Copper-boxmi complexes as highly enantioselective catalysts for electrophilic trifluoromethylthiolations
The enantioselective trifluoromethylthiolation of β-ketoesters using chiral copper-boxmi complexes as catalysts is reported. A number of α-SCF3-substituted β-ketoesters have been obtained with up to >99 % enantiomeric excess (ee), and the trifluoromethylthiolated products were then transformed di...
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| Hauptverfasser: | , , , |
|---|---|
| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2014
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| In: |
Chemistry - a European journal
Year: 2013, Jahrgang: 20, Heft: 1, Pages: 93-97 |
| ISSN: | 1521-3765 |
| DOI: | 10.1002/chem.201303641 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/chem.201303641 Verlag, lizenzpflichtig, Volltext: https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.201303641 |
| Verfasserangaben: | Qing-Hai Deng, Christoph Rettenmeier, Hubert Wadepohl, and Lutz H. Gade |
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| 520 | |a The enantioselective trifluoromethylthiolation of β-ketoesters using chiral copper-boxmi complexes as catalysts is reported. A number of α-SCF3-substituted β-ketoesters have been obtained with up to >99 % enantiomeric excess (ee), and the trifluoromethylthiolated products were then transformed diastereoselectively to α-SCF3-β-hydroxyesters with two adjacent quaternary stereocenters. | ||
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