Copper‐Catalyzed Domino Synthesis of Spiropyrazoline Oxindoles via Condensation of Indolin‐2‐One and Phenylhydrazine Derivatives

Abstract We report a straightforward and efficient method for the synthesis of spiropyrazoline oxindoles using CuCl 2 as the Lewis acid catalyst. This approach involves a one‐pot domino process, consisting of a condensation step between indolin‐2‐one and phenylhydrazine derivatives, followed by a copper‐catalyzed cyclization reaction. The methodology enabled the synthesis of 34 diversely functionalized spiro compounds with yields ranging from moderate to excellent, achieving up to 98%.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-03-11
DOI
https://doi.org/10.1002/adsc.202500223
Citations
1
Primary Topic
Synthesis and Biological Evaluation
Type
article
Field-Weighted Citation Impact
0.94
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article

Copper‐Catalyzed Domino Synthesis of Spiropyrazoline Oxindoles via Condensation of Indolin‐2‐One and Phenylhydrazine Derivatives

Jun Yan, Pascal Retailleau, Abdallah Hamzé, Christine Tran
1 citations
Advanced Synthesis & Catalysis
Synthesis and Biological Evaluation
0.94
article

Copper‐Catalyzed Domino Synthesis of Spiropyrazoline Oxindoles via Condensation of Indolin‐2‐One and Phenylhydrazine Derivatives

Jun Yan, Pascal Retailleau, Abdallah Hamzé, Christine Tran
article en
1 citations

Abstract

Abstract We report a straightforward and efficient method for the synthesis of spiropyrazoline oxindoles using CuCl 2 as the Lewis acid catalyst. This approach involves a one‐pot domino process, consisting of a condensation step between indolin‐2‐one and phenylhydrazine derivatives, followed by a copper‐catalyzed cyclization reaction. The methodology enabled the synthesis of 34 diversely functionalized spiro compounds with yields ranging from moderate to excellent, achieving up to 98%.

Advanced Synthesis & CatalysisVol. 367(10)
Centre National de la Recherche Scientifique (FR), Institut de Chimie des Substances Naturelles (FR), Université Paris-Saclay (FR)
Openalex Percentile: Top 28%
Synthesis and Biological Evaluation
0.94
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