Issue 19, 2025

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

Abstract

We present an effective, visible light-driven method for the synthesis of N-(β-amino)pyrazolidin-3-ones from N-aryl glycine and azomethine imines. This additive-free protocol utilizes blue light (λmax = 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.

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

Supplementary files

Article information

Article type
Communication
Submitted
24 mar 2025
Accepted
01 apr 2025
First published
02 apr 2025

Org. Biomol. Chem., 2025,23, 4666-4670

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

G. Udari, A. Jansi Rani, B. Sridhar and S. P. Singh, Org. Biomol. Chem., 2025, 23, 4666 DOI: 10.1039/D5OB00497G

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