Gold-Catalysed N-Allenamide Cyclisation as a Platform for the Construction of Indole-Fused Quinoxaline and Quinoline Scaffolds

Abstract

We report a gold-catalysed cyclisation of N-allenamides derived from 1- and 2-(2-aminoaryl)indoles, providing easy access to 5,6-dihydroindolo[1,2-a]quinoxalines and 6,11-dihydro-5H-indolo[3,2-c]quinolines. The reaction proceeds under mild conditions, tolerates diverse functional groups, and enables the synthesis of previously unexplored indole-fused heterocycles, whose versatility was demonstrated through selected post-functionalisation reactions.

Supplementary files

Article information

Article type
Paper
Submitted
27 Nov 2025
Accepted
12 Jan 2026
First published
13 Jan 2026
This article is Open Access
Creative Commons BY-NC license

Org. Biomol. Chem., 2025, Accepted Manuscript

Gold-Catalysed N-Allenamide Cyclisation as a Platform for the Construction of Indole-Fused Quinoxaline and Quinoline Scaffolds

S. Meraviglia, M. Goudarzi, S. Borsi, G. Abbiati and V. Pirovano, Org. Biomol. Chem., 2025, Accepted Manuscript , DOI: 10.1039/D5OB01867F

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