| dc.contributor.author | Unver, Halil | |
| dc.contributor.author | Biyikoglu, Mutluhan | |
| dc.contributor.author | Bulut, Adnan | |
| dc.date.accessioned | 2020-06-25T18:06:59Z | |
| dc.date.available | 2020-06-25T18:06:59Z | |
| dc.date.issued | 2013 | |
| dc.identifier.citation | Unver, H., Biyikoglu, M., & Bulut, A. (2013). Non-Acidic Mediated Friedel-Craft Reaction of Thiophene Using EtAlCl2. Asian Journal of Chemistry, 25(15), 8772–8774. | en_US |
| dc.identifier.issn | 0970-7077 | |
| dc.identifier.issn | 0975-427X | |
| dc.identifier.uri | https://doi.org/10.14233/ajchem.2013.15607 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12587/5432 | |
| dc.description | WOS: 000325204200122 | en_US |
| dc.description.abstract | Since alkyl Lewis acids are Bronsted bases, they give a non-acidic reaction media. In this context, acylation of thiophene is investigated in the presence of EtAlCl2 and non-acidic media. Besides 8 examples of thiophene, one example for pyrrole is synthesized in moderate to high yields (up to 99 %). | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Asian Journal Of Chemistry | en_US |
| dc.relation.isversionof | 10.14233/ajchem.2013.15607 | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Thiophene | en_US |
| dc.subject | Acylation | en_US |
| dc.subject | Alkyl Lewis acid | en_US |
| dc.subject | Electrophilic aromatic substitution | en_US |
| dc.title | Non-Acidic Mediated Friedel-Craft Reaction of Thiophene Using EtAlCl2 | en_US |
| dc.type | article | en_US |
| dc.contributor.department | Kırıkkale Üniversitesi | en_US |
| dc.identifier.volume | 25 | en_US |
| dc.identifier.issue | 15 | en_US |
| dc.identifier.startpage | 8772 | en_US |
| dc.identifier.endpage | 8774 | en_US |
| dc.relation.journal | Asian Journal Of Chemistry | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
