Abstract:
The reactions of 3-amino-4-R-furazans with CCl4 in the presence of AlCl3 or [bmim][AlCl4] gave the corresponding (3-R-furazan-4-yl)dichloroimines in preparatively useful yields
Document Type:
Article
Language: English
Citation:
A. B. Sheremetev, N. S. Aleksandrova, I. L. Yudin, “A new strategy for the functionalization of aminofurazans: the synthesis of (3-R-furazan-4-yl)dichloroimines”, Mendeleev Commun., 13:1 (2003), 31–33
Linking options:
https://www.mathnet.ru/eng/mendc3943
https://www.mathnet.ru/eng/mendc/v13/i1/p31
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Nadezhda V. Palysaeva, Aleksei G. Gladyshkin, Irina A. Vatsadze, Kyrill Yu. Suponitsky, Dmitry E. Dmitriev, Aleksei B. Sheremetev, “N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design”, Org. Chem. Front., 6:2 (2019), 249
Ilya V. Kuchurov, Mikhail N. Zharkov, Leonid L. Fershtat, Nina N. Makhova, Sergey G. Zlotin, “Prospective Symbiosis of Green Chemistry and Energetic Materials”, ChemSusChem, 10:20 (2017), 3914
Ewies F. Ewies, Marwa El-Hussieny, Naglaa F. El-Sayed, Mamdouh M. Ali, Abeer E. Mahmoud, “Synthesis, characterization, and antitumor evaluation of 4-aminoximidofurazan derivatives”, Phosphorus, Sulfur, and Silicon and the Related Elements, 191:7 (2016), 1000
A. B. Sheremetev, N. S. Aleksandrova, K. Yu. Suponitsky, M. Yu. Antipin, V. A. Tartakovsky, “One-pot synthesis of 4,6,8-trinitro-4,5,7,8-tetrahydro-6H-furazano[3,4-f]-1,3,5-triazepine in ionic liquids”, Mendeleev Commun., 20:5 (2010), 249–252
G. Nikonov, S. Bobrov, Comprehensive Heterocyclic Chemistry III, 2008, 315
Aleksei B. Sherementev, Natal'ya S. Aleksandrova, Igor L. Yudin, “A New Strategy for the Functionalization of Aminofurazans: The Synthesis of (3‐R‐Furazan‐4‐yl)dichloroimines.”, ChemInform, 34:31 (2003)
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