| dc.contributor.author |
Ozdemir, I |
|
| dc.contributor.author |
Demir, S |
|
| dc.contributor.author |
Yasar, S |
|
| dc.contributor.author |
Cetinkaya, B |
|
| dc.date.accessioned |
2022-10-19T12:10:28Z |
|
| dc.date.available |
2022-10-19T12:10:28Z |
|
| dc.date.issued |
2005 |
|
| dc.identifier.uri |
http://hdl.handle.net/11616/83755 |
|
| dc.description.abstract |
A highly effective, easy to handle and environmentally benign process for palladium-mediated Suzuki cross-coupling is developed. The in situ prepared three-component system Pd(OAC)(2)-1,3bis(alkyl)imidazolinium chlorides (2a-f) and CS2CO3 catalyses quantitatively the Suzuki crosscoupling of deactivated aryl chlorides. Copyright (C) 2004 John Wiley Sons, Ltd. |
|
| dc.description.abstract |
C1 Inonu Univ, Fac Sci & Arts, Dept Chem, TR-44280 Malatya, Turkey. |
|
| dc.description.abstract |
Ege Univ, Dept Chem, TR-35100 Izmir, Turkey. |
|
| dc.source |
APPLIED ORGANOMETALLIC CHEMISTRY |
|
| dc.title |
Palladium-catalysed Suzuki reaction of aryl chlorides in aqueous media |
|
| dc.title |
using 1,3-dialkylimidazolidin-2-ylidene ligands |
|