2-Methyl-11-nitro-5,6-dihydro-2H-2,6-methano-1,3,5-benzoxadiazocin-4(3H)-one: synthesis, crystal structure and tautomerism in dipolar aprotic solvents Научная публикация
Журнал |
Mendeleev Communications
ISSN: 0959-9436 |
||
---|---|---|---|
Вых. Данные | Год: 2013, Том: 23, Номер: 3, Страницы: 176-178 Страниц : DOI: 10.1016/j.mencom.2013.05.020 | ||
Авторы |
|
||
Организации |
|
Реферат:
Condensation of salicylaldehyde with nitroacetone and urea yields one diastereomer of the title compound. In DMF or DMSO solutions, this compound undergoes oxadiazocine ring opening leading to the equilibrium between its 2R*, 6S*, 11S*- and 2R*, 6S*,11R*-diastereomers and 4-(2-hydroxyphenyl)-6-methyl-5-nitro-3,4-dihydropyrimidin-2(1H)-one.
Библиографическая ссылка:
Sedova V.F.
, Krivopalov V.P.
, Gatilov Y.V.
, Shkurko O.P.
2-Methyl-11-nitro-5,6-dihydro-2H-2,6-methano-1,3,5-benzoxadiazocin-4(3H)-one: synthesis, crystal structure and tautomerism in dipolar aprotic solvents
Mendeleev Communications. 2013. V.23. N3. P.176-178. DOI: 10.1016/j.mencom.2013.05.020 WOS Scopus РИНЦ
2-Methyl-11-nitro-5,6-dihydro-2H-2,6-methano-1,3,5-benzoxadiazocin-4(3H)-one: synthesis, crystal structure and tautomerism in dipolar aprotic solvents
Mendeleev Communications. 2013. V.23. N3. P.176-178. DOI: 10.1016/j.mencom.2013.05.020 WOS Scopus РИНЦ
Даты:
Опубликована в печати: | 1 мая 2013 г. |
Идентификаторы:
Web of science | WOS:000321540500020 |
Scopus | 2-s2.0-84879096098 |
РИНЦ | 20436238 |
OpenAlex | W2952676182 |