Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols

Gröger H, Chamouleau F, Orologas N, Rollmann C, Drauz K, Hummel W, Weckbecker A, May O (2006)
Angewandte Chemie International Edition 45(34): 5677-5681.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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DOI
Autor*in
Gröger, HaraldUniBi; Chamouleau, Francoise; Orologas, Nicolas; Rollmann, Claudia; Drauz, Karlheinz; Hummel, Werner; Weckbecker, Andrea; May, Oliver
Einrichtung
Fakultät für Chemie > Industrielle Organische Chemie und Biotechnologie
Erscheinungsjahr
2006
Zeitschriftentitel
Angewandte Chemie International Edition
Band
45
Ausgabe
34
Seite(n)
5677-5681
ISSN
1433-7851
eISSN
1521-3773
Page URI
https://pub.uni-bielefeld.de/record/2347147

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Gröger H, Chamouleau F, Orologas N, et al. Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols. Angewandte Chemie International Edition. 2006;45(34):5677-5681.
Gröger, H., Chamouleau, F., Orologas, N., Rollmann, C., Drauz, K., Hummel, W., Weckbecker, A., et al. (2006). Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols. Angewandte Chemie International Edition, 45(34), 5677-5681. https://doi.org/10.1002/anie.200503394
Gröger, Harald, Chamouleau, Francoise, Orologas, Nicolas, Rollmann, Claudia, Drauz, Karlheinz, Hummel, Werner, Weckbecker, Andrea, and May, Oliver. 2006. “Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols”. Angewandte Chemie International Edition 45 (34): 5677-5681.
Gröger, H., Chamouleau, F., Orologas, N., Rollmann, C., Drauz, K., Hummel, W., Weckbecker, A., and May, O. (2006). Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols. Angewandte Chemie International Edition 45, 5677-5681.
Gröger, H., et al., 2006. Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols. Angewandte Chemie International Edition, 45(34), p 5677-5681.
H. Gröger, et al., “Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols”, Angewandte Chemie International Edition, vol. 45, 2006, pp. 5677-5681.
Gröger, H., Chamouleau, F., Orologas, N., Rollmann, C., Drauz, K., Hummel, W., Weckbecker, A., May, O.: Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols. Angewandte Chemie International Edition. 45, 5677-5681 (2006).
Gröger, Harald, Chamouleau, Francoise, Orologas, Nicolas, Rollmann, Claudia, Drauz, Karlheinz, Hummel, Werner, Weckbecker, Andrea, and May, Oliver. “Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols”. Angewandte Chemie International Edition 45.34 (2006): 5677-5681.

5 Zitationen in Europe PMC

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Domínguez de María P, Hollmann F., Front Microbiol 6(), 2015
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de Barros DP, Fonseca LP, Cabral JM, Aschenbrenner EM, Weiss CK, Landfester K., Biotechnol Bioeng 106(4), 2010
PMID: 20503297

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