Regioselective palladium(0)-catalyzed cross-coupling reactions of 5,7-dichloro-1,6-naphthyridine

Iftikhar Ali, Zahid Hassan, Martin Hein, Abiodun Falodun, Tamás Patonay, Alexander Villinger, Peter Langer

Research output: Contribution to journalArticle

7 Citations (Scopus)


A variety of mono- and diarylated naphthyridine derivatives were prepared by site-selective Suzuki-Miyaura cross-coupling reactions of 5,7-dichloro-1,6-naphthyridine. The first attack occurs at position 5.

Original languageEnglish
Article numberSS-2012-N0111-OP
Pages (from-to)2255-2263
Number of pages9
JournalSynthesis (Germany)
Issue number14
Publication statusPublished - Jun 29 2012



  • Suzuki reaction
  • catalysis
  • naphthyridine
  • palladium
  • regioselectivity

ASJC Scopus subject areas

  • Catalysis
  • Organic Chemistry

Cite this

Ali, I., Hassan, Z., Hein, M., Falodun, A., Patonay, T., Villinger, A., & Langer, P. (2012). Regioselective palladium(0)-catalyzed cross-coupling reactions of 5,7-dichloro-1,6-naphthyridine. Synthesis (Germany), 44(14), 2255-2263. [SS-2012-N0111-OP].