Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
The direction of the cyclocondensation of 2-fluoro-5-nitrobenzaldehyde with five amidines having α-hydrogen atoms has been studied. It was established that depending on the structure of the amidine the main products of the reaction may be not only quinazolines but also 3-aminoisoquinolines. A new convenient route has been found for the synthesis of 3-aminoisoquinolines consisting of the cyclocondensation of α-acylacetamidines with 2-fluoro-5-nitrobenzaldehyde.
Язык оригинала | английский |
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Страницы (с-по) | 888-894 |
Число страниц | 7 |
Журнал | Chemistry of Heterocyclic Compounds |
Том | 40 |
Номер выпуска | 7 |
DOI | |
Состояние | Опубликовано - 1 июл 2004 |
ID: 36262537