Аннотация:
2,4,6-Triazido-3-chloro-5-cyanopyridine reacts with pyrrolidine and piperidine to form corresponding 2-azido-4,6-diamino-3-chloro-5-cyanopyridines in high yields.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
S. V. Chapyshev, “Nucleophilic replacement of the azido groups by amines in 2,4,6-triazido-3-chloro-5-cyanopyridine”, Mendeleev Commun., 17:5 (2007), 287–288
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3460
https://www.mathnet.ru/rus/mendc/v17/i5/p287
Эта публикация цитируется в следующих 6 статьяx:
Silvia E. Loredo-Carrillo, Elisa Leyva, Matthew S. Platz, Agobardo Cárdenas-Chaparro, Antonio Martínez-Richa, “Thermolysis of 2-azido-3-(R-anilino)-1,4-naphthoquinones. Nitrene insertion versus hydrogen abstraction”, Tetrahedron Letters, 61:14 (2020), 151731
Sergei Chapyshev, “Six-Membered Aromatic Polyazides: Synthesis and Application”, Molecules, 20:10 (2015), 19142
S. V. Chapyshev, D. V. Korchagin, G. V. Shilov, S. M. Aldoshin, “Synthesis and structure of 2,6-diazidotrichloropyridine N-oxide”, Russ J Org Chem, 47:9 (2011), 1323
Yu. M. Mikhailov, S. V. Chapyshev, V. V. Nedel'ko, “Synthesis, thermal stability, heats of formation, and explosive properties of cyano-substituted di-, tri-, and tetraazidopyridines”, Russ Chem Bull, 58:10 (2009), 2097
Sergei V. Chapyshev, “ChemInform Abstract: Nucleophilic Replacement of the Azido Groups by Amines in 2,4,6‐Triazido‐3‐chloro‐5‐cyanopyridine.”, ChemInform, 39:9 (2008)
M. R. Crampton, Organic Reaction Mechanisms Series, Organic Reaction Mechanisms · 2007, 2007, 155
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