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Literature summary for 4.1.2.47 extracted from

  • Schmidt, M.; Herve, S.; KLempier, N.; Griengl, H.
    Preparation of optically active cyanohydrins using the (S)-hydroxynitrile lyase from Hevea brasiliensis (1996), Tetrahedron, 52, 7833-7840.
No PubMed abstract available
Search for more literature for 4.1.2.47

Organism

Organism UniProt Comment Textmining
Hevea brasiliensis P52704 recombinant
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
cyanide + 2-methoxybenzaldehyde
-
 Hevea brasiliensis (2S)-2-hydroxy-2-(2-methoxyphenyl)acetonitrile 77% enantiomeric excess ?
cyanide + 3-methoxybenzaldehyde
-
 Hevea brasiliensis (2S)-2-hydroxy-2-(3-methoxyphenyl)acetonitrile 99% enantiomeric excess ?
cyanide + 3-phenoxybenzaldehyde
-
 Hevea brasiliensis (2S)-2-hydroxy-2-(3-phenoxyphenyl)acetonitrile 99% enantiomeric excess ?
cyanide + 3-phenylpropanal
-
 Hevea brasiliensis (2S)-2-hydroxy-4-phenylbutanenitrile 93% enantiomeric excess ?
cyanide + 4-methoxybenzaldehyde
-
 Hevea brasiliensis (2S)-2-hydroxy-2-(4-methoxyphenyl)acetonitrile 95% enantiomeric excess ?
cyanide + benzaldehyde
-
 Hevea brasiliensis (2S)-2-hydroxy-2-phenylacetonitrile i.e. (S)-mandelonitrile, more than 99% enantiomeric excess ?
cyanide + cinnamaldehyde
-
 Hevea brasiliensis (2S)-2-hydroxy-4-phenyl-(E)-but-3-enenitrile 95% enantiomeric excess ?
cyanide + cyclohex-3-ene-1-carbaldehyde
-
 Hevea brasiliensis (2S)-2-(cyclohex-3-enyl)-2-hydroxyacetonitrile 99% enantiomeric excess ?
cyanide + cyclohexanecarbaldehyde
-
 Hevea brasiliensis (2S)-2-cyclohexyl-2-hydroxyacetonitrile 99% enantiomeric excess ?
cyanide + phenylacetaldehyde
-
 Hevea brasiliensis (2S)-2-hydroxy-3-phenylpropanenitrile 99% enantiomeric excess ?

Synonyms

Synonyms Comment Organism
(S)-Hydroxynitrile lyase
-
 Hevea brasiliensis