Abstract
A method was developed for the preparation of amino derivatives of 1,3-dioxanes of the furan series by amalgam reduction of the corresponding nitro compounds. This method makes it possible to obtain amino compounds without destruction of the furan and dioxane rings. 2-α′-Aminofuryl-5-alkyl-5-methylol- and 5-α′-aminofuryl-5,5-bis(chloromethyl)-1,3-dioxanes and their azomethines were synthesized for the first time.
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See [5] for communication III.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 440–442, April, 1971.
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Zelikman, Z.I., Soltovets, G.N., Kul'nevich, V.G. et al. Furan acetal compounds. Chem Heterocycl Compd 7, 410–411 (1971). https://doi.org/10.1007/BF00471472
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DOI: https://doi.org/10.1007/BF00471472