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.

Download
Es wurde kein Volltext hochgeladen. Nur Publikationsnachweis!
Zeitschriftenaufsatz | Veröffentlicht | Englisch
Autor
; ; ; ; ; ; ;
Erscheinungsjahr
Zeitschriftentitel
Angewandte Chemie International Edition
Band
45
Zeitschriftennummer
34
Seite
5677-5681
ISSN
eISSN
PUB-ID

Zitieren

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. doi:10.1002/anie.200503394
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.

4 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

On the (Un)greenness of Biocatalysis: Some Challenging Figures and Some Promising Options.
Domínguez de María P, Hollmann F., Front Microbiol 6(), 2015
PMID: 26617592
Investigations on the activity of poly(2-oxazoline) enzyme conjugates dissolved in organic solvents.
Konieczny S, Krumm C, Doert D, Neufeld K, Tiller JC., J Biotechnol 181(), 2014
PMID: 24709400
Miniemulsion as efficient system for enzymatic synthesis of acid alkyl esters.
de Barros DP, Fonseca LP, Cabral JM, Aschenbrenner EM, Weiss CK, Landfester K., Biotechnol Bioeng 106(4), 2010
PMID: 20503297

22 References

Daten bereitgestellt von Europe PubMed Central.


AUTHOR UNKNOWN, 2002

Cheetham, J. Biotechnol. 66(), 1998
Novel bioreduction system for the production of chiral alcohols.
Kataoka M, Kita K, Wada M, Yasohara Y, Hasegawa J, Shimizu S., Appl. Microbiol. Biotechnol. 62(5-6), 2003
PMID: 12838375

Shaw, 2004

Poechlauer, 2004
Bioorganic reactions in microemulsions: the case of lipases.
Stamatis H, Xenakis A, Kolisis FN., Biotechnol. Adv. 17(4-5), 1999
PMID: 14538132

Holmberg, Adv. Colloid Interface Sci. 51(), 1994

Landfester, 2004

AUTHOR UNKNOWN, 0

Taden, Macromol. Rapid Commun. 24(), 2003

AUTHOR UNKNOWN, 0

Cohen, J. Am. Chem. Soc. 86(), 1964

Prashad, Tetrahedron: Asymmetry 9(), 1998

Katayama, Tetrahedron: Asymmetry 9(), 1998

Faulconbridge, Tetrahedron Lett. 41(), 2000

Faber, 2000

Liese, 2000

Yazbeck, Tetrahedron: Asymmetry 15(), 2004
Novel bioreduction system for the production of chiral alcohols.
Kataoka M, Kita K, Wada M, Yasohara Y, Hasegawa J, Shimizu S., Appl. Microbiol. Biotechnol. 62(5-6), 2003
PMID: 12838375

Schmidt, Top. Curr. Chem. 200(), 1999
Kinetic resolution of amino acid esters catalyzed by lipases.
Houng JY, Wu ML, Chen ST., Chirality 8(6), 1996
PMID: 8904833

Export

Markieren/ Markierung löschen
Markierte Publikationen

Open Data PUB

Web of Science

Dieser Datensatz im Web of Science®

Quellen

PMID: 16470761
PubMed | Europe PMC

Suchen in

Google Scholar