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
In this contribution, we report the first successful baker's yeast reduction of arylpropanones using...
Background: Chiral alcohols are widely used in the synthesis of chiral pharmaceuticals, flavors and...
Gluconobacter oxydans (ATCC 621) were permeabilized with toluene and then lyophilized. This crude en...
Gröger H, Hummel W, Metzner R. Asymmetric Biocatalytic Reduction of Ketones. In: Carreira EM, Yamamo...
Buchholz S, Gröger H. Enationselective Biocatalytic Reduction of Ketones for the Synthesis of Optica...
Kluyveromyces marxianus CBS 6556 growing cell versatility in the enantioselective reduction of keton...
Whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to optically acti...
Catalytic asymmetric reduction of prochiral ketones with the formation of enantio-pure secondary alc...
A novel and efficient reduction of various prochiral ketones such as acetopehones, α-azido aryl keto...
Methods have been studied for the production of chiral alcohols, which are of importance in organic ...
The biocatalytic asymmetric reduction of prochiral ketones for the production of enantiopure alcohol...
The asymmetric reduction of prochiral ketones using isolated or cell-bound ketoreductases is a well-...
Enzymes are able to perform reactions under mild conditions, e.g., pH and temperature, with remarkab...
Alcohol dehydrogenases or carbonyl reductases have been extensively developed for the asymmetric red...
Effective procedures for the synthesis of optically pure alcohols are highly valuable. A commonly em...
In this contribution, we report the first successful baker's yeast reduction of arylpropanones using...
Background: Chiral alcohols are widely used in the synthesis of chiral pharmaceuticals, flavors and...
Gluconobacter oxydans (ATCC 621) were permeabilized with toluene and then lyophilized. This crude en...
Gröger H, Hummel W, Metzner R. Asymmetric Biocatalytic Reduction of Ketones. In: Carreira EM, Yamamo...
Buchholz S, Gröger H. Enationselective Biocatalytic Reduction of Ketones for the Synthesis of Optica...
Kluyveromyces marxianus CBS 6556 growing cell versatility in the enantioselective reduction of keton...
Whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to optically acti...
Catalytic asymmetric reduction of prochiral ketones with the formation of enantio-pure secondary alc...
A novel and efficient reduction of various prochiral ketones such as acetopehones, α-azido aryl keto...
Methods have been studied for the production of chiral alcohols, which are of importance in organic ...
The biocatalytic asymmetric reduction of prochiral ketones for the production of enantiopure alcohol...
The asymmetric reduction of prochiral ketones using isolated or cell-bound ketoreductases is a well-...
Enzymes are able to perform reactions under mild conditions, e.g., pH and temperature, with remarkab...
Alcohol dehydrogenases or carbonyl reductases have been extensively developed for the asymmetric red...
Effective procedures for the synthesis of optically pure alcohols are highly valuable. A commonly em...
In this contribution, we report the first successful baker's yeast reduction of arylpropanones using...
Background: Chiral alcohols are widely used in the synthesis of chiral pharmaceuticals, flavors and...
Gluconobacter oxydans (ATCC 621) were permeabilized with toluene and then lyophilized. This crude en...