Selective Acylation of 5-Nitro- and 5-Ethoxycarbonyl-4,6-diaryl-3,4-dihydropyrimidin-2(1H)-ones Научная публикация
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Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393 |
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| Вых. Данные | Год: 2010, Том: 46, Номер: 11, Страницы: 1695-1701 Страниц : 7 DOI: 10.1134/S1070428010110163 | ||
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Реферат:
The acetylation and chloroacetylation of 5-nitro- and 5-ethoxycarbonyl-substituted 4,6-diaryl-3,4-dihydropyrimidin-2(1H)-ones proceeds regioselectively at the N-3 atom of the heterocycle whereas the acetylation of the 5-aryloxy-substituted analog results in a mixture of N-1- and N-3-acetylated regioisomers.
Библиографическая ссылка:
Sedova V.F.
, Shkurko O.P.
Selective Acylation of 5-Nitro- and 5-Ethoxycarbonyl-4,6-diaryl-3,4-dihydropyrimidin-2(1H)-ones
Russian Journal of Organic Chemistry. 2010. V.46. N11. P.1695-1701. DOI: 10.1134/S1070428010110163 WOS Scopus РИНЦ
Selective Acylation of 5-Nitro- and 5-Ethoxycarbonyl-4,6-diaryl-3,4-dihydropyrimidin-2(1H)-ones
Russian Journal of Organic Chemistry. 2010. V.46. N11. P.1695-1701. DOI: 10.1134/S1070428010110163 WOS Scopus РИНЦ
Даты:
| Опубликована в печати: | 1 нояб. 2010 г. |
| Опубликована online: | 23 дек. 2010 г. |
Идентификаторы:
| Web of science | WOS:000287033100016 |
| Scopus | 2-s2.0-78651327292 |
| РИНЦ | 16698461 |
| OpenAlex | W2012836304 |