Issue 37, 2024

Formation of cyclopenta[c]quinolines through visible-light-induced photoredox cascade bis-annulations of 1,7-enynes with sulfoxonium ylides

Abstract

A novel visible-light-driven photoredox-catalyzed cascade bicyclization of 1,7-enynes with aqueous sulfoxonium ylides is reported. The reaction is highly chemoselective with three new C–C bonds, two new rings, and an all-carbon quaternary stereocenter constructed in a one-pot fashion. This mild protocol features a remarkably broad substrate scope with good functional group tolerance, providing a general and practical approach to access various cyclopenta[c]quinolines.

Graphical abstract: Formation of cyclopenta[c]quinolines through visible-light-induced photoredox cascade bis-annulations of 1,7-enynes with sulfoxonium ylides

Supplementary files

Article information

Article type
Communication
Submitted
04 Aug 2024
Accepted
27 Aug 2024
First published
28 Aug 2024

Org. Biomol. Chem., 2024,22, 7618-7622

Formation of cyclopenta[c]quinolines through visible-light-induced photoredox cascade bis-annulations of 1,7-enynes with sulfoxonium ylides

N. Xian, G. Deng and H. Huang, Org. Biomol. Chem., 2024, 22, 7618 DOI: 10.1039/D4OB01294A

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