Chemoselective Suzuki-Miyaura cross-coupling reactions of 6-bromo-3-(trifluoromethylsulfonyloxy)flavone

Omer A. Akrawi, T. Patonay, Krisztina Kónya, Peter Langer

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Arylated flavones were prepared by Suzuki-Miyaura reactions of 6-bromo-3-(trifluoro-sulfonyloxy)flavone. The reactions proceeded with very good chemoselectivity in favor of position 3.

Original languageEnglish
Article numberST-2013-D0046-L
Pages (from-to)860-864
Number of pages5
JournalSynlett
Volume24
Issue number7
DOIs
Publication statusPublished - 2013

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Keywords

  • catalysis
  • cross-coupling reactions
  • flavones
  • heterocycles
  • palladium

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Chemoselective Suzuki-Miyaura cross-coupling reactions of 6-bromo-3-(trifluoromethylsulfonyloxy)flavone. / Akrawi, Omer A.; Patonay, T.; Kónya, Krisztina; Langer, Peter.

In: Synlett, Vol. 24, No. 7, ST-2013-D0046-L, 2013, p. 860-864.

Research output: Contribution to journalArticle

Akrawi, Omer A. ; Patonay, T. ; Kónya, Krisztina ; Langer, Peter. / Chemoselective Suzuki-Miyaura cross-coupling reactions of 6-bromo-3-(trifluoromethylsulfonyloxy)flavone. In: Synlett. 2013 ; Vol. 24, No. 7. pp. 860-864.
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KW - palladium

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