articleOrganic LettersJan 20, 2026Closed access

Catalytic Atroposelective Synthesis of C–N Axially Chiral Pyrazolyl Pyrroles via De Novo Construction of a Pyrrole Ring

Jiangsu Normal University · Changzhou University

PubMed
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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.

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Authors

5

Topics & keywords

Keywords
  • Axial symmetry
  • Pyrrole
  • Catalysis
  • Ring (chemistry)
  • Pyrazole
  • Axial chirality
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