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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| Autors principals: | , , , , , , , , , |
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| Format: | Статья |
| Idioma: | English |
| Publicat: |
HeteroCorporation
2018
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| Matèries: | |
| Accés en línia: | 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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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