Issue 44, 2025

Synthesis of tetrahydropyrrolo[1,2-a]quinolinone analogues via CoCl2/AgSbF6-catalyzed cyclization of unactivated N,O-acetals with olefins

Abstract

A convenient method to access functionalized tetrahydropyrrolo[1,2-a]quinolinone skeletons has been achieved through a CoCl2/AgSbF6-catalyzed Povarov reaction of unactivated N-Ar N,O-acetals with styrene-type olefins. As a result, a series of 5-substituted tetrahydropyrrolo[1,2-a]quinolinone derivatives were conveniently obtained in moderate to good yields.

Graphical abstract: Synthesis of tetrahydropyrrolo[1,2-a]quinolinone analogues via CoCl2/AgSbF6-catalyzed cyclization of unactivated N,O-acetals with olefins

Supplementary files

Article information

Article type
Paper
Submitted
23 Aug 2025
Accepted
17 Oct 2025
First published
17 Oct 2025

Org. Biomol. Chem., 2025,23, 10200-10213

Synthesis of tetrahydropyrrolo[1,2-a]quinolinone analogues via CoCl2/AgSbF6-catalyzed cyclization of unactivated N,O-acetals with olefins

X. Li, Y. Zhang, Y. Zhang, C. Si, Q. Wang and B. Wei, Org. Biomol. Chem., 2025, 23, 10200 DOI: 10.1039/D5OB01374G

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