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Reaction of benzyne with 1,2,3,4-tetrahydroisoquinolines as an access to 1H-3-benzazepines

1,2,3,4-Tetrahydroisoquinolines bearing phenacyl group at the nitrogen atom in their reaction with benzyne in acetonitrile undergo ring expansion to give 1H-3-benzazepines

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Главные авторы: Aksenov, A. V., Аксенов, А. В.
格式: Статья
语言:English
出版: Elsevier Ltd 2018
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在线阅读:https://www.scopus.com/record/display.uri?eid=2-s2.0-85041621297&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=nort*+caucas*+fed*+univ*&sid=3d154567276ef664a27b36889397448a&sot=afnl&sdt=sisr&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&ref=%28Reaction+of+benzyne+with+1%2c2%2c3%2c4-tetrahydroisoquinolines+as+an+access+to+1H-3-benzazepines%29&relpos=0&citeCnt=0&searchTerm=
https://dspace.ncfu.ru:443/handle/20.500.12258/325
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