Alkylation of Enaminoketone with a Modified Carane Skeleton. Formation of Stable β-Diketone Monoimines Научная публикация
| Журнал |
Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393 |
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| Вых. Данные | Год: 1997, Том: 33, Номер: 5, Страницы: 601-606 Страниц : 6 | ||
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| Организации |
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Реферат:
Alkylation of a bicyclic enaminoketone, 1-[(1R,5R)-3-amino-6,6-dimethylbicyclo[3.1.0]hex-2-en-2-yl)]ethanone, with highly reactive alkyl halides (methyl iodide, benzyl halides, and allyl halides) in a two-phase system benzene-40% aqueous NaOH in the presence of benzyltriethylammonium chloride (BTEA) as phase-transfer catalyst results in formation of stable β-diketone monoimines, derivatives of the series of 1-[(1R,5R)-2-alkyl-3-imino-6,6-dimethylbicyclo[3.1.0]hex-2-yl]ethanone, in 53-81% yields.
Библиографическая ссылка:
Tkachev A.V.
, Popov S.A.
Alkylation of Enaminoketone with a Modified Carane Skeleton. Formation of Stable β-Diketone Monoimines
Russian Journal of Organic Chemistry. 1997. V.33. N5. P.601-606. Scopus РИНЦ
Alkylation of Enaminoketone with a Modified Carane Skeleton. Formation of Stable β-Diketone Monoimines
Russian Journal of Organic Chemistry. 1997. V.33. N5. P.601-606. Scopus РИНЦ
Оригинальная версия:
Tkachev A.V.
, Popov S.A.
Alkylation of enaminoketone with modified carane skeleton. Formation of beta-diketone stable monoimines
Журнал органической химии (RUSS J ORG CHEM+). 1997. V.33. N5. P.660-665. WOS
Alkylation of enaminoketone with modified carane skeleton. Formation of beta-diketone stable monoimines
Журнал органической химии (RUSS J ORG CHEM+). 1997. V.33. N5. P.660-665. WOS
Идентификаторы:
| Scopus | 2-s2.0-0347107769 |
| РИНЦ | 13261524 |