A C3-symmetrical chiral trisoxazoline zinc complex as a functional model for zinc hydrolases: kinetic resolution of racemic chiral esters by transesterification
Mimicking the activity of tris(histidine)zinc-based enzymes, chiral dinuclear trisoxazolinezinc complexes such as the triflato cation (see picture) are the first non-enzymatic catalysts for the asymmetric transesterification of activated esters. First results of the kinetic resolution of amino acid...
Gespeichert in:
| Hauptverfasser: | , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
25 August 2004
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| In: |
Angewandte Chemie. International edition
Year: 2004, Jahrgang: 43, Heft: 34, Pages: 4479-4482 |
| ISSN: | 1521-3773 |
| DOI: | 10.1002/anie.200460187 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/anie.200460187 Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.200460187 
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| Verfasserangaben: | Clémence Dro, Stéphane Bellemin-Laponnaz, Richard Welter, and Lutz H. Gade |
MARC
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| 520 | |a Mimicking the activity of tris(histidine)zinc-based enzymes, chiral dinuclear trisoxazolinezinc complexes such as the triflato cation (see picture) are the first non-enzymatic catalysts for the asymmetric transesterification of activated esters. First results of the kinetic resolution of amino acid phenolates establish the stereoselectivity for this reaction. (F pink, N blue, O red, S yellow, Zn cyan) | ||
| 650 | 4 | |a asymmetric catalysis | |
| 650 | 4 | |a biomimetic synthesis | |
| 650 | 4 | |a chirality | |
| 650 | 4 | |a tripodal ligands | |
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