Abstract
Homolytic reactions of 2-ethoxy-1,3-oxathiolane in the presence of benzoyl peroxide and tert-butyl peroxide in chlorobenzene have been studied. The principal reaction products are diethyl monothiocarbonate and 1,3-oxathiolane-2-one. The yields and ratios of the products are temperature-dependent.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 919–920, July, 1985.
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Taganliev, A., Rol'nik, L.Z., Pastushenko, E.V. et al. Free-radical reactions of 2-ethoxy-1,3-oxathiolane. Chem Heterocycl Compd 21, 761–762 (1985). https://doi.org/10.1007/BF00519141
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DOI: https://doi.org/10.1007/BF00519141