The one-pot multistep enzymatic oxidation of aliphatic and benzylic alcohols to the corresponding aldehydes combined with their subsequent carboligation to chiral α-hydroxy ketones has been exemplarily evaluated in terms of being a “green” biocatalytic approach. Besides the potential to start from bio-derived alcohols, this concept avoids the direct use of the reactive aldehyde intermediates, enables addition of high substrate concentrations in one liquid phase while maintaining enzyme activity and enables a simplified product isolation with diminished waste formation
Bioreduction has emerged over the years as an alternative method to organic synthesis for the genera...
Alcohol dehydrogenases have fascinated chemists over the span of a few decades to catalyze oxidation...
The development of efficient syntheses for enantiomerically enriched alpha-hydroxy ketones is an imp...
The one-pot multistep enzymatic oxidation of aliphatic and benzylic alcohols to the corresponding al...
The demand for optically pure secondary alcohols, which has grown rapidly in recent years, has spurr...
Racemic or enantiomerically pure alcohols can be converted with high yield into enantiopure chiral a...
Biocatalysis offers tremendous advantages to generate complex chiral compounds in high enantiomeric ...
Quaternary stereocenters are privileged structural motifs, widely distributed in natural products an...
The implementation of light-driven catalytic processes in biocatalysis opens a golden window of oppo...
A three-step biocatalytic procedure is described for the conversion of methyl and ethyl cyclopentene...
The oxidation of alcohols to carbonyl compounds is one of the most important reactions in organic ch...
Gröger H, Hummel W, Metzner R. Asymmetric Biocatalytic Reduction of Ketones. In: Carreira EM, Yamamo...
The implementation of light-driven catalytic processes in biocatalysis opens a golden window of oppo...
Alcohol dehydrogenases are of high interest for the stereoselective synthesis of building blocks wit...
A chemo- and biocatalytic cascade approach was applied for the stereoselective synthesis of hydroxy ...
Bioreduction has emerged over the years as an alternative method to organic synthesis for the genera...
Alcohol dehydrogenases have fascinated chemists over the span of a few decades to catalyze oxidation...
The development of efficient syntheses for enantiomerically enriched alpha-hydroxy ketones is an imp...
The one-pot multistep enzymatic oxidation of aliphatic and benzylic alcohols to the corresponding al...
The demand for optically pure secondary alcohols, which has grown rapidly in recent years, has spurr...
Racemic or enantiomerically pure alcohols can be converted with high yield into enantiopure chiral a...
Biocatalysis offers tremendous advantages to generate complex chiral compounds in high enantiomeric ...
Quaternary stereocenters are privileged structural motifs, widely distributed in natural products an...
The implementation of light-driven catalytic processes in biocatalysis opens a golden window of oppo...
A three-step biocatalytic procedure is described for the conversion of methyl and ethyl cyclopentene...
The oxidation of alcohols to carbonyl compounds is one of the most important reactions in organic ch...
Gröger H, Hummel W, Metzner R. Asymmetric Biocatalytic Reduction of Ketones. In: Carreira EM, Yamamo...
The implementation of light-driven catalytic processes in biocatalysis opens a golden window of oppo...
Alcohol dehydrogenases are of high interest for the stereoselective synthesis of building blocks wit...
A chemo- and biocatalytic cascade approach was applied for the stereoselective synthesis of hydroxy ...
Bioreduction has emerged over the years as an alternative method to organic synthesis for the genera...
Alcohol dehydrogenases have fascinated chemists over the span of a few decades to catalyze oxidation...
The development of efficient syntheses for enantiomerically enriched alpha-hydroxy ketones is an imp...