Palladium-catalyzed Suzuki-Miyaura reaction of aryl chlorides in aqueous media using tetrahydrodiazepinium salts as carbene ligands
Küçük Resim Yok
Tarih
2005
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Georg Thieme Verlag Kg
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
A highly effective, easy to handle, and environmentally benign process for palladium-mediated Suzuki cross-coupling was developed. The in situ prepared three-component system of Pd(OAc)(2), 1,3-dialkyltetrahydrodiazepinium chlorides (2a-e), and K2CO3 catalyzes quantitatively the Suzuki-Miyaura cross-coupling of deactivated aryl chloride.
Açıklama
Anahtar Kelimeler
tetrahydrodiazepinium, Suzuki-Miyaura reaction, palladium, C-C coupling, N-heterocyclic carbene
Kaynak
Synlett
WoS Q Değeri
Q1
Scopus Q Değeri
Q2
Cilt
Sayı
15
