Abstract
Herein, the visible-light-induced α-C(sp3)-H amination reactions of tertiary amines were reported. By using readily available 1, 3-dioxoisoindolin-2-yl benzoate as precursor of N-radical and blue LEDs as green and sustainable energy source, the α-C(sp3)-H bonds of various N, N-dimethylaniline derivatives were aminated directly. Based on radical trapping experiment and documented literature, a mechanism involving radicals coupling was proposed. This method featured in mild reaction conditions and good functional group tolerance, which provides a simple and practical protocol to the modification of tertiary amines.
| Translated title of the contribution | Visible-Light-Induced α-C(sp3)-H Amination Reactions of Tertiary Amines |
|---|---|
| Original language | Chinese (Traditional) |
| Pages (from-to) | 133-139 |
| Number of pages | 7 |
| Journal | Chinese Journal of Organic Chemistry |
| Volume | 40 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1 Jan 2020 |
| Externally published | Yes |
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