| dc.creator |
Akkoc, Senem |
|
| dc.creator |
İLHAN, İLHAN ÖZER |
|
| dc.creator |
GÖK, YETKİN |
|
| dc.creator |
Kayser, Veysel |
|
| dc.date |
2017-04-30T21:00:00Z |
|
| dc.date.accessioned |
2020-10-06T09:36:29Z |
|
| dc.date.available |
2020-10-06T09:36:29Z |
|
| dc.identifier |
2d9fc0d1-fded-4823-9a17-9fc155fff0c8 |
|
| dc.identifier |
10.1016/j.ica.2017.01.025 |
|
| dc.identifier |
https://avesis.sdu.edu.tr/publication/details/2d9fc0d1-fded-4823-9a17-9fc155fff0c8/oai |
|
| dc.identifier.uri |
http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/56417 |
|
| dc.description |
Five new palladium complexes were efficiently synthesized from the reaction of benzimidazolium salts, potassium carbonate (K2CO3) and palladium chloride (PdCl2) in pyridine (for 3-5) or 3-chloropyridine (for 6 and 7). The synthesized complexes were characterized and tested in Suzuki-Miyaura cross-coupling reaction as catalysts. In the presence of catalysts 3-7, biaryl products were obtained in moderate yields when phenylboronic acid was used as boronic acid derivative. However, the coupling of thianaphthene-2-boronic acid with 1-chloro-4-nitrobenzene generated low yields although a longer period of time was used in comparison to the coupling of phenylboronic acid with aryl chlorides. (C) 2017 Elsevier B.V. All rights reserved. |
|
| dc.language |
eng |
|
| dc.rights |
info:eu-repo/semantics/closedAccess |
|
| dc.title |
Carbon-carbon bond formation catalyzed by PEPPSI Pd-NHC |
|
| dc.type |
info:eu-repo/semantics/article |
|