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Mendeleev Communications, 2022, Volume 32, Issue 3, Pages 349–350
DOI: https://doi.org/10.1016/j.mencom.2022.05.019 (Mi mendc660) 		 
Communications

Nitration of benzyl derivatives of acetylated hexaazaisowurtzitane

D. A. Kulagina, A. S. Goryaev, I. N. Chernyshov, S. V. Sysolyatin

Institute for Problems of Chemical & Energetic Technologies, Siberian Branch of the Russian Academy of Sciences, Biysk, Russian Federation
Full-text PDF (146 kB) Supplementary materials
DOI: https://doi.org/10.1016/j.mencom.2022.05.019
Abstract: Nitration of N-benzylated 2,4,6,8,10,12-hexaazaisowurtzitane derivatives occurs selectively at para-positions of the benzyl groups. The best reagent for this reaction is ammonium nitrate in sulfuric acid.
Keywords: hexaazaisowurtzitanes, cage compounds, nitration, nitrating mixtures, benzyl groups, selective reaction.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (566.6 Kb)


Citation: D. A. Kulagina, A. S. Goryaev, I. N. Chernyshov, S. V. Sysolyatin, “Nitration of benzyl derivatives of acetylated hexaazaisowurtzitane”, Mendeleev Commun., 32:3 (2022), 349–350
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