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Synthesis and inhibiting activity of pyrocatechol monoethers
Abstract O-Alkylation of pyrocatechol with 4-chloromethyl-1,3-dioxolane has been investigated. The ether formation selectivity is largely determined by the structure of the reactants and the conditions of the process. The inhibiting effect of the synthesized ortho-substituted phenols has been examined in the model system of radical chain oxidation of 1,4-dioxane.
Synthesis and inhibiting activity of pyrocatechol monoethers
Abstract O-Alkylation of pyrocatechol with 4-chloromethyl-1,3-dioxolane has been investigated. The ether formation selectivity is largely determined by the structure of the reactants and the conditions of the process. The inhibiting effect of the synthesized ortho-substituted phenols has been examined in the model system of radical chain oxidation of 1,4-dioxane.
Synthesis and inhibiting activity of pyrocatechol monoethers
Timofeeva, S. A. (Autor:in) / Yakupova, L. R. (Autor:in) / Safiullin, R. L. (Autor:in) / Zlotskii, S. S. (Autor:in)
Petroleum Chemistry ; 52 ; 432-436
01.11.2012
5 pages
Aufsatz (Zeitschrift)
Elektronische Ressource
Englisch
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