Enantioselective addition of carbon acids to α-nitroalkenes: the first asymmetric aminocatalytic reaction in liquefied carbon dioxide Научная публикация
| Журнал |
Tetrahedron Letters
ISSN: 0040-4039 , E-ISSN: 1873-3581 |
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| Вых. Данные | Год: 2012, Том: 53, Номер: 27, Страницы: 3502-3505 Страниц : 4 DOI: 10.1016/j.tetlet.2012.04.123 | ||
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Реферат:
Carbon acids, in particular malonates, malononitrile, and anthranone, react enantioselectively with α-nitroalkenes in the presence of Takemoto’s organocatalyst in liquid carbon dioxide medium (100 bar, rt), under homogeneous conditions, to afford the corresponding Michael adducts in moderate to high yields and with enantioselectivities comparable with those obtained in organic solvents.
Библиографическая ссылка:
Nigmatov A.G.
, Kuchurov I.V.
, Siyutkin D.E.
, Zlotin S.G.
Enantioselective addition of carbon acids to α-nitroalkenes: the first asymmetric aminocatalytic reaction in liquefied carbon dioxide
Tetrahedron Letters. 2012. V.53. N27. P.3502-3505. DOI: 10.1016/j.tetlet.2012.04.123 WOS Scopus OpenAlex
Enantioselective addition of carbon acids to α-nitroalkenes: the first asymmetric aminocatalytic reaction in liquefied carbon dioxide
Tetrahedron Letters. 2012. V.53. N27. P.3502-3505. DOI: 10.1016/j.tetlet.2012.04.123 WOS Scopus OpenAlex
Идентификаторы БД:
| Web of science: | WOS:000306152500024 |
| Scopus: | 2-s2.0-84861644323 |
| OpenAlex: | W2098278542 |