Ureas as new nucleophilic reagents for SN H amination and carbamoyl amination reactions in the 1,3,7-triazapyrene series
The ability of urea anions to react as nucleophiles with 1,3,7-triazapyrenes has been investigated. It was found that, against all expectations, the products of the substitution of hydrogen (SN H) by an amino group were isolated in good yields. The reactions proceed in anhydrous DMSO solution at roo...
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| Автори: | , , , , , , , , , |
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| Формат: | Статья |
| Мова: | English |
| Опубліковано: |
Arkat
2018
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| Предмети: | |
| Онлайн доступ: | https://www.scopus.com/record/display.uri?eid=2-s2.0-84960124757&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=b34ee1a283c2e8415711b601b248f06f&sot=afnl&sdt=cl&cluster=scopubyr%2c%222016%22%2ct&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&relpos=81&citeCnt=6&searchTerm= https://dspace.ncfu.ru/handle/20.500.12258/3298 |
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https://www.scopus.com/record/display.uri?eid=2-s2.0-84960124757&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=b34ee1a283c2e8415711b601b248f06f&sot=afnl&sdt=cl&cluster=scopubyr%2c%222016%22%2ct&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&relpos=81&citeCnt=6&searchTerm=https://dspace.ncfu.ru/handle/20.500.12258/3298