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dc.contributor.authorSarac, K. and Orek, C. and Cetin, A. and Dastan, T. and Koparir, P. and Dastan, S.D. and Koparir, M.
dc.date.accessioned2021-04-08T12:08:54Z
dc.date.available2021-04-08T12:08:54Z
dc.date.issued2016
dc.identifier10.1080/10426507.2016.1192620
dc.identifier.issn10426507
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84978538788&doi=10.1080%2f10426507.2016.1192620&partnerID=40&md5=c15da8cb887d45ee6af2c1b7c3dfd129
dc.identifier.urihttp://acikerisim.bingol.edu.tr/handle/20.500.12898/4717
dc.description.abstractDiamines were added to arylaldehydes in ethanol, which resulted in corresponding diimines. Novel bis-1-aminophosphinic acid compounds were synthesized through the interaction of diimines and hypophosphorous acid. The new compounds were characterized by elemental analyses, FT-IR and1H,13C and31P NMR techniques. The in vitro antioxidant activity of the newly synthesized compounds were measured and found to exhibit significantly higher antioxidant activity than the standard. © 2016 Taylor & Francis Group, LLC.
dc.language.isoEnglish
dc.sourcePhosphorus, Sulfur and Silicon and the Related Elements
dc.titleSynthesis and in vitro antioxidant evaluation of new bis(α-aminoalkyl)phosphinic acid derivatives


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