| dc.contributor.author |
Ozdemir, I |
|
| dc.contributor.author |
Gurbuz, N |
|
| dc.contributor.author |
Gok, Y |
|
| dc.contributor.author |
Cetinkaya, E |
|
| dc.contributor.author |
Cetinkaya, B |
|
| dc.date.accessioned |
2022-10-19T12:10:36Z |
|
| dc.date.available |
2022-10-19T12:10:36Z |
|
| dc.date.issued |
2005 |
|
| dc.identifier.uri |
http://hdl.handle.net/11616/83853 |
|
| dc.description.abstract |
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 of Pd(OAc)(2), 1,3-dialkyltetrahydrodiazepinium chlorides (2a-e), and K2CO3 catalyzes quantitatively the Suzuki-Miyaura 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 |
SYNLETT |
|
| dc.title |
Palladium-catalyzed Suzuki-Miyaura reaction of aryl chlorides in aqueous |
|
| dc.title |
media using tetrahydrodiazepinium salts as carbene ligands |
|