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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| Huvudupphovsmän: | , |
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| Materialtyp: | Статья |
| Språk: | English |
| Publicerad: |
Elsevier Ltd
2018
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| Länkar: | 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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