Yayın: Synthesis of new aryl(hetaryl)-substituted tandospirone analogues with potential anxiolytic activity via reductive Heck type hydroarylations
| dc.contributor.author | Gunkara, Omer Tahir | |
| dc.contributor.author | Sucu, Bilgesu Onur | |
| dc.contributor.author | Ocal, Nuket | |
| dc.contributor.author | Kaufmann, Dieter E. | |
| dc.contributor.institutionauthor | GÜNKARA, Ömer Tahir | |
| dc.date.accessioned | 2026-06-27T13:22:19Z | |
| dc.date.issued | 2013 | |
| dc.description.abstract | Tandospirone (I), developed as an anxiolytic drug, is an aryl-piperazine compound that binds to both 5-HT1A and dopamine D4 receptors. Palladium-catalysed hydroarylation reactions of tandospirone analogues containing an oxygen bridge and 3-(trifluoromethyl)phenyl or 2,3-dichlorophenyl groups were studied in order to find a new stereoselective access to a series of new exo-aryl(hetaryl)-substituted derivatives with potential biological activity. | en |
| dc.description.sponsorship | Scientific and Technological Research Council of Turkey (TUBITAK) [109T380] | |
| dc.description.sponsorship | Yildiz Technical University Scientific Research Projects Coordination Department [2011-01-02-KAP03] | |
| dc.description.uri | https://doi.org/10.2478/s11696-013-0338-4 | |
| dc.identifier.doi | 10.2478/s11696-013-0338-4 | |
| dc.identifier.endpage | 649 | |
| dc.identifier.issn | 0366-6352 | |
| dc.identifier.issue | 6 | |
| dc.identifier.startpage | 643 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14981/52311 | |
| dc.identifier.volume | 67 | |
| dc.identifier.wos | 000316294900008 | |
| dc.language.iso | eng | |
| dc.publisher | VERSITA | |
| dc.relation.ispartof | CHEMICAL PAPERS | |
| dc.subject | tandospirone | |
| dc.subject | arylpiperazines | |
| dc.subject | C-C coupling | |
| dc.subject | hydroarylation | |
| dc.subject | heterocycles | |
| dc.subject | SUBSTITUTED TRICYCLIC IMIDES | |
| dc.subject | DOPAMINE D3 RECEPTOR | |
| dc.subject | UNSATURATED DICARBOXIMIDES | |
| dc.subject | PHARMACOLOGICAL AGENTS | |
| dc.subject | EPIBATIDINE | |
| dc.subject | DERIVATIVES | |
| dc.subject | CHEMISTRY | |
| dc.subject | AFFINITY | |
| dc.subject | NUCLEUS | |
| dc.subject | AGONIST | |
| dc.title | Synthesis of new aryl(hetaryl)-substituted tandospirone analogues with potential anxiolytic activity via reductive Heck type hydroarylations | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.import.source | WOS |