Kivrak, ArifYilmaz, CanKonus, MetinKoca, HalilAydemir, SelahattinOagaz, Jeger Ali2025-05-102025-05-1020181300-052710.3906/kim-1701-422-s2.0-85048041741https://doi.org/10.3906/kim-1701-42https://hdl.handle.net/20.500.14720/7574Kivrak, Arif/0000-0003-4770-2686; Konus, Metin/0000-0002-9953-1375; Yilmaz, Can/0000-0002-0028-66141-Methyl-2-(2-(prop-2-yn-1-yloxy)benzylidene)hydrazine analogues were readily prepared in good yields by the reaction of 2-(prop-2-yn-1-yloxy)benzaldehydes and methyl hydrazine. The reaction tolerates a variety of substituents on the 2-hydroxybenzaldehyde to form nitro-, halo-, methoxy-, and naphthyl-substituted 1-methyl-2-(2-(prop-2-yn-1-yloxy)benzylidene)hydrazines. The in vitro antioxidant capacity measurements revealed that among all the analyzed hydrazine analogues that surpassed the Trolox standard, 1-(2-(but-3-ynyl)-5-nitrobenzylidene)-2-methylhydrazine had the maximum value, which was approximately 1.7 times that of Trolox.eninfo:eu-repo/semantics/openAccessHydrazinesHydrazonesAbtsAntioxidant CapacitiesBiological PropertiesArticle422Q4Q3306316WOS:000431245300009