Silver-catalyzed diastereoselective cascade radical cyclization of CF3-alkenyl quinolones with diarylphosphine oxides

Abstract

A silver catalyzed phosphorus radical promoted cascade cyclization of quinolone derived unactivated olefins is described to access dual-functionalized dihydrophenanthridinones bearing phosphoryl and CF3-carbinol groups. The reaction achieves concurrent C–P and C–C bond formation in one step, providing excellent yields and high diastereoselectivity (>20 : 1). The CF3 group exerts a strong steric effect, which helps achieve remarkable diastereoselectivity.

Graphical abstract: Silver-catalyzed diastereoselective cascade radical cyclization of CF3-alkenyl quinolones with diarylphosphine oxides

Supplementary files

Article information

Article type
Communication
Submitted
18 Sep 2025
Accepted
24 Oct 2025
First published
28 Oct 2025

Org. Biomol. Chem., 2025, Advance Article

Silver-catalyzed diastereoselective cascade radical cyclization of CF3-alkenyl quinolones with diarylphosphine oxides

J. Prudhviraj, C. Nagababu, R. Sateesh, K. S. Desireddy and N. Punna, Org. Biomol. Chem., 2025, Advance Article , DOI: 10.1039/D5OB01505G

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