4.7 Article

Two Consecutive Palladium(II)-Promoted C-H Alkenylation Reactions for the Synthesis of 3-Alkenylquinolones

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 357, Issue 2-3, Pages 463-473

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201400931

Keywords

C-C coupling; C-H activation; oxidative Heck reaction; palladium; quinolones

Funding

  1. Ministerio de Economia y Competitividad [CTQ2013-41229-P]
  2. Gobierno Vasco [IT-623-13]
  3. Universidad del Pais Vasco/Euskal Herriko Unibertsitatea UPV/EHU [UFI11/22, PPM12/03]
  4. Gobierno Vasco

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Highly substituted quinolones are obtained through an efficient and atom economical procedure that involves two consecutive palladium(II)-catalyzed C-H alkenylation reactions. A selective 6-endo intramolecular C-H alkenylation leads to 4-substituted quinolones that have been further functional-ized at C-3 through a second intermolecular C-H alkenylation reaction.

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