Chemoselective Suzuki-Miyaura cross-coupling reactions of methyl 4-bromo-3-(trifluoromethylsulfonyloxy)-2-naphthoate

Zien Khaddour, Nadi Eleya, Omer A. Akrawi, Aws M. Hamdy, T. Patonay, Alexander Villinger, Peter Langer

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Arylated naphthalenes were prepared by Suzuki-Miyaura cross-coupling reactions of methyl 4-bromo-3-(trifluoromethylsulfonyloxy)-2-naphthoate. The reactions proceeded with very good chemoselectivity in favor of the triflate group, due to additive electronic ortho electronic effects.

Original languageEnglish
Pages (from-to)5201-5203
Number of pages3
JournalTetrahedron Letters
Volume54
Issue number38
DOIs
Publication statusPublished - Sep 18 2013

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Naphthalenes
Cross Reactions

Keywords

  • Catalysis
  • Chemoselectivity
  • Naphthalene
  • Palladium
  • Suzuki-Miyaura reaction

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Chemoselective Suzuki-Miyaura cross-coupling reactions of methyl 4-bromo-3-(trifluoromethylsulfonyloxy)-2-naphthoate. / Khaddour, Zien; Eleya, Nadi; Akrawi, Omer A.; Hamdy, Aws M.; Patonay, T.; Villinger, Alexander; Langer, Peter.

In: Tetrahedron Letters, Vol. 54, No. 38, 18.09.2013, p. 5201-5203.

Research output: Contribution to journalArticle

Khaddour, Zien ; Eleya, Nadi ; Akrawi, Omer A. ; Hamdy, Aws M. ; Patonay, T. ; Villinger, Alexander ; Langer, Peter. / Chemoselective Suzuki-Miyaura cross-coupling reactions of methyl 4-bromo-3-(trifluoromethylsulfonyloxy)-2-naphthoate. In: Tetrahedron Letters. 2013 ; Vol. 54, No. 38. pp. 5201-5203.
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AU - Eleya, Nadi

AU - Akrawi, Omer A.

AU - Hamdy, Aws M.

AU - Patonay, T.

AU - Villinger, Alexander

AU - Langer, Peter

PY - 2013/9/18

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KW - Palladium

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