In-situ generated functionalized benzimidazol-2-ylidene-palladium catalyst for Suzuki reaction
Küçük Resim Yok
Tarih
2004
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Polish Chemical Soc
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
From readily available starting materials functionalized 1,3-dialkylbenzimidazolium salts (la-g) have been prepared and characterized by conventional spectroscopic methods and elemental analysis. The in situ prepared three component system Pd(OAC)(2)/1,3-dialkylbenzimidazolium halides (1a-g) and Cs2CO3 catalyses Suzuki cross-coupling of aryl chloride substrates. These concepts for making catalysts in situ open the way for the discovery of many new catalysts via the interaction of commercially available metal complexes and suitable electron releasing ligands.
Açıklama
Anahtar Kelimeler
Suzuki, functional carbene, aryl chlorides, phenylboronic acid
Kaynak
Polish Journal of Chemistry
WoS Q Değeri
Q3
Scopus Q Değeri
N/A
Cilt
78
Sayı
11-12
