Yıldırım, Ayhan2024-08-012024-08-012015-03-010022-152Xhttps://doi.org/10.1002/jhet.2091https://onlinelibrary.wiley.com/doi/10.1002/jhet.2091https://hdl.handle.net/11452/43632A series of novel cationic surfactants bearing 1,3,4-oxadiazole and tetraazatricyclic ring structures were synthesized by alkyl chain elongation of 5-{10-[4-(hydroxymethyl)phenoxy]decyl}-2,3-dihydro-1,3,4-oxadiazole-2-thione with homologous series of alkyl bromides, followed by chlorination of the corresponding benzyl alcohols with thionyl chloride and quaternization of the obtained intermediates with hexamethylenetetramine.eninfo:eu-repo/semantics/closedAccessGene deliveryIn-vitroCorrosion-inhibitorsGemini surfactantsCarbon-steelLipidsVivoAlkylationCyclization134-oxadiazoleLipidsAlkylationCyclization134-oxadiazoleLipidsScience & technologyPhysical sciencesChemistry, organicChemistrySynthesis of novel alkyl-sulfanyl 1,3,4-oxadiazolyl-1,3,5,7-tetraazatricyclic ammonium chloride type cationic surfactantsArticle00035162620003152252652210.1002/jhet.20911943-5193