aUral Scientific Research Institute of Technology of Medical Preparations, Ekaterinburg, Russian Federation bChemBridge, Moscow, Russian Federation cDepartment of Chemistry, University of Bremen, Bremen, Germany
Аннотация:
The heating of 5-azauracil 1 with malonamide in butanol resulted in 1,2,3,4,5,6-hexahydro-6-(dicarbamoylmethyl)-1,3,5-triazine- 2,4-dione 3. Under conditions of acid catalysis, compound 1 reacted with o-phenylenediamine, pyrrogallol, resorcinol and phenylhydrazine derivatives to form the corresponding 6-derivatives of 1,2,3,4,5,6-hexahydro-1,3,5-triazine-2,4-dione.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
Yu. A. Azev, S. V. Shorshnev, D. Gabel, “Stable σ-adducts of 5-azauracil with C-nucleophiles”, Mendeleev Commun., 11:6 (2001), 234–235
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4311
https://www.mathnet.ru/rus/mendc/v11/i6/p234
Эта публикация цитируется в следующих 4 статьяx:
H. H. Corzo, O. Dolgounitcheva, V. G. Zakrzewski, J. V. Ortiz, “Valence-Bound and Diffuse-Bound Anions of 5-Azauracil”, J. Phys. Chem. A, 118:34 (2014), 6908
T. A. Tseitler, G. V. Zyryanov, D. S. Kopchuk, I. S. Kovalev, V. L. Rusinov, O. N. Chupakhin, “Synthesis of 8,10-dimethyl-1,10b-dihydro[1,3,5]triazino-[2,1-a]isoindole-2,4,6(3H)-trione by Direct arylation of 1,3,5-triazine-2,4(1H,3H)-dione”, Russ J Org Chem, 50:6 (2014), 783
Ilya N. Egorov, Vladimir L. Rusinov, Oleg N. Chupakhin, “The direct arylation of 1,3,5-triazin-2,4(1H,3H)-dione”, Tetrahedron Letters, 51:13 (2010), 1717
Yurii A. Azev, Sergei V. Shorshnev, Detlef Gabel, “ChemInform Abstract: Stable σ‐Adducts of 5‐Azauracil with C‐Nucleophiles.”, ChemInform, 33:23 (2002)
Обратная связь: