ArticleChemical science2026
Reductive rearrangement of substituted quinolines to 2,3-disubstituted indoles enabled by water activation.
Article in Chemical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Water, Alcohols, Amines, and Amides as Formal Hydrogen-Atom-Transfer Reagents Through Activation With Redox-Active Lewis Acids.Angewandte Chemie (International ed. in English) · 2026Review
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Herein, we report a selective reductive rearrangement of substituted quinolines into indoles-a privileged structural motif widely found in natural products and bioactive molecules. This quinoline skeletal editing is accomplished through water activation mediated by photocatalytically generated phosphine radical cations. The developed protocol provides a robust and broadly applicable approach for synthesizing diverse indole derivatives from readily available quinoline substrates.
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Registered trials
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