Search Substrates and Products (Substrate)

3.1.1.3

(+-)-2-hydroxy-4-phenylbutyric acid ethyl ester + H2O

enantioselectivity of the immobilized enzyme in this reaction is increased 40fold by presence of 0.1% CTAB

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3.1.1.3

(+/-)-trans-3-(4'-methoxy-phenyl)-glycidyl methyl ester + H2O

50% conversion yield after 4 h in 100 mM potassium phosphate buffer, pH 7.5, at 30 °C

(2R,3S)-3-(4-hydroxyphenyl)oxirane-2-carboxylic acid + methyl (2S,3R)-3-(4-hydroxyphenyl)oxirane-2-carboxylate + methanol

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3.1.1.3

(3aR,6aS)-2-oxo-3,3a,4,6a-tetrahydro-2H-cyclopenta[b]furan-3-yl acetate + H2O

(3S,3aR,6aS)-2-oxo-3,3a,4,6a-tetrahydro-2H-cyclopenta[b]furan-3-yl acetate + (3R,3aS,6aS)-3-hydroxy-3,3a,4,6a-tetrahydro-2H-cyclopenta[b]furan-2-one + acetate

3.1.1.3

(4S)-4-tert-butyl-2-phenyl-1,3-oxazol-5(4H)-one + butanol

butyl (2S)-2-(benzoylamino)3,3-dimethylbutanoate

3.1.1.3

(5R,6R)-6-hydroxy-5,6-dihydro-1,10-phenanthrolin-5-yl acetate + vinyl acetate

(5S,6S)-6-hydroxy-5,6-dihydro-1,10-phenanthrolin-5-yl acetate + (5R,6R)-5,6-dihydro-1,10-phenanthroline-5,6-diyl diacetate + ethenol

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3.1.1.3

(R)-2-ethylhexanoic acid ethyl ester + H2O

(R)-2-ethylhexanoate + ethanol

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3.1.1.3

(R)-3,5,5-trimethylhexanoic acid ethyl ester + H2O

(R)-3,5,5-trimethylhexanoate + ethanol

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3.1.1.3

(R,S)-1-phenylethylamine + ethyl methoxyacetate

(S)-1-phenylethylamine + 2-methoxy-N-[(1R)-1-phenylethyl]acetamide + ethanol

3.1.1.3

(R,S)-2-O-butyryl-2-phenylacetate + H2O

Enantioselectivity of the reaction can be obtained with various methods of enzyme immoblisation and reaction conditions

(R)-2-O-butyryl-2-phenylacetate + (2S)-hydroxy(phenyl)ethanoic acid + butyrate

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3.1.1.3

(R,S)-flurbiprofen ethyl ester + H2O

enantioselective reaction

(S)-flurbiprofen ethyl ester + (R)-flurbiprofen + ethanol

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