In situ generated 1-alkylbenzimidazole-palladium catalyst for the Suzuki coupling of aryl chlorides
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, cilt.234, sa.1-2, ss.181-185, 2005 (SCI-Expanded)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 234 Sayı: 1-2
- Basım Tarihi: 2005
- Doi Numarası: 10.1016/j.molcata.2005.02.031
- Dergi Adı: JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED)
- Sayfa Sayıları: ss.181-185
- Anahtar Kelimeler: palladium, benzimidazole ligands, C-C coupling, Suzuki reaction, PALLADIUM CATALYSTS, MIYAURA REACTION, C-C, COMPLEXES, LIGANDS, AMINATION, BROMIDES, HECK, DERIVATIVES, CHEMISTRY
- İnönü Üniversitesi Adresli: Evet
Özet
Six 1-alkylbenzimidazole have been prepared and characterized by conventional spectroscopic methods and elemental analyses. Novel in situ generated palladium-benzimidazole complexes, tested in the Suzuki coupling reaction between phenylboronic acid and several aryl chlorides showed excellent catalytic activity. (c) 2005 Elsevier B.V. All rights reserved.