|
Эта публикация цитируется в 7 научных статьях (всего в 7 статьях)
Diastereoselective synthesis of 3-substituted acylamino-3,4-dihydro-1,2,4-triazinones
I. N. Egorova, B. Königb, V. L. Rusinova, O. N. Chupakhinac a Department of Organic Chemistry, Urals State Technical University, Ekaterinburg, Russian Federation
b Institut für Organishce Chemie, Universität Regensburg, Regensburg, Germany
c I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
Аннотация:
6-Phenyl-1,2,4-triazin-5(4H)-one 1 reacts with C-nucleophiles, such as indole, in the presence of N-acetylamino acids, to yield 2-acyl-3-indolyl-6-phenyl-3,4-dihydro-1,2,4-triazin-5(4H)-ones 2–6 with high diastereoselectivity.
Ключевые слова:
1.2.4-triazines, diastereoselective synthesis, amino acids, indoles.
Образец цитирования:
I. N. Egorov, B. König, V. L. Rusinov, O. N. Chupakhin, “Diastereoselective synthesis of 3-substituted acylamino-3,4-dihydro-1,2,4-triazinones”, Mendeleev Commun., 18:2 (2008), 99–101
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3263 https://www.mathnet.ru/rus/mendc/v18/i2/p99
|
Статистика просмотров: |
Страница аннотации: | 30 | PDF полного текста: | 6 |
|