A Beneficial Effect of Ortho-Substituents In the Arylation of (Benzene)Tricarbonylmanganese(1+) Hexafluorophosphate(1-)
dc.contributor.author | Astley, Dk | |
dc.contributor.author | Astley, St | |
dc.date.accessioned | 2019-10-27T11:35:05Z | |
dc.date.available | 2019-10-27T11:35:05Z | |
dc.date.issued | 1995 | |
dc.department | Ege Üniversitesi | en_US |
dc.description.abstract | ortho-Substituted aryllithium and aryl Grignard reagents react with (benzene)manganesetricarbonyl cation (1) to give good yields of the expected ring adducts. The presence of the ortho substituent(s) appears to be necessary for the satisfactory outcome of the reaction with aryllithiums. This reactivity opens up the possibility of preparing novel heterocyclic structures via the initial reaction of 1 with functionalised metallated arenes. | en_US |
dc.identifier.doi | 10.1016/0022-328X(94)05085-P | |
dc.identifier.endpage | 255 | en_US |
dc.identifier.issn | 0022-328X | |
dc.identifier.issn | 0022-328X | en_US |
dc.identifier.issue | 01.Feb | en_US |
dc.identifier.startpage | 253 | en_US |
dc.identifier.uri | https://doi.org/10.1016/0022-328X(94)05085-P | |
dc.identifier.uri | https://hdl.handle.net/11454/33629 | |
dc.identifier.volume | 487 | en_US |
dc.identifier.wos | WOS:A1995QD55700037 | en_US |
dc.identifier.wosquality | N/A | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier Science Sa Lausanne | en_US |
dc.relation.ispartof | Journal of Organometallic Chemistry | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | MANGANESE | en_US |
dc.subject | CARBONYL | en_US |
dc.subject | ARENE COMPLEXES | en_US |
dc.subject | ORTHOMETALLATION | en_US |
dc.subject | METAL CARBONYL CATIONS | en_US |
dc.title | A Beneficial Effect of Ortho-Substituents In the Arylation of (Benzene)Tricarbonylmanganese(1+) Hexafluorophosphate(1-) | en_US |
dc.type | Article | en_US |