The biohydrogenation of 2-substituted allyl alcohols 1a-c proceeds enantioselectively (95-98% ee) to afford (R)-2-methyl alkanols 2a-c
The microbial enantioselective reduction of C4-C8 methylketones to the corresponding (R)-alcohols wa...
Although biotransformations implementing alcohol dehydrogenases (ADHs) are widespread, enzymes which...
Stereoselective reduction of prochiral ketones to the corresponding alcohols using biocatalysts has ...
The baker's yeast mediated biohydrogenation of unsaturated compounds containing a methylene group ma...
The baker's yeast biohydrogenation of the 2-substituted allyl alcohol 2a, in turn prepared from dihy...
Ethyl 4,4-dimethoxy-3-methylbut-2-enoate (1; R = CO2Et) has been prepared as a mixture of (E)-and (Z...
The baker’s yeast mediated reduction of 2-acetyl-3-methyl sulfolane 1 to provide the corresponding a...
(E)-2-methyl- and (E)-3-methyl-2,4-pentadien-1-ols are reduced to (S)-2-methyl- and (S)-3-methyl-4-p...
Reduction of a series of para-substituted 2-methyl-cinnamaldehy- des (1-7) at 20 °C and at pH = 2-3 ...
Microbial synthesis is an important contribution to Green Chemistry and production-integrated enviro...
This article summarizes our recent developments in allylic alcohol functionalization by the intercon...
α-Chiral amines are key intermediates for the synthesis of a plethora of chemical compounds at indus...
The stereoselective synthesis of (S)- and (R)-3-allyloxy-propane-1,2-diol has been accomplished in f...
Baker's yeast reduction of 1-(4-methoxyphenyl)propan-2-one, 4-phenylbutan-2-one, and 2-hydroxy-1-(4-...
This book is a collection of studies focused on the exploitation of enzyme stereoselectivity for the...
The microbial enantioselective reduction of C4-C8 methylketones to the corresponding (R)-alcohols wa...
Although biotransformations implementing alcohol dehydrogenases (ADHs) are widespread, enzymes which...
Stereoselective reduction of prochiral ketones to the corresponding alcohols using biocatalysts has ...
The baker's yeast mediated biohydrogenation of unsaturated compounds containing a methylene group ma...
The baker's yeast biohydrogenation of the 2-substituted allyl alcohol 2a, in turn prepared from dihy...
Ethyl 4,4-dimethoxy-3-methylbut-2-enoate (1; R = CO2Et) has been prepared as a mixture of (E)-and (Z...
The baker’s yeast mediated reduction of 2-acetyl-3-methyl sulfolane 1 to provide the corresponding a...
(E)-2-methyl- and (E)-3-methyl-2,4-pentadien-1-ols are reduced to (S)-2-methyl- and (S)-3-methyl-4-p...
Reduction of a series of para-substituted 2-methyl-cinnamaldehy- des (1-7) at 20 °C and at pH = 2-3 ...
Microbial synthesis is an important contribution to Green Chemistry and production-integrated enviro...
This article summarizes our recent developments in allylic alcohol functionalization by the intercon...
α-Chiral amines are key intermediates for the synthesis of a plethora of chemical compounds at indus...
The stereoselective synthesis of (S)- and (R)-3-allyloxy-propane-1,2-diol has been accomplished in f...
Baker's yeast reduction of 1-(4-methoxyphenyl)propan-2-one, 4-phenylbutan-2-one, and 2-hydroxy-1-(4-...
This book is a collection of studies focused on the exploitation of enzyme stereoselectivity for the...
The microbial enantioselective reduction of C4-C8 methylketones to the corresponding (R)-alcohols wa...
Although biotransformations implementing alcohol dehydrogenases (ADHs) are widespread, enzymes which...
Stereoselective reduction of prochiral ketones to the corresponding alcohols using biocatalysts has ...
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