A C3-symmetrical chiral trisoxazoline zinc complex as a functional model for zinc hydrolases: kinetic resolution of racemic chiral esters by rransesterification
Der Aktivität von Enzymen mit Tris(histidin)zink-Zentren eifern chirale Trisoxazolinzink-Zweikernkomplexe nach. Das abgebildete Triflato-Kation ist einer dieser ersten nichtenzymatischen Katalysatoren für die asymmetrische Umesterung von aktivierten Estern. Erste Ergebnisse für die kinetische Rac...
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| Hauptverfasser: | , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
25 August 2004
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| In: |
Angewandte Chemie
Year: 2004, Jahrgang: 116, Heft: 34, Pages: 4579-4582 |
| ISSN: | 1521-3757 |
| DOI: | 10.1002/ange.200460187 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/ange.200460187 Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ange.200460187 
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| Verfasserangaben: | Clémence Dro, Stéphane Bellemin-Laponnaz, Richard Welter, and Lutz H. Gade |
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| 520 | |a Der Aktivität von Enzymen mit Tris(histidin)zink-Zentren eifern chirale Trisoxazolinzink-Zweikernkomplexe nach. Das abgebildete Triflato-Kation ist einer dieser ersten nichtenzymatischen Katalysatoren für die asymmetrische Umesterung von aktivierten Estern. Erste Ergebnisse für die kinetische Racematspaltung von Aminosäurephenylestern belegen die Stereoselektivität der Reaktion (F rosa, N blau, O rot, S gelb, Zn grün). | ||
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