Visible light-promoted cascade synthesis of pyrazolidinones <i>via N</i>-aryl glycine and azomethine imines

We present an effective, visible light-driven method for the synthesis of <i>N</i>-(β-amino)pyrazolidin-3-ones from <i>N</i>-aryl glycine and azomethine imines. This additive-free protocol utilizes blue light (<i>λ</i><sub>max</sub> = 435-445 nm) at room temperature, enabling a radical-mediated cascade reaction that delivers a diverse range of pyrazolidinones in yields up to 99%. The mild conditions, high efficiency, and broad substrate scope of this process make it an attractive strategy for streamlined synthesis in drug discovery and material science.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob00497g
Citations
1
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.94
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article

Visible light-promoted cascade synthesis of pyrazolidinones via N-aryl glycine and azomethine imines

Ganesh Udari, Surya Prakash Singh, Balasubramanian Sridhar
1 citations
Organic & Biomolecular Chemistry
Sulfur-Based Synthesis Techniques
0.94
article

Visible light-promoted cascade synthesis of pyrazolidinones via N-aryl glycine and azomethine imines

Ganesh Udari, Surya Prakash Singh, Balasubramanian Sridhar
article en
1 citations

Abstract

We present an effective, visible light-driven method for the synthesis of <i>N</i>-(β-amino)pyrazolidin-3-ones from <i>N</i>-aryl glycine and azomethine imines. This additive-free protocol utilizes blue light (<i>λ</i><sub>max</sub> = 435-445 nm) at room temperature, enabling a radical-mediated cascade reaction that delivers a diverse range of pyrazolidinones in yields up to 99%. The mild conditions, high efficiency, and broad substrate scope of this process make it an attractive strategy for streamlined synthesis in drug discovery and material science.

Organic & Biomolecular ChemistryVol. 23(19)
Indian Institute of Chemical Technology (IN), Academy of Scientific and Innovative Research (IN)
Openalex Percentile: Top 28%
Sulfur-Based Synthesis Techniques
0.94
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