Indole ring expansion into quinolines with TMSCCl3/TMSCBr3

Abstract

Reactivity adaptation speciation perceives reactants as a dynamic supply pool of shifting reactive units for opportunistic reactivity-matching diverse-manifold pathways to varied reactivity patterns, revealing the title C2[double bond, length as m-dash]C3–CCl/CBr insertion ring expansion of indole into quinoline, N1–H–TMS nucleophilic substitution, and N1–H–CCl3 nucleophilic substitution for the indole–TMSCCl3/TMSCBr3 reactions.

Graphical abstract: Indole ring expansion into quinolines with TMSCCl3/TMSCBr3

Supplementary files

Article information

Article type
Communication
Submitted
29 Aug 2025
Accepted
15 Sep 2025
First published
23 Sep 2025

Chem. Commun., 2025, Advance Article

Indole ring expansion into quinolines with TMSCCl3/TMSCBr3

Z. Wang, H. Xu, X. Han and J. Zhu, Chem. Commun., 2025, Advance Article , DOI: 10.1039/D5CC04994F

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