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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...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: 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.
التنسيق: Статья
اللغة:English
منشور في: HeteroCorporation 2018
الموضوعات:
الوصول للمادة أونلاين: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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