4.1.2.38: benzoin aldolase
This is an abbreviated version!
For detailed information about benzoin aldolase, go to the full flat file.
Word Map on EC 4.1.2.38
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4.1.2.38
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thiamin
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bal
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carboligation
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fluorescens
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benzoylformate
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thdp-dependent
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r-benzoin
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stereoselective
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enantioselective
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diphosphate-dependent
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biovar
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acyloins
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biocatalysis
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model-based
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carbon-carbon
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synthesis
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carboligase
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1',4'-iminopyrimidine
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propanal
- 4.1.2.38
- thiamin
- bal
-
carboligation
- fluorescens
- benzoylformate
-
thdp-dependent
-
r-benzoin
-
stereoselective
-
enantioselective
-
diphosphate-dependent
-
biovar
- acyloins
-
biocatalysis
-
model-based
-
carbon-carbon
- synthesis
-
carboligase
-
1',4'-iminopyrimidine
- propanal
Reaction
Synonyms
BAL, benzaldehyde lyase, benzoin aldolase, BZL, BznB, lyase, benzaldehyde
ECTree
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Application
Application on EC 4.1.2.38 - benzoin aldolase
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synthesis
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application of benzaldehyde lyase as a heterogeneous catalyst in the continuous synthesis (in a packed bed in a continously operated plug flow reactor for over 140 h) of the chiral 2-hydroxy ketone (R)-2-hydroxy-1-phenyl-propanone
synthesis
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stereoselective synthesis of novel benzoins catalysed by benzaldehyde lyase in a gel-stabilised two-phase system. (R)-1,2-di(3-furanyl)-2-hydroxyethanone, (R)-2-hydroxy-1,2-di(3-thienyl) ethanone, (R)-1,2-di(4-ethoxyphenyl)-2-hydroxyethanone, (R)-1,2-di(3-ethoxyphenyl)-2-hydroxyethanone, (R)-2-hydroxy-1,2-di(3-tolyl)ethanone, and (R)-1,2-di(benzofuran-2-yl)-2-hydroxyethanone are prepared with yields up to 31.8% and enantiomeric excess of more than 99%
synthesis
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the enzyme is a tool in chemoenzymatic synthesis of chiral alpha-hydroxyketones
synthesis
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(R)-benzoin is synthesized from benzaldehyde using the most stable variant immobilized in packed-bed reactors via the SpyCatcher/SpyTag system. Over a period of seven days, (R)-benzoin is produced with a stable spacetime-yield of 9.3 mmol/l and day
synthesis
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(R)-benzoin is synthesized from benzaldehyde using the most stable variant immobilized in packed-bed reactors via the SpyCatcher/SpyTag system. Over a period of seven days, (R)-benzoin is produced with a stable spacetime-yield of 9.3 mmol/l and day
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synthesis
-
application of benzaldehyde lyase as a heterogeneous catalyst in the continuous synthesis (in a packed bed in a continously operated plug flow reactor for over 140 h) of the chiral 2-hydroxy ketone (R)-2-hydroxy-1-phenyl-propanone
-