Аннотация:
The convenient one-pot synthesis of 5-nitropyridines based on the tricomponent cyclocondensation of nitroacetone, triethyl orthoformate and various enamines has been developed.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
G. P. Sagitullina, A. K. Garkushenko, E. G. Atavin, R. S. Sagitullin, “One-pot synthesis of 5-nitropyridines by the cyclocondensation of nitroacetone, triethyl orthoformate and enamines”, Mendeleev Commun., 19:3 (2009), 155–156
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3152
https://www.mathnet.ru/rus/mendc/v19/i3/p155
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Jun Kuwabara, Yoshiharu Sawada, Mitsuhiro Yoshimatsu, “Copper-Mediated Reactions of Nitriles with Nitromethanes: Aza-Henry Reactions and Nitrile Hydrations”, Org. Lett., 20:4 (2018), 1130
Yulia A. Zobenko, Stefania A. Pozhidaeva, Anna K. Kuratova, Larisa V. Glyzdinskaya, Marina A. Vorontsova, Galina P. Sagitullina, “New method for the synthesis of nitrobiaryls”, Chem Heterocycl Comp, 53:9 (2017), 1014
G. P. Sagitullina, A. K. Garkushenko, M. A. Dushek, N. V. Poendaev, R. S. Sagitullin*, “Synthesis of pyridines by cyclocondensation of acetyl and benzoyl pyruvates with enamines”, Chem Heterocycl Comp, 46:10 (2011), 1250
G. P. Sagitullina, A. K. Garkushenko, L. V. Glyzdinskaya, F. A. Uldashev, M. A. Vorontsova, R. S. Sagitullin**, “NitropyridineS. 9*. Synthesis of substituted 3-amino-5-nitropyridines”, Chem Heterocycl Comp, 46:10 (2011), 1255
A. K. Garkushenko, N. V. Poendaev, M. A. Vorontsova, G. P. Sagitullina, “Nitropyridines 11. *Recyclization of quaternary nitropyridinium salts into substituted nitroanilines”, Chem Heterocycl Comp, 47:4 (2011), 470
G. P. Sagitullina, A. K. Garkushenko, L. V. Glizdinskaya, N. V. Poendaev, D. E. Eremeeva, R. S. Sagitullin, “Nitropyridines. 8.* synthesis of substituted 5-nitronicotinamides”, Chem Heterocycl Comp, 46:5 (2010), 553
Galina P. Sagitullina, Anna K. Garkushenko, Evgeny G. Atavin, Reva S. Sagitullin, “ChemInform Abstract: One‐Pot Synthesis of 5‐Nitropyridines by the Cyclocondensation of Nitroacetone, Triethyl Orthoformate and Enamines.”, ChemInform, 40:42 (2009)
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