| dc.creator |
Cimen, Zeynep |
|
| dc.creator |
Akkoc, Senem |
|
| dc.creator |
KÖKBUDAK, ZÜLBİYE |
|
| dc.date |
2018-06-30T21:00:00Z |
|
| dc.date.accessioned |
2020-10-06T10:51:23Z |
|
| dc.date.available |
2020-10-06T10:51:23Z |
|
| dc.identifier |
a5c127c7-bd57-4f2a-92e5-fda31097044d |
|
| dc.identifier |
10.1002/hc.21458 |
|
| dc.identifier |
https://avesis.sdu.edu.tr/publication/details/a5c127c7-bd57-4f2a-92e5-fda31097044d/oai |
|
| dc.identifier.uri |
http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/68391 |
|
| dc.description |
1-Aminopyrimidine-2-one derivatives (1a-c) were prepared in two steps from furan-2,3-diones and semicarbazones in toluene/benzene. Pyrimidin-[1(2H)-yl] acetamide derivatives and isophthalimide derivatives were synthesized from the nucleophilic acyl substitution reactions of compounds 1a-c with chloroacetyl chloride. The structures of compounds 2a-f were verified by IR, H-1 NMR, C-13 NMR and elemental analyses. The obtained final organic compounds were tested as catalysts in the Mizoroki-Heck coupling reaction. They mostly exhibited very high catalytic activity results for the coupling reaction of styrene with different aryl bromide derivatives. |
|
| dc.language |
eng |
|
| dc.rights |
info:eu-repo/semantics/closedAccess |
|
| dc.title |
Reactions of aminopyrimidine derivatives with chloroacetyl and isophthaloyl chlorides |
|
| dc.type |
info:eu-repo/semantics/article |
|