Abstract
Hydroxylamine hydrochloride efficiently reduces peroxide products of olefins ozonolysis into carbonyl compounds. Depending on the substrate character, solvent, and the treatment conditions the arising aldehydes transformed along the route aldehyde→aldoxime→nitrile→ester into individual compounds or their mixtures, or give the corresponding acetals.
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Original Russian Text © G.Yu. Ishmuratov, A.Kh. Shayakhmetova, M.P. Yakovleva, Yu.V. Legostaeva, O.V. Shitikova, E.G. Galkin, G.A. Tolstikov, 2007, published in Zhurnal Organicheskoi Khimii, 2007, Vol. 43, No. 8, pp. 1125–1129.
For Communication LXVII, see [1].
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Ishmuratov, G.Y., Shayakhmetova, A.K., Yakovleva, M.P. et al. Ozonolysis of alkenes and study of reactions of polyfunctional compounds: LXVIII. Investigation of transformations of peroxide products of olefins ozonolysis treated with hydroxylamine hydrochloride. Russ J Org Chem 43, 1114–1119 (2007). https://doi.org/10.1134/S1070428007080039
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DOI: https://doi.org/10.1134/S1070428007080039