Silver-catalyzed synthesis of polyfunctionalized 1,7- and 2,7-benzonaphthyridine scaffolds and access to perlolidine derivatives

Abstract

A regio- and chemoselective silver-catalyzed one-pot synthesis of benzo[b][1,7]- and benzo[c][2,7]-naphthyridines has been developed via a sequential Michael addition and silver-mediated cyclization strategy. The protocol exhibits excellent selectivity, high yields, and broad functional group tolerance. The resulting polyfunctionalized benzo[c][2,7]-naphthyridine scaffolds were further investigated as key intermediates toward the synthesis of perlolidine analogues, highlighting their potential for the discovery of novel bioactive compounds and alkaloid frameworks.

Graphical abstract: Silver-catalyzed synthesis of polyfunctionalized 1,7- and 2,7-benzonaphthyridine scaffolds and access to perlolidine derivatives

Supplementary files

Article information

Article type
Paper
Submitted
01 Sep 2025
Accepted
06 Oct 2025
First published
08 Oct 2025

Org. Biomol. Chem., 2025, Advance Article

Silver-catalyzed synthesis of polyfunctionalized 1,7- and 2,7-benzonaphthyridine scaffolds and access to perlolidine derivatives

K. Vashishtha, K. Chahal, N. Bhoi, D. Tomy, B. Sridhar, M. Alla and K. R. Reddy, Org. Biomol. Chem., 2025, Advance Article , DOI: 10.1039/D5OB01410G

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