Biginelli Dihydropyrimidines: A Tunable Class of Alkyl Radical Precursors

Abstract

Alkyl-substituted dihydropyrimidines (DHPyms), synthesised via the Biginelli reaction, are introduced as tunable alternatives to 4-alkyl Hantzsch Dihydropyridines (DHPs) in radical chemistry. Leveraging the modularity of the Biginelli reaction, we systematically explored the redox properties, UV/vis absorption, and synthetic potential of DHPyms in radical-mediated transformations, identifying dimethylamino-substituted DHPym as a highly reactive, bench-stable, and easily synthesised alkyl radical precursor.

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Article information

Article type
Edge Article
Submitted
14 Jan 2026
Accepted
12 Mar 2026
First published
13 Mar 2026
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2026, Accepted Manuscript

Biginelli Dihydropyrimidines: A Tunable Class of Alkyl Radical Precursors

S. Ratnam, S. Unone, N. Alia, E. D. Hafeneger and D. Janssen-Müller, Chem. Sci., 2026, Accepted Manuscript , DOI: 10.1039/D6SC00376A

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