazole–pyrrole atropisomers is attributed to the strategic use of sterically bulky N ‐alkyl pyrazoles for effective stereocontrol. This protocol not only expands the repertoire of bis‐five‐membered C–N axially chiral scaffolds but also exhibits facile scale‐up and diverse late‐stage functionalizations, underscoring its synthetic utility.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2026-04-24
DOI
https://doi.org/10.1002/adsc.70431
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
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article

Enantioselective Synthesis of C–N Atropisomeric Pyrazole–Pyrroles via Asymmetric Paal–Knorr Reaction

Wenxuan Zhang, Yuhuan Yang, Chen Dong, Wenjing Qiu et al.
Advanced Synthesis & Catalysis
Axial and Atropisomeric Chirality Synthesis
article

Enantioselective Synthesis of C–N Atropisomeric Pyrazole–Pyrroles via Asymmetric Paal–Knorr Reaction

Wenxuan Zhang, Yuhuan Yang, Chen Dong, Wenjing Qiu, Tao Liu
article en

Abstract

The catalytic asymmetric construction of bis‐five‐membered C–N axially chiral scaffolds remains challenging, owing to their low rotational energy barriers. Herein, we describe a chiral phosphoric acid‐catalyzed asymmetric Paal–Knorr reaction between N ‐alkyl 5‐aminopyrazoles and 1,4‐diketones, affording ortho ‐trisubstituted C–N axially chiral pyrazole–pyrroles in high yield and excellent enantioselectivity. Moreover, the successful construction of ortho ‐trisubstituted pyrazole–pyrrole atropisomers is attributed to the strategic use of sterically bulky N ‐alkyl pyrazoles for effective stereocontrol. This protocol not only expands the repertoire of bis‐five‐membered C–N axially chiral scaffolds but also exhibits facile scale‐up and diverse late‐stage functionalizations, underscoring its synthetic utility.

Advanced Synthesis & CatalysisVol. 368(9)
Jining University (CN)
Affordable and clean energy
Openalex Percentile: Top 8%
Axial and Atropisomeric Chirality Synthesis
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