Abstract
The reduction of amides to amines has always been a challenging yet attractive process. Herein, we show that in the presence of NaHBEt3 acting as a catalyst, primary, secondary and tertiary amides can be reduced by HBpin, with a wide range of substrates and functional group tolerance. A plausible experimental mechanism is proposed based on control experimental reactions.
| Original language | English |
|---|---|
| Pages (from-to) | 3202-3206 |
| Number of pages | 5 |
| Journal | New Journal of Chemistry |
| Volume | 47 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - 13 Jan 2023 |
| Externally published | Yes |
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