Abstract:
A new versatile access to azido-substituted N-alkylnitramines is based on ring opening in N-nitrooxazolidines and N-nitroperhydro-1,3-oxazines with thionyl chloride followed by treatment with sodium azide. Representative N,N-bis(azidoalkyl)- and N-azidoalkyl-N-methoxymethyl- containing nitramines were synthesized and characterized.
Citation:
D. B. Vinogradov, P. V. Bulatov, E. Yu. Petrov, V. A. Tartakovsky, “New access to azido-substituted alkylnitramines”, Mendeleev Commun., 31:6 (2021), 795–796
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https://www.mathnet.ru/eng/mendc1045
https://www.mathnet.ru/eng/mendc/v31/i6/p795
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