| dc.contributor.author |
Alici, B |
|
| dc.contributor.author |
Ozdemir, I |
|
| dc.contributor.author |
Gurbuz, N |
|
| dc.contributor.author |
Cetinkaya, E |
|
| dc.contributor.author |
Cetinkaya, B |
|
| dc.date.accessioned |
2022-10-19T12:10:29Z |
|
| dc.date.available |
2022-10-19T12:10:29Z |
|
| dc.date.issued |
2005 |
|
| dc.identifier.uri |
http://hdl.handle.net/11616/83775 |
|
| dc.description.abstract |
Four functionalized bis(1,4,5,6-tetrahyropyrimidinium) salts (2a-d) have been prepared and characterized by conventional spectroscopic methods and elemental analyses. 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 Pd(OAC)(2) / bis(1,4,5,6-tetrahyropyrimidinium) bromides (2a-d) and CS2CO3 catalyses quantitatively the Suzuki cross-coupling of deactivated aryl chloride. |
|
| 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 |
HETEROCYCLES |
|
| dc.title |
1,4,5,6-tetrahyropyrimidinium halides ligands for Suzuki-Miyaura |
|
| dc.title |
cross-coupling of unactivated aryl chlorides |
|