Unver, HalilBiyikoglu, MutluhanBulut, Adnan2020-06-252020-06-252013Unver, H., Biyikoglu, M., & Bulut, A. (2013). Non-Acidic Mediated Friedel-Craft Reaction of Thiophene Using EtAlCl2. Asian Journal of Chemistry, 25(15), 8772–8774.0970-70770975-427Xhttps://doi.org/10.14233/ajchem.2013.15607https://hdl.handle.net/20.500.12587/5432Since 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 %).eninfo:eu-repo/semantics/openAccessThiopheneAcylationAlkyl Lewis acidElectrophilic aromatic substitutionArticle25158772877410.14233/ajchem.2013.156072-s2.0-84886621689Q4WOS:000325204200122Q4