Regioselective Suzuki-Miyaura cross-coupling reactions of 4-methyl-6,7-bis(trifluoromethanesulfonyloxy)coumarin

Aws M. Hamdy, Nadi Eleya, Hamid H. Mohammed, Zien Khaddour, T. Patonay, Alexander Villinger, Peter Langer

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Arylated coumarins were prepared by site-selective Suzuki-Miyaura cross-coupling reaction of the bis(triflate) of 4-methyl-6,7-dihydroxycoumarin.

Original languageEnglish
Pages (from-to)3568-3571
Number of pages4
JournalTetrahedron Letters
Volume54
Issue number27
DOIs
Publication statusPublished - Jul 3 2013

Fingerprint

Coumarins
Cross Reactions
esculetin
methyl triflate
coumarin

Keywords

  • Catalysis
  • Coumarin
  • Palladium
  • Regioselectivity
  • Suzuki-Miyaura reaction

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Regioselective Suzuki-Miyaura cross-coupling reactions of 4-methyl-6,7-bis(trifluoromethanesulfonyloxy)coumarin. / Hamdy, Aws M.; Eleya, Nadi; Mohammed, Hamid H.; Khaddour, Zien; Patonay, T.; Villinger, Alexander; Langer, Peter.

In: Tetrahedron Letters, Vol. 54, No. 27, 03.07.2013, p. 3568-3571.

Research output: Contribution to journalArticle

Hamdy, Aws M. ; Eleya, Nadi ; Mohammed, Hamid H. ; Khaddour, Zien ; Patonay, T. ; Villinger, Alexander ; Langer, Peter. / Regioselective Suzuki-Miyaura cross-coupling reactions of 4-methyl-6,7-bis(trifluoromethanesulfonyloxy)coumarin. In: Tetrahedron Letters. 2013 ; Vol. 54, No. 27. pp. 3568-3571.
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AU - Mohammed, Hamid H.

AU - Khaddour, Zien

AU - Patonay, T.

AU - Villinger, Alexander

AU - Langer, Peter

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