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Ureas as new nucleophilic reagents for SN H amination and carbamoyl amination reactions in the 1,3,7-triazapyrene series

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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Bibliographic Details
Main Authors: Borovlev, I. V., Боровлев, И. В., Demidov, O. P., Демидов, О. П., Amangasieva, G. A., Амангазиева, Г. А., Avakyan, E. K., Авакян, Е. К., Kurnosova, N. A., Курносова, Н. А.
Format: Статья
Language:English
Published: Arkat 2018
Subjects:
1,3,7-triazapyren-6-amines
Amination
Carbamoyl amination
Nucleophilic aromatic substitution of hydrogen
Online Access: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

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