Аннотация:
Treatment of nitrofurazans (NF) with sulfur nucleophiles affords a wide variety of product types, depending on the structure of both NF and S-nucleophiles.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
A. B. Sheremetev, E. V. Mantseva, N. S. Aleksandrova, V. S. Kuz'min, L. I. Khmel'nitskii, “Reaction of Nitrofurazans with Sulfur Nucleophiles”, Mendeleev Commun., 5:1 (1995), 25–27
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc5019
https://www.mathnet.ru/rus/mendc/v5/i1/p25
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Robert D. Chapman, William S. Wilson, John W. Fronabarger, Lawrence H. Merwin, Gregory S. Ostrom, “Prospects of fused polycyclic nitroazines as thermally insensitive energetic materials”, Thermochimica Acta, 384:1-2 (2002), 229
Aleksei B. Sheremetev, Nina N. Makhova, Willy Friedrichsen, Advances in Heterocyclic Chemistry, 78, 2001, 65
Aleksei B. Sheremetev, Natalya S. Aleksandrova, Tatyana M. Melnikova, Tatyana S. Novikova, Yuri A. Strelenko, Dmitrii E. Dmitriev, “Synthesis of difurazanyl ethers from 4,4?-dinitroazoxyfurazan”, Heteroatom Chem., 11:1 (2000), 48
A. B. Sheremetev, N. S. Aleksandrova, E. V. Mantseva, D. E. Dmitriev, “Synthesis of chlorofurazans from nitrofurazans”, Mendeleev Commun., 10:2 (2000), 67–69
A. B. Sheremetev, N. S. Aleksandrova, “An efficient synthesis of hydroxyfurazans”, Mendeleev Commun., 8:6 (1998), 238–239
R. Michael Paton, Comprehensive Heterocyclic Chemistry II, 1996, 229
Comprehensive Heterocyclic Chemistry II, 1996, 905
G.V. Boyd, Progress in Heterocyclic Chemistry, 8, 1996, 192
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A. B. Sheremetev, I. L. Yudin, “Synthesis of unsubstituted 4H,8H-bisfurazano[3,4-b:3′,4′-e]pyrazine”, Mendeleev Commun., 6:6 (1996), 247–248
A. B. SHEREMETEV, E. V. MANTSEVA, N. S. ALEKSANDROVA, V. S. KUZ'MIN, L. I. KHMEL'NITSKII, “ChemInform Abstract: Reaction of Nitrofurazans with Sulfur Nucleophiles.”, ChemInform, 26:26 (1995)
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