Chemoselective Suzuki-Miyaura reactions of 4-trifluoromethylsulfonyloxy-6- bromocoumarin

Omer A. Akrawi, Gerg Z. Nagy, T. Patonay, Alexander Villinger, Peter Langer

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

Suzuki-Miyaura reactions of 4-trifluoromethylsulfonyloxy-6-bromocoumarin provide a convenient access to arylated coumarins. The reactions proceed with excellent chemoselectivity in favour of position 4.

Original languageEnglish
Pages (from-to)3206-3209
Number of pages4
JournalTetrahedron Letters
Volume53
Issue number26
DOIs
Publication statusPublished - Jun 27 2012

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Coumarins

Keywords

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

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Chemoselective Suzuki-Miyaura reactions of 4-trifluoromethylsulfonyloxy-6- bromocoumarin. / Akrawi, Omer A.; Nagy, Gerg Z.; Patonay, T.; Villinger, Alexander; Langer, Peter.

In: Tetrahedron Letters, Vol. 53, No. 26, 27.06.2012, p. 3206-3209.

Research output: Contribution to journalArticle

Akrawi, Omer A. ; Nagy, Gerg Z. ; Patonay, T. ; Villinger, Alexander ; Langer, Peter. / Chemoselective Suzuki-Miyaura reactions of 4-trifluoromethylsulfonyloxy-6- bromocoumarin. In: Tetrahedron Letters. 2012 ; Vol. 53, No. 26. pp. 3206-3209.
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