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Formation of substituted 6-hydroxy-5-oxo-5,6-dihydrobenzo[c][2,7]naphthyridine upon photochemical transformation of nifedipine Научная публикация

Журнал Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171
Вых. Данные Год: 2003, Том: 52, Номер: 11, Страницы: 2440-2443 Страниц : 4 DOI: 10.1023/B:RUCB.0000012367.57360.18
Ключевые слова 4-(2-nitrophenyl)-3,5-dimethoxycarbonyl-2,6-dimethyl-1,4-dihydropyridine; 4-(2-nitrosophenyl)-3,5-dimethoxycarbonyl-2,6-dimethylpyridine; 2,2 '-bis[3,5-bis(methoxycarbonyl)-2,6-dimethylpyridin-4-yl]azoxybenzene; 6-hydroxy-1-methoxycarbonyl-2,4-dimethyl-5-oxo-5,6-dihydrobenzo[c][2,7]naphthyridine; intramolecular cyclization; photochemistry; nifedipine
Авторы Krivopalov VP 1 , Sedova VF 1 , Shkurko OP 1
Организации
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Реферат: Long-term exposure of nifedipine to daylight in ethanol gives 2,2'-bis[3,5-bis(methoxycarbonyl)-2,6-dimethylpyridin-4-yl]azoxybenzene and 6-hydroxy-1-methoxycarbonyl-2,4-dimetliyl-5-oxo-5,6-dihydrobenzo[c][2,7]naphthyridine as the major products.
Библиографическая ссылка: Krivopalov V. , Sedova V. , Shkurko O.
Formation of substituted 6-hydroxy-5-oxo-5,6-dihydrobenzo[c][2,7]naphthyridine upon photochemical transformation of nifedipine
Russian Chemical Bulletin. 2003. V.52. N11. P.2440-2443. DOI: 10.1023/B:RUCB.0000012367.57360.18 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 нояб. 2003 г.
Идентификаторы БД:
Web of science: WOS:000188800800017
Scopus: 2-s2.0-3543052856
РИНЦ: 13426481
OpenAlex: W2953337955
Цитирование в БД:
БД Цитирований
Web of science 6
Scopus 6
РИНЦ 6
OpenAlex 4
Альметрики: