Yayın: Hydroarylation of bicyclic, unsaturated dicarboximides: access to aryl-substituted, bridged perhydroisoindoles
| dc.contributor.author | Goksu, Goekce | |
| dc.contributor.author | Gul, Melek | |
| dc.contributor.author | Ocal, Nueket | |
| dc.contributor.author | Kaufmann, Dieter E. | |
| dc.date.accessioned | 2026-06-27T13:08:45Z | |
| dc.date.issued | 2008 | |
| dc.description.abstract | The C-C coupling of the two bicyclic, unsaturated dicarboximides 6 and 8 with aryl and hetaryl halides gave under reductive Heck conditions the 5-substituted N-phenylbicyclo[2.2.1]heptane-2,3-dicarboxim ides 7 and 9. Reduction of these imides opens a new access to the bridged perhydroisoindole derivatives 12 and 14 with prospective biological activity. (c) 2008 Elsevier Ltd. All rights reserved. | en |
| dc.description.uri | https://doi.org/10.1016/j.tetlet.2008.02.171 | |
| dc.identifier.doi | 10.1016/j.tetlet.2008.02.171 | |
| dc.identifier.eissn | 1873-3581 | |
| dc.identifier.endpage | 2688 | |
| dc.identifier.issn | 0040-4039 | |
| dc.identifier.issue | 17 | |
| dc.identifier.startpage | 2685 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14981/50352 | |
| dc.identifier.volume | 49 | |
| dc.identifier.wos | 000255270500003 | |
| dc.language.iso | eng | |
| dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | |
| dc.relation.ispartof | TETRAHEDRON LETTERS | |
| dc.subject | palladium | |
| dc.subject | homogenous catalysis | |
| dc.subject | C-C coupling | |
| dc.subject | reduction | |
| dc.subject | amine | |
| dc.subject | aromatics | |
| dc.subject | PALLADIUM-CATALYZED REACTIONS | |
| dc.subject | DOMINO-HECK REACTIONS | |
| dc.subject | CYCLIC IMIDES | |
| dc.subject | EPIBATIDINE | |
| dc.subject | AMINES | |
| dc.subject | Chemistry | |
| dc.title | Hydroarylation of bicyclic, unsaturated dicarboximides: access to aryl-substituted, bridged perhydroisoindoles | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.import.source | WOS |