A General and Scalable Synthesis of Polysubstituted Indoles
A consecutive 2-step synthesis of <i>N</i>-unprotected polysubstituted indoles bearing an electron-withdrawing group at the C-3 position from readily available nitroarenes is reported. The protocol is based on the [3,3]-sigmatropic rearrangement of <i>N</i>-oxyenamines generated by the DABCO-catalyz...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
MDPI AG
2020-11-01
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| Edice: | Molecules |
| Témata: | |
| On-line přístup: | https://www.mdpi.com/1420-3049/25/23/5595 |
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