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Literature summary extracted from

  • Klempier, N.; Griengl, H.
    Alphatic (S)-cyanohydrins by enzyme catalyzed synthesis (1993), Tetrahedron Lett., 34, 4769-4772.
No PubMed abstract available

Organism

EC Number Organism UniProt Comment Textmining
4.1.2.47 Hevea brasiliensis P52704
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-

Source Tissue

EC Number Source Tissue Comment Organism Textmining
4.1.2.47 leaf
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Hevea brasiliensis
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Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
4.1.2.47 cyanide + 2,2-dimethylpropanal
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Hevea brasiliensis (2S)-2-hydroxy-3,3-dimethylbutanenitrile 67% enantiomeric excess ?
4.1.2.47 cyanide + 2-methylpropanal
-
Hevea brasiliensis (2S)-2-hydroxy-3-methylbutanenitrile 81% enantiomeric excess ?
4.1.2.47 cyanide + 3-phenoxybenzaldehyde
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Hevea brasiliensis (2S)-hydroxy(3-phenoxyphenyl)acetonitrile 20% enantiomeric excess ?
4.1.2.47 cyanide + benzaldehyde
-
Hevea brasiliensis (S)-mandelonitrile 94% enantiomeric excess ?
4.1.2.47 cyanide + butanal
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Hevea brasiliensis (2S)-2-hydroxypentanenitrile 80% enantiomeric excess ?
4.1.2.47 cyanide + hexanal
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Hevea brasiliensis 2-hydroxyheptanenitrile 84% enantiomeric excess ?
4.1.2.47 cyanide + nonanal
-
Hevea brasiliensis 2-hydroxydecanenitrile 85% enantiomeric excess ?
4.1.2.47 cyanide + prop-2-enal
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Hevea brasiliensis 2-hydroxybut-3-enenitrile 84% enantiomeric excess ?