Synthesis of tetraaminoalkenes containing the reduced pyrimidine skeleton and the x-ray molecular structure of 1,1'-ethylene-3,3'-dibenzylbi(hexahydropyrimidin-2-ylidene)
dc.authorid | Cetinkaya, Bekir/0000-0002-4551-8650 | |
dc.authorid | Tahir, Dr. Muhammad Nawaz/0000-0002-6815-9806 | |
dc.contributor.author | Alici, B | |
dc.contributor.author | Cetinkaya, E | |
dc.contributor.author | Cetinkaya, B | |
dc.contributor.author | Ulku, D | |
dc.contributor.author | Tahir, MN | |
dc.date.accessioned | 2024-08-04T21:01:17Z | |
dc.date.available | 2024-08-04T21:01:17Z | |
dc.date.issued | 1996 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | Deprotonation of a 1,1'-bridged bis(1,3-diaikyl-1,4,5,6-tetrahydropyrimidinium) diiodide with NaH gives in high yield a tetraaminoalkene 4, whereas the corresponding non-bridged tetrahydropyrimidinium iodide reacts with NaH only in the presence of KOBu; the title bridged tetraaminoalkene 4f was structurally characterized by single-crystal X-ray diffraction. | en_US |
dc.identifier.endpage | 517 | en_US |
dc.identifier.issn | 0308-2342 | |
dc.identifier.issue | 12 | en_US |
dc.identifier.startpage | 516 | en_US |
dc.identifier.uri | https://hdl.handle.net/11616/104249 | |
dc.identifier.wos | WOS:A1996WF14200005 | en_US |
dc.identifier.wosquality | N/A | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.language.iso | en | en_US |
dc.publisher | Royal Soc Chemistry | en_US |
dc.relation.ispartof | Journal of Chemical Research-S | 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 | Coordination Chemistry | en_US |
dc.subject | Carbene | en_US |
dc.subject | Enetetramines | en_US |
dc.subject | Complexes | en_US |
dc.title | Synthesis of tetraaminoalkenes containing the reduced pyrimidine skeleton and the x-ray molecular structure of 1,1'-ethylene-3,3'-dibenzylbi(hexahydropyrimidin-2-ylidene) | en_US |
dc.type | Article | en_US |