Аннотация:
Oxidation of ethyl cyanoglyoxylate 2-oxime followed by KOH treatment affords stable potassium salt of nitroacetonitrile which is a reliable substitute of hazardous free nitroacetonitrile in organic synthesis.
Образец цитирования:
E. K. Voinkov, E. N. Ulomsky, V. L. Rusinov, K. V. Savateev, V. V. Fedotov, E. B. Gorbunov, M. L. Isenov, O. S. Eltsov, “New stable form of nitroacetonitrile”, Mendeleev Commun., 26:2 (2016), 172–173
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2150
https://www.mathnet.ru/rus/mendc/v26/i2/p172
Эта публикация цитируется в следующих 17 статьяx:
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I. I. Butorin, O. A. Konovalova, P. A. Slepukhin, S. K. Kotovskaya, V. L. Rusinov, “An alternative synthesis of 7-amino-6-nitro-substituted azolo[1,5-a]pyrimidines”, Mendeleev Commun., 34:5 (2024), 706–708
R. I. Baichurin, A. V. Fel'gendler, L. V. Baichurina, O. B. Vuks, “Nitroacetonitrile in Reactions with Enones”, Russ J Gen Chem, 94:12 (2024), 3196
E. V. Bersneva, E. K. Voinkov, R. A. Drokin, N. A. Gerasimova, N. P. Evstigneeva, N. V. Zilberberg, N. V. Kungurov, V. L. Rusinov, “Synthesis and study of antimicrobial activity of 4-amino-1,2,4-triazolo[5,1-c][1,2,4]triazine derivatives against Neisseria gonorrhoeae”, Russ Chem Bull, 72:12 (2023), 3013
Д. Н. Ляпустин, В. В. Федотов, Е. Н. Уломский, В. Л. Русинов, О. Н. Чупахин, “Последние достижения в химии двухуглеродных нитросодержащих синтетических эквивалентов”, Усп. хим., 92:4 (2023), RCR5077 ; D. N. Lyapustin, V. V. Fedotov, E. N. Ulomsky, V. L. Rusinov, O. N. Chupakhin, “Recent advances in the chemistry of two-carbon nitro-containing synthetic equivalents”, Russian Chem. Reviews, 92:4 (2023), RCR5077
Egor K. Voinkov, Roman A. Drokin, Victor V. Fedotov, Ilya I. Butorin, Konstantin V. Savateev, Daniil N. Lyapustin, Denis A. Gazizov, Evgeny B. Gorbunov, Pavel A. Slepukhin, Natalya A. Gerasimova, Natalya P. Evstigneeva, Natalya V. Zilberberg, Nikolay V. Kungurov, Evgeny N. Ulomsky, Vladimir L. Rusinov, “Azolo[5,1‐c][1,2,4]triazines and Azoloazapurines: Synthesis, Antimicrobial activity and in silico Studies”, ChemistrySelect, 7:5 (2022)
Kento Iwai, Nagatoshi Nishiwaki, “Nitroacetonitrile and Its Synthetic Equivalents”, J. Org. Chem., 86:19 (2021), 13177
Kejia Li, Wei Huang, Ziwei An, Xiangshuai Wei, Yongxing Tang, “Efficient Synthesis of a Superior Heat-Resistant Energetic Material Based on Fused Pyrazolotriazine Ring”, Crystal Growth & Design, 21:12 (2021), 6872
Shannon E. Creegan, Matthias Zeller, Edward F. C. Byrd, Davin G. Piercey, “Synthesis and Characterization of the Energetic 3‐Azido‐5‐amino‐6‐nitro‐1,2,4‐triazine”, Propellants Explo Pyrotec, 46:2 (2021), 214
Shannon E. Creegan, Davin G. Piercey, “Nitroacetonitrile as a versatile precursor in energetic materials synthesis”, RSC Adv., 10:65 (2020), 39478
V. L. Rusinov, V. N. Charushin, O. N. Chupakhin, “Biologically active azolo-1,2,4-triazines and azolopyrimidines”, Russ Chem Bull, 67:4 (2018), 573
Christopher J. Snyder, Thomas W. Myers, Gregory H. Imler, David E. Chavez, Damon A. Parrish, Jacqueline M. Veauthier, R. Jason Scharff, “Tetrazolyl Triazolotriazine: A New Insensitive High Explosive”, Prop., Explos., Pyrotech., 42:3 (2017), 238
E. K. Voinkov, E. N. Ulomsky, V. L. Rusinov, R. A. Drokin, V. V. Fedotov, E. B. Gorbunov, “1-Morpholino-2-nitroethylene as a precursor of nitroacetaldehyde in the synthesis of azolo[5,1-c][1,2,4]triazines”, Mendeleev Commun., 27:3 (2017), 285–286
Davin G. Piercey, David E. Chavez, Brian L. Scott, Greg H. Imler, Damon A. Parrish, “An Energetic Triazolo‐1,2,4‐Triazine and its N‐Oxide”, Angew Chem Int Ed, 55:49 (2016), 15315
Davin G. Piercey, David E. Chavez, Brian L. Scott, Greg H. Imler, Damon A. Parrish, “An Energetic Triazolo‐1,2,4‐Triazine and its N‐Oxide”, Angewandte Chemie, 128:49 (2016), 15541
Egor K. Voinkov, Evgeny N. Ulomskiy, Vladimir L. Rusinov, Konstantin V. Savateev, Victor V. Fedotov, Evgeny B. Gorbunov, Maksim L. Isenov, Oleg S. Eltsov, “ChemInform Abstract: New Stable Form of Nitroacetonitrile.”, ChemInform, 47:32 (2016)
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