Yayın: Reductive Heck Reactions and [3+2] Cycloadditions of Unsaturated N,N'-Bistricyclic Imides
| dc.contributor.author | Gul, Melek | |
| dc.contributor.author | Kulu, Irem | |
| dc.contributor.author | Gunkara, Omer Tahir | |
| dc.contributor.author | Ocal, Nuket | |
| dc.contributor.institutionauthor | GÜNKARA, Ömer Tahir | |
| dc.date.accessioned | 2026-06-27T13:22:09Z | |
| dc.date.issued | 2013 | |
| dc.description.abstract | The C-C coupling of N,N'-bis(5-norbornene-2,3-dicarboximide) (3) and N,N'-bis(7-oxa-5-norbornene-2,3-dicarboximide) (6) with aryl and heteroaryl iodides gave under reductive Heck conditions the C-aryl(hetaryl), substituted N,N'bistricyclic imides 7a-f and 8a,b. The fused spiro-1,3-indandionolylpyrrolidine compounds, 9, 10 and 11 were also obtained from ninhydrine, sarcosine and 3 or 6 via [3+2] cycloaddition. | en |
| dc.description.sponsorship | Yildiz Technical University Scientific Research Projects Coordination Department [2011-01-02-KAP03] | |
| dc.identifier.eissn | 1580-3155 | |
| dc.identifier.endpage | 94 | |
| dc.identifier.issn | 1318-0207 | |
| dc.identifier.issue | 1 | |
| dc.identifier.pubmed | 23841336 | |
| dc.identifier.startpage | 87 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14981/52279 | |
| dc.identifier.volume | 60 | |
| dc.identifier.wos | 000317014600012 | |
| dc.language.iso | eng | |
| dc.publisher | SLOVENSKO KEMIJSKO DRUSTVO | |
| dc.relation.ispartof | ACTA CHIMICA SLOVENICA | |
| dc.subject | Alkenes | |
| dc.subject | cycloadditions | |
| dc.subject | heterocycles | |
| dc.subject | hydroarylations | |
| dc.subject | triyclic imides | |
| dc.subject | SUBSTITUTED CYCLIC IMIDES | |
| dc.subject | HYDROARYLATION | |
| dc.subject | EPIBOXIDINE | |
| dc.subject | ANALOGS | |
| dc.subject | DICARBOXIMIDES | |
| dc.subject | ANTICANCER | |
| dc.subject | Chemistry | |
| dc.title | Reductive Heck Reactions and [3+2] Cycloadditions of Unsaturated N,N'-Bistricyclic Imides | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.import.source | WOS |