Site-selective Suzuki-Miyaura reactions of 2,6-dichlorobenzoxazole

Aws M. Hamdy, Nadi Eleya, Hamid H. Mohammed, Tamás Patonay, Anke Spannenberg, Peter Langer

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Suzuki-Miyaura reactions of 2,6-dichlorobenzoxazole provide a convenient access to arylated benzoxazoles. The reactions proceed with excellent site-selectivity in favour of position 2, due to electronic reasons.

Original languageEnglish
Pages (from-to)2081-2086
Number of pages6
JournalTetrahedron
Volume69
Issue number8
DOIs
Publication statusPublished - Feb 25 2013

Keywords

  • Benzoxazole
  • Catalysis
  • Palladium
  • Site-selectivity
  • Suzuki-Miyaura reaction

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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  • Cite this

    Hamdy, A. M., Eleya, N., Mohammed, H. H., Patonay, T., Spannenberg, A., & Langer, P. (2013). Site-selective Suzuki-Miyaura reactions of 2,6-dichlorobenzoxazole. Tetrahedron, 69(8), 2081-2086. https://doi.org/10.1016/j.tet.2012.11.021