Heck and suzuki reactions of aryl halides catalyzed by 1,3-dialkylimidazolinium/palladium

YAŞAR S., Oezdemir I., Cetinkaya B.

CHINESE JOURNAL OF CATALYSIS, cilt.29, sa.2, ss.185-190, 2008 (SCI-Expanded, Scopus) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 29 Sayı: 2
  • Basım Tarihi: 2008
  • Doi Numarası: 10.1016/s1872-2067(08)60023-6
  • Dergi Adı: CHINESE JOURNAL OF CATALYSIS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.185-190
  • Anahtar Kelimeler: Heck reaction, suzuki reaction, aryl halide, imidazolinium salt, palladium, carbene, CROSS-COUPLING REACTIONS, N-HETEROCARBENE LIGANDS, HETEROCYCLIC CARBENE LIGANDS, TRANSITION-METAL-COMPLEXES, AQUEOUS-MEDIA, EFFICIENT CATALYSTS, PALLADIUM CATALYSTS, ARYLBORONIC ACIDS, MIYAURA REACTION, C-C
  • İnönü Üniversitesi Adresli: Evet

Özet

New, sterically demanding 1,3-dialkylimidazolinium salts used as N-heterocyclic carbene precursors were synthesized and characterized. These salts, combined with palladium acetate, provided active catalysts for Heck and suzuki cross-coupling of aryl chlorides and bromides under mild conditions.