Synthesis of 5-(hydroxy-, chloro-, bromomethyl)furan-2-enones Based on Fructose and their Antioxidant Activity

Sakhautdinova, G.F.; Malikova, R.N.; Bortsova, Y.L.; Mochalov, K.S.; Muratov, E.M.; Galimova, E.F.; Sakhautdinov, I.M.; Mustafin, A.G.

Synthesis of 5-(hydroxy-, chloro-, bromomethyl)furan-2-enones Based on Fructose and their Antioxidant Activity

Sakhautdinova, G.F., Malikova, R.N., Bortsova, Y.L., Mochalov, K.S., Muratov, E.M., Galimova, E.F., Sakhautdinov, I.M., Mustafin, A.G.

Publication date: 2021

DOI: 10.1007/s10600-021-03500-0

Abstract:

New enones were synthesized from 5-hydroxymethylfurfurol (5-HMF) and its derivatives using Wittig reactions of various phosphoranes. The synthesized enones were observed to affect free-radical oxidation in model systems, in particular, to suppress generation of reactive oxygen species. © 2021, Springer Science+Business Media, LLC, part of Springer Nature.

Keywords:
5-hydroxymethylfurfurol, antioxidant activity, enones, imides, phosphoranes, phosphorus ylides, Wittig reaction, Scopus, Web of Science

Издатель: Springer

Тип: Article

Synthesis of 5-(hydroxy-, chloro-, bromomethyl)furan-2-enones Based on Fructose and their Antioxidant Activity

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