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Generation and metathesis of azomethine imines in reaction of 6-aryl-1,5-diazabicyclo[3.1.0]hexanes with het(aryl)methylidenemalononitriles Научная публикация

Журнал Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Вых. Данные Год: 2013, Том: 62, Номер: 4, Страницы: 1066-1075 Страниц : 10 DOI: 10.1007/s11172-013-0143-9
Авторы Pleshchev M.I. 1 , Petukhova V.Yu. 1 , Kuznetsov V.V. 1 , Khakimov D.V. 1 , Pivina T.S. 1 , Nelyubina Yu.V. 2 , Makhova N.N. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
2 A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Moscow, Russian Federation

Реферат: A new metathesis reaction of azomethine imines is found. Catalytic or thermal diaziridine ring opening of 6-aryl-1,5-diazabicyclo[3.1.0]hexanes leads to azomethine imines reacting further with het(aryl)methylidenemalononitriles to give in situ new azomethine imines inaccessible by common synthetic methods. New azomethine imines are detected as pyrazolines formed via a 1,4-H shift and trapped by the [3+2] cycloaddition with various dipolarophiles to yield 1,5-diazabicyclo[3.3.0]octane derivatives bearing pharmacophoric heterocycles, e.g. furan, nitrofuran, thiophene, and indole. The best results are achieved in the Et2O·BF3-catalyzed reactions in ionic liquids.
Библиографическая ссылка: Pleshchev M.I. , Petukhova V.Y. , Kuznetsov V.V. , Khakimov D.V. , Pivina T.S. , Nelyubina Y.V. , Makhova N.N.
Generation and metathesis of azomethine imines in reaction of 6-aryl-1,5-diazabicyclo[3.1.0]hexanes with het(aryl)methylidenemalononitriles
Russian Chemical Bulletin. 2013. V.62. N4. P.1066-1075. DOI: 10.1007/s11172-013-0143-9 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000331392200026
Scopus: 2-s2.0-84897724446
OpenAlex: W2066270311
Цитирование в БД:
БД Цитирований
OpenAlex 13
Scopus 11
Web of science 11
Альметрики: