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...
Bewaard in:
| Hoofdauteurs: | , , , , , , , , , |
|---|---|
| Formaat: | Статья |
| Taal: | English |
| Gepubliceerd in: |
HeteroCorporation
2018
|
| Onderwerpen: | |
| Online toegang: | 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 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|
Internet
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