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Efficient synthesis of N-carboxyalkyl-substituted dithiaza- and dioxadithiazacycloalkanes by cyclocondensation of amino acids with formaldehyde and α,ω-dithiols

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Abstract

A method of synthesis of N-carboxyalkyl-substituted dithiaza- and dioxadithiazacycloalkanes was developed consisting in a tricomponent [1+2+1]-cyclocondensation of amino acids with formaldehyde and aliphatic α,ω-dithiols (1,3-propane-, 1,4-butanedithiols, 3,6-dioxa-1,8-octanedithiol).

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Correspondence to G. R. Khabibullina.

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Original Russian Text © G.R. Khabibullina, Е.S. Fedotova, М.F. Abdullin, Т.V. Tyumkina, V.R. Akhmetova, A.G. Ibragimov, 2017, published in Zhurnal Organicheskoi Khimii, 2017, Vol. 53, No. 2, pp. 277–281.

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Khabibullina, G.R., Fedotova, E.S., Abdullin, M.F. et al. Efficient synthesis of N-carboxyalkyl-substituted dithiaza- and dioxadithiazacycloalkanes by cyclocondensation of amino acids with formaldehyde and α,ω-dithiols. Russ J Org Chem 53, 277–281 (2017). https://doi.org/10.1134/S1070428017020233

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  • DOI: https://doi.org/10.1134/S1070428017020233

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