| dc.creator |
AKTAŞ, AYDIN |
|
| dc.creator |
Akkoc, Senem |
|
| dc.creator |
GÖK, YETKİN |
|
| dc.date |
2013-07-31T21:00:00Z |
|
| dc.date.accessioned |
2020-10-06T09:25:03Z |
|
| dc.date.available |
2020-10-06T09:25:03Z |
|
| dc.identifier |
1018cd1b-f2b5-4b9a-8993-a941e716069d |
|
| dc.identifier |
10.1080/00958972.2013.819092 |
|
| dc.identifier |
https://avesis.sdu.edu.tr/publication/details/1018cd1b-f2b5-4b9a-8993-a941e716069d/oai |
|
| dc.identifier.uri |
http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/53481 |
|
| dc.description |
Naphthalenomethyl-substituted imidazolidinium salts (1a-g) were prepared and characterized by conventional spectroscopic methods, H-1 NMR, C-13 NMR, FTIR, and elemental analysis techniques. The in situ prepared three component systems naphthalenomethyl-substituted imidazolidinium salts, Pd(OAc)(2), and K2CO3 catalyzed quantitatively the Mizoroki-Heck and Suzuki-Miyaura coupling of aryl halides under mild conditions in aqueous media. |
|
| dc.language |
eng |
|
| dc.rights |
info:eu-repo/semantics/closedAccess |
|
| dc.title |
Palladium catalyzed Mizoroki-Heck and Suzuki-Miyaura reactions using naphthalenomethyl-substituted imidazolidin-2-ylidene ligands in aqueous media |
|
| dc.type |
info:eu-repo/semantics/article |
|