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Information × Registration Number 2198U000030, Article popup.category Стаття Title popup.author popup.publication 01-01-1998 popup.source_user Сумський державний університет popup.source http://essuir.sumdu.edu.ua/handle/123456789/2275 popup.publisher Издательство СумГУ Description The row of di- and tetrahydrothiophendioxyde derivatives was synthesysed and in model experiments their antioxydative features in comparisson with the etalon antioxydant - -tocopherol acetate was studied. It was founded out that the compounds which paralelly with sulfolanil group has the fourth-in-row nitrogene atom, are the most antioxydantaly active. Besides this, N-(3-piperidinosulfolanil-4) N-methylpiperidinium monomethylsulfate and [2-(3-sulfolaniloxy) aethyl] trimethylammonii iodide in their activity are 1.5-1.8 times better than -tocopherol acetate. The obtanuation of the un-known salts of triaminosulfolane and tridimethylaminosulfolane with the succinate acid and N-(3-Piperidinosulfonil-4) N-methylpiperidinium-monomethylsulfate is described in the article. When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/2275 popup.nrat_date 2025-03-24 Close