Whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to optically active alcohols. Currently, most of the whole-cell catalytic performance involves resting cells rather than growing cell biotransformation, which is one-step process that benefits from the simultaneous growth and biotransformation, eliminating the need for catalysts preparation. In this paper, asymmetric reduction of 14 aromatic ketones to the corresponding enantiomerically pure alcohols was successfully conducted using the growing and resting cells of marine-derived fungi under optimized conditions. Good yields and excellent enantioselectivities were achieved with both methods. Although substrate inhibition might be a limiting factor for growing...
Alcohol dehydrogenases or carbonyl reductases have been extensively developed for the asymmetric red...
Biocatalytic processes represent one of the most heavily used green methodologies in preparative che...
In this study, a new strategy was developed for efficient synthesis of chiral aryl alcohols mediated...
Whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to optically acti...
The biocatalytic asymmetric reduction of prochiral ketones for the production of enantiopure alcohol...
In this study, four bacterial strains were tested for their ability to reduce acetophenones to its c...
Gröger H, Hummel W, Metzner R. Asymmetric Biocatalytic Reduction of Ketones. In: Carreira EM, Yamamo...
The use of microorganism growing cells is a well recognized methodology in biocatalyzed organic reac...
Kluyveromyces marxianus CBS 6556 growing cell versatility in the enantioselective reduction of keton...
Enzymes are able to perform reactions under mild conditions, e.g., pH and temperature, with remarkab...
The use of microorganism growing cells is a well recognized methodology in biocatalyzed organic reac...
Gluconobacter oxydans (ATCC 621) were permeabilized with toluene and then lyophilized. This crude en...
Chiral secondary alcohols are valuable intermediates for many important enantiopure pharmaceuticals ...
In this contribution, we report the first successful baker's yeast reduction of arylpropanones using...
Immobilized cells of the yeast Cryptococcus laurentii attached to calcium alginate have been introdu...
Alcohol dehydrogenases or carbonyl reductases have been extensively developed for the asymmetric red...
Biocatalytic processes represent one of the most heavily used green methodologies in preparative che...
In this study, a new strategy was developed for efficient synthesis of chiral aryl alcohols mediated...
Whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to optically acti...
The biocatalytic asymmetric reduction of prochiral ketones for the production of enantiopure alcohol...
In this study, four bacterial strains were tested for their ability to reduce acetophenones to its c...
Gröger H, Hummel W, Metzner R. Asymmetric Biocatalytic Reduction of Ketones. In: Carreira EM, Yamamo...
The use of microorganism growing cells is a well recognized methodology in biocatalyzed organic reac...
Kluyveromyces marxianus CBS 6556 growing cell versatility in the enantioselective reduction of keton...
Enzymes are able to perform reactions under mild conditions, e.g., pH and temperature, with remarkab...
The use of microorganism growing cells is a well recognized methodology in biocatalyzed organic reac...
Gluconobacter oxydans (ATCC 621) were permeabilized with toluene and then lyophilized. This crude en...
Chiral secondary alcohols are valuable intermediates for many important enantiopure pharmaceuticals ...
In this contribution, we report the first successful baker's yeast reduction of arylpropanones using...
Immobilized cells of the yeast Cryptococcus laurentii attached to calcium alginate have been introdu...
Alcohol dehydrogenases or carbonyl reductases have been extensively developed for the asymmetric red...
Biocatalytic processes represent one of the most heavily used green methodologies in preparative che...
In this study, a new strategy was developed for efficient synthesis of chiral aryl alcohols mediated...