| dc.contributor.author |
Ozdemir, I |
|
| dc.contributor.author |
Yasar, S |
|
| dc.contributor.author |
Demir, S |
|
| 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/11616/83768 |
|
| dc.description.abstract |
From readily available starting materials, six 1,3-dialkly-imidazolinium bromides (2a-f) have been prepared and characterized by conventional spectroscopic methods and elemental analyses. The incorporation of saturated N-heterocyclic carbenes into palladium precatalysts gives high catalyst activity in the Suzuki coupling of deactivated aryl chloride substrates in aqueous media. The complexes were generated in the presence of Pd(OAC)(2) by in situ deprotonation of 2a-f. (c) 2005 Wiley Periodicals, Inc. |
|
| dc.description.abstract |
C1 Inonu Univ, Dept Chem, Fac Sci & Art, TR-44280 Malatya, Turkey. |
|
| dc.description.abstract |
Ege Univ, Dept Chem, Fac Sci, TR-35100 Bornova, Turkey. |
|
| dc.source |
HETEROATOM CHEMISTRY |
|
| dc.title |
Suzuki reaction of aryl chlorides using saturated N-heterocarbene |
|
| dc.title |
ligands |
|