Heck and suzuki reactions of aryl halides catalyzed by 1,3-dialkylimidazolinium/palladium
CHINESE JOURNAL OF CATALYSIS, cilt.29, sa.2, ss.185-190, 2008 (SCI-Expanded, Scopus)
- 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.