Search Substrates and Products (Substrate)

3.1.1.3

(R,S)-flurbiprofen ethyl ester + H2O

enantioselective reaction

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

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3.1.1.3

(R,S)-flurbiprofen ethyl ester + H2O

enantioselective hydrolysis, kinetic resolution, overview

(S)-flurbiprofen + ethanol

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3.1.1.3

(R,S)-flurbiprofen ethyl ester + H2O

high enantiomeric excess and conversion yield of 98% and 48%, respectively

(S)-flurbiprofen + ethanol

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3.1.1.3

(R,S)-flurbiprofen ethyl ester + H2O

enantioselective hydrolysis, kinetic resolution, overview

(S)-flurbiprofen + ethanol

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3.1.1.3

(R,S)-ibuprofen + 1-propanol

purified enzyme in a mixture of 1-propanol-isooctane in a ratio of 3:1, the conversion of racemic ibuprofen reaches 46% with very high enantioselectivity for production of the (S)-enantiomer

(S)-ibuprofen n-propyl ester + (R)-ibuprofen

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3.1.1.3

(R,S)-ibuprofen + 1-propanol

purified enzyme in a mixture of 1-propanol-isooctane in a ratio of 3:1, the conversion of racemic ibuprofen reaches 46% with very high enantioselectivity for production of the (S)-enantiomer

(S)-ibuprofen n-propyl ester + (R)-ibuprofen

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3.1.1.3

(R,S)-mandelonitrile + vinyl acetate

transesterification

(S)-cyano(phenyl)methyl acetate + (R)-mandelonitrite

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3.1.1.3

(R,S)-naproxen 2,2,2-trifluoroethyl thioester

(R,S)-profen 2,2,2-trifluoroethyl thioester

(S)-naproxen + 2,2,2-trifluorothioethanol + (R)-naproxen 2,2,2-trifluoroethyl thioester

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3.1.1.3

(R,S)-[4-[4a,6b(E)]]-6-[4,4-bis(4-fluorophenyl)-3-(1-methyl-1H-tetrazol-5-yl)-1,3-butadienyl]-tetrahydro-4-hydroxy-2H-pyran-2-one + isopropenyl acetate

(R)-(+)-[4-[4a,6b(E)]]-6-[4,4-bis(4-fluorophenyl)-3-(1-methyl-1H-tetrazol-5-yl)-1,3-butadienyl]-tetrahydro-4-hydroxy-2H-pyran-2-one + (S)-(-)-[4-[4a,6b(E)]]-6-[4,4-bis(4-fluorophenyl)-3-(1-methyl-1H-tetrazol-5-yl)-1,3-butadienyl]-tetrahydro-4-acetyloxy-2H-pyran-2-one + prop-1-en-2-ol

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3.1.1.3

(R/S)-ibuprofen methoxyethyl ester + H2O

(R)-ibuprofen methoxyethyl ester + (S)-ibuprofen + 2-methoxyethanol

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