I. V. Ovchinnikov, K. A. Lyssenko, N. N. Makhova, “An unexpected transformation of 3,4-bis(isocyanato)furoxan into 3,3’-bi(1,2,4-oxadiazol-5-one)”, Mendeleev Commun., 19:3 (2009), 144

Эта публикация цитируется в следующих 16 статьяx:

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Shuangfei Zhu, Wei Yang, Qiang Gan, Changgen Feng, “Initial Steps and Thermochemistry of Unimolecular Decomposition of Oxadiazole Energetic Materials: Quantum Chemistry Modeling”, J. Phys. Chem. A, 125:36 (2021), 7929
Teng Fei, Chenghui Sun, Chunlin He, Siping Pang, “A comparative study of bridged 1,2,4-oxazolones and their derivatives”, Energetic Materials Frontiers, 1:1 (2020), 26
Dmitry Khakimov, Victor Zelenov, Nikita Baraboshkin, Tatyana Pivina, “The unusual combination of beauty and power of furoxano-1,2,3,4-tetrazine 1,3-dioxides: a theoretical study of crystal structures”, J Mol Model, 25:4 (2019)
Teng Fei, Yao Du, Siping Pang, “Synthesis, Crystal Structure, and Thermal Behavior of a Novel Insensitive Energetic Cocrystal Composed of 3,3′‐Bis(1,2,4‐oxadiazole)‐5,5′‐dione and 4‐Amino‐1,2,4‐triazole”, Zeitschrift anorg allge chemie, 644:10 (2018), 466
Qiong Yu, Guangbin Cheng, Xuehai Ju, Chunxu Lu, Qiuhan Lin, Hongwei Yang, “Compounds based on 3-amino-4-(5-methyl-1,2,4-oxadiazol-3-yl)furazan as insensitive energetic materials”, New J. Chem., 41:3 (2017), 1202
Hao Wei, Chunlin He, Jiaheng Zhang, Jean'ne M. Shreeve, “Combination of 1,2,4‐Oxadiazole and 1,2,5‐Oxadiazole Moieties for the Generation of High‐Performance Energetic Materials”, Angew Chem Int Ed, 54:32 (2015), 9367
Hao Wei, Chunlin He, Jiaheng Zhang, Jean'ne M. Shreeve, “Combination of 1,2,4‐Oxadiazole and 1,2,5‐Oxadiazole Moieties for the Generation of High‐Performance Energetic Materials”, Angewandte Chemie, 127:32 (2015), 9499
Marcos A. Kettner, Konstantin Karaghiosoff, Thomas M. Klapötke, Muhamed Sućeska, Swetlana Wunder, “3,3′‐Bi(1,2,4‐oxadiazoles) Featuring the Fluorodinitromethyl and Trinitromethyl Groups”, Chemistry A European J, 20:25 (2014), 7622
Bakr F. Abdel‐Wahab, Hanan A. Mohamed, Rizk E. Khidre, Mohamed F. El‐Mansy, “An Overview of the Literature on the Synthetic Routes to Azolyloxadiazoles”, Journal of Heterocyclic Chem, 51:5 (2014), 1215
Н. Н. Махова, А. С. Куликов, “Успехи химии моноциклических амино- и нитрофуроксанов”, Усп. хим., 82:11 (2013), 1007–1033 ; N. N. Makhova, A. S. Kulikov, “Advances in the chemistry of monocyclic amino- and nitrofuroxans”, Russian Chem. Reviews, 82:11 (2013), 1007–1033
Nina N. Makhova, Igor V. Ovchinnikov, Alexandr S. Kulikov, Dmitriy V. Khakimov, Marina S. Molchanova, Tatyana S. Pivina, “Diaminofuroxan: Synthetic Approaches and Computer‐Aided Study of Thermodynamic Stability”, Propellants Explo Pyrotec, 37:5 (2012), 549
Zhanda Fu, Rui Su, Yang Wang, Yao‐Feng Wang, Wei Zeng, Nan Xiao, Yukai Wu, Zhiming Zhou, Jun Chen, Fu‐Xue Chen, “Synthesis and Characterization of Energetic 3‐Nitro‐1,2,4‐oxadiazoles”, Chemistry A European J, 18:7 (2012), 1886
Igor V. Ovchinnikov, Konstantin A. Lyssenko, Nina N. Makhova, “ChemInform Abstract: An Unexpected Transformation of 3,4‐Bis(isocyanato)furoxan into 3,3′‐Bi(1,2,4‐oxadiazol‐5‐one).”, ChemInform, 40:42 (2009)