Abstract
We developed a novel method for direct C3 carbamoylation of 2H-indazoles using oxamic acids as carbamoyl radical sources. In the presence of ammonium persulfate, carbamoyl radicals were generated from oxamic acids, then used for further reactions with 2H-indazoles to afford the desired products. The reaction proceeds under metal- and catalyst-free conditions. This simple process allows for the efficient synthesis of C3 carbamoylated 2H-indazoles, which are important scaffolds in organic synthesis.
| Original language | English |
|---|---|
| Pages (from-to) | 3382-3385 |
| Number of pages | 4 |
| Journal | European Journal of Organic Chemistry |
| Volume | 2021 |
| Issue number | 23 |
| DOIs | |
| State | Published - 2021.06.21 |
Keywords
- 2H-Indazoles
- Carbamoylation
- Minisci reaction
- Radical reaction
- Synthetic methods
Quacquarelli Symonds(QS) Subject Topics
- Engineering - Petroleum
- Chemistry
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