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

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

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

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
Volume44
Issue number14
DOIs
Publication statusPublished - 2012

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Naphthyridines
Palladium
Derivatives

Keywords

  • catalysis
  • naphthyridine
  • palladium
  • regioselectivity
  • Suzuki reaction

ASJC Scopus subject areas

  • Organic Chemistry
  • Catalysis

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, 44(14), 2255-2263. [SS-2012-N0111-OP]. https://doi.org/10.1055/s-0032-1316540

Regioselective palladium(0)-catalyzed cross-coupling reactions of 5,7-dichloro-1,6-naphthyridine. / Ali, Iftikhar; Hassan, Zahid; Hein, Martin; Falodun, Abiodun; Patonay, T.; Villinger, Alexander; Langer, Peter.

In: Synthesis, Vol. 44, No. 14, SS-2012-N0111-OP, 2012, p. 2255-2263.

Research output: Contribution to journalArticle

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, vol. 44, no. 14, SS-2012-N0111-OP, pp. 2255-2263. https://doi.org/10.1055/s-0032-1316540
Ali, Iftikhar ; Hassan, Zahid ; Hein, Martin ; Falodun, Abiodun ; Patonay, T. ; Villinger, Alexander ; Langer, Peter. / Regioselective palladium(0)-catalyzed cross-coupling reactions of 5,7-dichloro-1,6-naphthyridine. In: Synthesis. 2012 ; Vol. 44, No. 14. pp. 2255-2263.
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