Turkish Journal of Chemistry
DOI
10.3906/kim-1701-42
Abstract
1-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.
Keywords
Hydrazines, hydrazones, ABTS, antioxidant capacities, biological properties
First Page
306
Last Page
316
Recommended Citation
KIVRAK, ARİF; YILMAZ, CAN; KONUŞ, METİN; KOCA, HALİL; AYDEMİR, SELAHATTİN; and OAGAZ, JEGER ALI
(2018)
"Synthesis and biological properties of novel1-methyl-2-(2-(prop-2-yn-1-yloxy)benzylidene) hydrazine analogues,"
Turkish Journal of Chemistry: Vol. 42:
No.
2, Article 9.
https://doi.org/10.3906/kim-1701-42
Available at:
https://journals.tubitak.gov.tr/chem/vol42/iss2/9