Abstract
N-Nitroso push-pull dyes are unique NO donors, whose NO release is triggered by light and accompanied by a concomitant fluorescence turn-on. Their synthesis involves nitrosation of the corresponding secondary amines, which, however, are not readily available. In this manuscript, we developed a mild, convenient and high-yielding preparation of N-nitroso aryl amines via dealkylative N-nitrosation of tertiary amines. This method is readily employed for the preparation of N-nitrosated rhodamine and coumarin dyes, whose potential as novel NO donors were showcased in cultured cell lines.
| Original language | English |
|---|---|
| Pages (from-to) | 3206-3209 |
| Number of pages | 4 |
| Journal | Organic Chemistry Frontiers |
| Volume | 5 |
| Issue number | 22 |
| DOIs | |
| State | Published - 21 Nov 2018 |
| Externally published | Yes |