Abstract:
Thermal recyclization of the 3-diazenofuroxanyl unit to form the 4-nitro-1,2,3-triazole fragment has been found in noncondensed 1,2,5-oxadiazol 2-oxide derivatives (3,3’-azofuroxans) with acetamido substituents in the 4,4’-positions.
Document Type:
Article
Language: English
Citation:
N. N. Makhova, A. N. Blinnikov, “New version of mononuclear heterocyclic rearrangement”, Mendeleev Commun., 9:1 (1999), 17–19
Linking options:
https://www.mathnet.ru/eng/mendc4507
https://www.mathnet.ru/eng/mendc/v9/i1/p17
This publication is cited in the following 17 articles:
Sofya P. Balabanova, Alexey A. Voronin, Aleksandr M. Churakov, Michael S. Klenov, Vladimir A. Tartakovsky, “Synthetic Strategies for C‐Amino 1,2,3‐Triazoles and Their Oxides: A Review”, Journal of Heterocyclic Chem, 61:12 (2024), 2106
Dmitry M. Bystrov, Leonid L. Fershtat, Nina N. Makhova, “Synthesis and reactivity of aminofuroxans”, Chem Heterocycl Comp, 55:12 (2019), 1143
V. P. Zelenov, A. A. Voronin, A. M. Churakov, Yu. A. Strelenko, M. I. Struchkova, V. A. Tartakovsky, “Amino(tert-butyl-NNO-azoxy)furoxans: synthesis, isomerization, and rearrangement of N-acetyl derivatives”, Russ Chem Bull, 62:1 (2013), 117
S. I. Molotov, A. S. Kulikov, K. A. Lyssenko, N. N. Makhova, “Base-induced rearrangement of 4-amidino-3-R-furoxans into 1-substituted 3-(1-nitroalkyl)-5-R-1H-1,2,4-triazoles”, Russ Chem Bull, 62:5 (2013), 1238
N. N. Makhova, A. S. Kulikov, “Advances in the chemistry of monocyclic amino- and nitrofuroxans”, Russian Chem. Reviews, 82:11 (2013), 1007–1033
Nazariy T. Pokhodylo, Vasyl S. Matiychuk, “Reaction of 1-Aryl-1H-1,2,3-Triazole-4-Carbonyl Chlorides/Isothiocyanates with 3-Amino-5-Methylisoxazole”, Phosphorus, Sulfur, and Silicon and the Related Elements, 186:9 (2011), 1895
L. Larina, V. Lopyrev, Nitroazoles: Synthesis, Structure and Applications, 2009, 81
L. Larina, V. Lopyrev, Nitroazoles: Synthesis, Structure and Applications, 2009, 157
L. Larina, V. Lopyrev, Nitroazoles: Synthesis, Structure and Applications, 2009, 1
G. Nikonov, S. Bobrov, Comprehensive Heterocyclic Chemistry III, 2008, 315
S. I. Molotov, M. A. Epishina, A. S. Kulikov, Yu. V. Nelyubina, K. A. Lyssenko, K. Yu. Suponitsky, N. N. Makhova, “Thermally induced rearrangement of the arylhydrazones of furoxan-3-yl carbonyl compounds”, Mendeleev Commun., 16:5 (2006), 259–262
S. I. Molotov, A. S. Kulikov, N. N. Makhova, K. A. Lyssenko, “Thermal rearrangements of 3-substituted 4-(3-ethoxycarbonylthioureido)-1,2,5-oxadiazole 2-oxides”, Mendeleev Commun., 13:4 (2003), 188–190
I. V. Ovchinnikov, M. A. Epishina, S. I. Molotov, Yu. A. Strelenko, K. A. Lyssenko, N. N. Makhova, “New rearrangement of azofuroxans in an oxidising medium”, Mendeleev Commun., 13:6 (2003), 272–275
Aleksei B. Sheremetev, Nina N. Makhova, Willy Friedrichsen, Advances in Heterocyclic Chemistry, 78, 2001, 65
E. L. Baryshnikova, A. S. Kulikov, I. V. Ovchinnikov, V. V. Solomentsev, N. N. Makhova, “The base-induced cascade rearrangement of 4-acetylamino-3-arylazo-1,2,5-oxadiazole 2-oxides (furoxans) into 4-acetylamino-2-aryl-5-nitro-2H-1,2,3-triazoles”, Mendeleev Commun., 11:6 (2001), 230–232
E. L. Baryshnikova, N. N. Makhova, “Thermal and base-induced rearrangements of furoxanylketones phenylhydrazones”, Mendeleev Commun., 10:5 (2000), 190–192
Nina N. Makhova, Alexander N. Blinnikov, “ChemInform Abstract: New Version of Mononuclear Heterocyclic Rearrangement.”, ChemInform, 30:28 (1999)
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