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Ureas as a new nucleophilic reagents for SNAr amination and carbamoyl amination reactions in 1,3,7-triazapyrene series

The ability of urea anions to react as nucleophiles with alkoxy derivatives of 1,3,7-triazapyrenes has been investigated. It was found that against all expectations, the products of the substitution of an alkoxy groups (SN ipso) by amino group were isolated in good yields. The reactions proceed in a...

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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: HeteroCorporation 2018
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Online Access:https://www.scopus.com/record/display.uri?eid=2-s2.0-85010280531&origin=resultslist&sort=plf-f&src=s&st1=Ureas+as+a+New+Nucleophilic+Reagents+for+SNAr+Amination+and+Carbamoyl+Amination+Reactions+in+1%2c3%2c7-Triazapyrene+Series&st2=&sid=60eedcc0553c9716e061af579858b0e1&sot=b&sdt=b&sl=133&s=TITLE-ABS-KEY%28Ureas+as+a+New+Nucleophilic+Reagents+for+SNAr+Amination+and+Carbamoyl+Amination+Reactions+in+1%2c3%2c7-Triazapyrene+Series%29&relpos=0&citeCnt=2&searchTerm=
https://dspace.ncfu.ru/handle/20.500.12258/3076
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