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SYNTHESIS OF BICYCLIC BETA-OXO NITRONES - DERIVATIVES OF 6-AZABICYCLO[3.2.1]OCTANE AND THEIR REACTIONS WITH NUCLEOPHILIC-REAGENTS Научная публикация

Журнал Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
ISSN: 0568-5230
Вых. Данные Год: 1991, Том: 40, Номер: 3, Страницы: 597-601 Страниц : 5 DOI: 10.1007/BF00958003
Авторы Reznikov V.A. 1 , Urzhuntseva I.A. 1 , Volodarskii L.B. 1
Организации
1 Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, USSR

Реферат: It was shown that the recyclization of enamino ketones (hydrogenated derivatives of benzimidazole), which proceeds in an acid medium, leads to 6-azabicyclo[3.2.1]-oct-6-en-8-ones. The reactions of these with nucleophilic reagents proceed primarily at the carbonyl group, while reactions with an excess of organometallic reagents with subsequent oxidation lead to stable nitroxide radicals (derivatives of 6-azabicyclo[3.2.l]octane).
Библиографическая ссылка: Reznikov V.A. , Urzhuntseva I.A. , Volodarskii L.B.
SYNTHESIS OF BICYCLIC BETA-OXO NITRONES - DERIVATIVES OF 6-AZABICYCLO[3.2.1]OCTANE AND THEIR REACTIONS WITH NUCLEOPHILIC-REAGENTS
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 1991. V.40. N3. P.597-601. DOI: 10.1007/BF00958003 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 мар. 1991 г.
Идентификаторы БД:
≡ Web of science: WOS:A1991GM58500009
≡ Scopus: 2-s2.0-4544238536
≡ РИНЦ: 30942089
≡ OpenAlex: W1967789347
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