Chiral alcohols are useful intermediates and auxiliaries in organic synthesis. Their preparation in enantiopure form is consequently of very high interest. Among the different enzymatic procedures, the use of dehydrogenase activities can be considered as the most attractive alternative. These enzymes can fruitfully work in inverse direction as enantioselective reducing agents. We will focus on the use of well-known alcohol dehydrogenases, describing their application in chiral alcohol preparation. A final discussion on the possibility of using these enzymes in either oxidative or reductive direction will be presented
Although biotransformations implementing alcohol dehydrogenases (ADHs) are widespread, enzymes which...
Three dehydrogenases – (R)-alcohol dehydrogenase from L. kefir, (S)-aromatic alcohol dehydrogenase f...
Alcohol dehydrogenases are enzymes involved in natural oxidoreductive interconversions between alcoh...
The redox equilibrium between alcohol - carbonyl groups is greatly used by enzymes and chemists to p...
Chiral β-nitroalcohols are important building blocks in organic chemistry. The synthetic approa...
Enantiomerically enriched chiral secondary alcohols serve as valuable building blocks for drug inter...
Alcohol dehydrogenases are of high interest for the stereoselective synthesis of building blocks wit...
Alcohol dehydrogenases have fascinated chemists over the span of a few decades to catalyze oxidation...
The demand for optically pure secondary alcohols, which has grown rapidly in recent years, has spurr...
Enzymes act as biocatalysts whether are also mediating in all anabolic and catabolic pathways, playi...
The importance of chiral alcohols as starting materials for the production of fine chemicals and as ...
Racemic or enantiomerically pure alcohols can be converted with high yield into enantiopure chiral a...
The use of enzymes as catalysts for chemical transformations has emerged as a “greener” alternative ...
Chiral β-nitroalcohols are important building blocks in organic chemistry. The synthetic approach Ch...
Enantioselective reductions are a key to successful target-oriented syntheses. Finding the most suit...
Although biotransformations implementing alcohol dehydrogenases (ADHs) are widespread, enzymes which...
Three dehydrogenases – (R)-alcohol dehydrogenase from L. kefir, (S)-aromatic alcohol dehydrogenase f...
Alcohol dehydrogenases are enzymes involved in natural oxidoreductive interconversions between alcoh...
The redox equilibrium between alcohol - carbonyl groups is greatly used by enzymes and chemists to p...
Chiral β-nitroalcohols are important building blocks in organic chemistry. The synthetic approa...
Enantiomerically enriched chiral secondary alcohols serve as valuable building blocks for drug inter...
Alcohol dehydrogenases are of high interest for the stereoselective synthesis of building blocks wit...
Alcohol dehydrogenases have fascinated chemists over the span of a few decades to catalyze oxidation...
The demand for optically pure secondary alcohols, which has grown rapidly in recent years, has spurr...
Enzymes act as biocatalysts whether are also mediating in all anabolic and catabolic pathways, playi...
The importance of chiral alcohols as starting materials for the production of fine chemicals and as ...
Racemic or enantiomerically pure alcohols can be converted with high yield into enantiopure chiral a...
The use of enzymes as catalysts for chemical transformations has emerged as a “greener” alternative ...
Chiral β-nitroalcohols are important building blocks in organic chemistry. The synthetic approach Ch...
Enantioselective reductions are a key to successful target-oriented syntheses. Finding the most suit...
Although biotransformations implementing alcohol dehydrogenases (ADHs) are widespread, enzymes which...
Three dehydrogenases – (R)-alcohol dehydrogenase from L. kefir, (S)-aromatic alcohol dehydrogenase f...
Alcohol dehydrogenases are enzymes involved in natural oxidoreductive interconversions between alcoh...