Stereoselective synthesis of trifluoromethyl-substituted 2H-furan-amines from enaminones
A straightforward strategy for synthesis of highly functionalized trifluoromethyl 2H-furans is described. The copper catalyzed method relies on a cascade cyclic reaction between enaminones and N-tosylhydrazones. This method allows the synthesis of 2-amino-3-trifluoromethyl-substituted 2H-furan deriv...
| Autori principali: | , , , , , , , |
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| Altri autori: | |
| Natura: | Journal Article |
| Lingua: | English |
| Pubblicazione: |
2022
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| Soggetti: | |
| Accesso online: | https://hdl.handle.net/10356/160880 |