Nitrolysis of 3-substituted 1,5-dinitro-1,3,5-triazepanes

Nitrolysis of 3-substituted 1,5-dinitro-1,3,5-triazepanes Full article

Journal

Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285

Output data

Year: 2025, Volume: 74, Number: 11, Pages: 3506-3516 Pages count : 11 DOI: 10.1007/s11172-025-4825-x

Authors

Gribov P.S. ¹ , Frank D.F. ¹ , Vinogradova I.D. ¹ , Malkina D.A. ¹ , Nazarova A.A. ¹ , Suponitsky K.Yu. ¹ , Sheremetev A.B. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation

A general method was developed for the nitrolysis of 3-R-1,5-dinitro-1,3,5-triazepanes, which is accompanied by the triazepane ring opening and N-nitration, to form linear nitramines as 1-acetoxy-2,5,7-trinitro-2,5,7-triazaoctane derivatives. The structures of these compounds were characterized by spectroscopic methods.

Gribov P.S. , Frank D.F. , Vinogradova I.D. , Malkina D.A. , Nazarova A.A. , Suponitsky K.Y. , Sheremetev A.B.
Nitrolysis of 3-substituted 1,5-dinitro-1,3,5-triazepanes
Russian Chemical Bulletin. 2025. V.74. N11. P.3506-3516. DOI: 10.1007/s11172-025-4825-x WOS Scopus OpenAlex

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