Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
A streamlined synthetic methodology towards novel tetracyclic 1,4-oxazepines from readily available precursors is described. The compounds, designed as more soluble version of the earlier described, poorly soluble dibenzo[bf][1,4]oxazepines, were obtained in high yields and as a single regioisomer as a result of three tandem chemical events-nucleophilic aromatic substitution, Smiles rearrangement and denitrocyclization. (C) 2014 Elsevier Ltd. All rights reserved.
Язык оригинала | Английский |
---|---|
Страницы (с-по) | 1077-1083 |
Число страниц | 7 |
Журнал | Tetrahedron |
Том | 70 |
Номер выпуска | 5 |
DOI | |
Состояние | Опубликовано - 2014 |
ID: 5708291