| dc.contributor.author |
Ozdemir, I |
|
| dc.contributor.author |
Gok, Y |
|
| dc.contributor.author |
Gurbuz, N |
|
| dc.contributor.author |
Cetinkaya, E |
|
| dc.contributor.author |
Cetinkaya, B |
|
| dc.date.accessioned |
2022-10-19T12:13:21Z |
|
| dc.date.available |
2022-10-19T12:13:21Z |
|
| dc.date.issued |
2004 |
|
| dc.identifier.uri |
http://hdl.handle.net/11616/84122 |
|
| dc.description.abstract |
Four functionalized bis(benzimidazolium) salts (2a-d) have been prepared and characterized by conventional spectroscopic methods and elemental analyses. A highly effective, easy to handle, and environmentally bengin process for palladium-mediated Suzuki cross-coupling was developed. The in situ prepared three-component system Pd(OAc)(2)/bis(benzimidazolium) bromides (2a-d) and Cs2CO3 catalyzes quantitatively the Suzuki cross-coupling of deactivated aryl chloride in aqueous media. |
|
| dc.description.abstract |
C1 Inonu Univ, Dept Chem, TR-44069 Malatya, Turkey. |
|
| dc.description.abstract |
Ege Univ, Dept Chem, Bornova, Turkey. |
|
| dc.source |
SYNTHETIC COMMUNICATIONS |
|
| dc.title |
Suzuki-Miyaura reaction of unactivated aryl chlorides using |
|
| dc.title |
benzimidazol-2-ylidene ligands |
|