Asymmetric aldol reactions in ketone/ketone systems catalyzed by ionic liquid-supported C2-symmetrical organocatalyst Научная публикация
| Журнал |
Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436 |
||
|---|---|---|---|
| Вых. Данные | Год: 2015, Том: 25, Номер: 3, Страницы: 168-170 Страниц : 3 DOI: 10.1016/j.mencom.2015.05.002 | ||
| Авторы |
|
||
| Организации |
|
Реферат:
Ionic liquid-supported (1S,2S)- and (1R,2R)-1,2-bis[(S)-prolinamido]-1,2-diphenylethanes act as organocatalysts in asymmetric aldol reactions of acetone with α-keto esters or trifluoroacetophenone providing high yields and from moderate to high enantioselectivity. Recycling of the catalyst with a gradual decrease in conversion and ee values is possible.
Библиографическая ссылка:
Kochetkov S.V.
, Kucherenko A.S.
, Zlotin S.G.
Asymmetric aldol reactions in ketone/ketone systems catalyzed by ionic liquid-supported C2-symmetrical organocatalyst
Mendeleev Communications. 2015. V.25. N3. P.168-170. DOI: 10.1016/j.mencom.2015.05.002 WOS Scopus OpenAlex
Asymmetric aldol reactions in ketone/ketone systems catalyzed by ionic liquid-supported C2-symmetrical organocatalyst
Mendeleev Communications. 2015. V.25. N3. P.168-170. DOI: 10.1016/j.mencom.2015.05.002 WOS Scopus OpenAlex
Идентификаторы БД:
| Web of science: | WOS:000357142000002 |
| Scopus: | 2-s2.0-84930948086 |
| OpenAlex: | W973471862 |