One-Pot Cross-Coupling/C–H Functionalization Reactions: Quinoline as a Substrate and Ligand through N–Pd Interaction

Herein, we report a one-pot process that marries mechanistically distinct, traditional cross-coupling reactions with C–H functionalization using the same precatalyst. The reactions proceed in yields of up to 95%, in air, and require no extraneous ligand. The reactions are thought to be facilitated b...

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Veröffentlicht in:Journal of organic chemistry 2020-02, Vol.85 (4), p.2585-2596
Hauptverfasser: Shanahan, Rachel M, Hickey, Aobha, Bateman, Lorraine M, Light, Mark E, McGlacken, Gerard P
Format: Artikel
Sprache:eng
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Zusammenfassung:Herein, we report a one-pot process that marries mechanistically distinct, traditional cross-coupling reactions with C–H functionalization using the same precatalyst. The reactions proceed in yields of up to 95%, in air, and require no extraneous ligand. The reactions are thought to be facilitated by harnessing the substrate quinoline as an N-ligand, and evidence of the palladium–quinoline interaction is provided by 1H-15N HMBC NMR spectroscopy and X-ray crystallographic structures. Application of the methodology is demonstrated by the quick formation of fluorescent, π-extended frameworks.
ISSN:0022-3263
1520-6904
DOI:10.1021/acs.joc.9b03321