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Literature summary for 4.1.2.47 extracted from

  • Avi, M.; Fechter, M.J.; Gruber, K.; Belaj, F.; Pöchlauer, P.; Griengl, H.
    Hydroxynitrile lyase catalysed synthesis of heterocyclic (R)- and (S)-cyanohydrins (2004), Tetrahedron, 60, 10411-10418.
No PubMed abstract available
Search for more literature for 4.1.2.47

Organism

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

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
HCN + 2-methyldihydrofuran analysis of diastereomeric distribution of the products, depending on different reaction conditions such as pH, reaction time, and solvent properties Hevea brasiliensis 3-hydroxy-2-methyltetrahydrofuran-3-carbonitrile
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 ?
HCN + 2-methyldihydrothiophen-3(2H)-one analysis of diastereomeric distribution of the products, depending on different reaction conditions such as pH, reaction time, and solvent properties Hevea brasiliensis 3-hydroxy-2-methyltetrahydrothiophen-3-carbonitrile
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 ?
HCN + tetrahydro-2H-3-pyranone
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 Hevea brasiliensis (3R)-3-hydroxytetrahydro-2H-pyran-3-carbonitrile enantiomeric excess at pH 4.75 is 48.3% ?
HCN + tetrahydro-3-furanone
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 Hevea brasiliensis (3R)-3-hydroxytetrahydrofuran-3-carbonitrile 81% enantiomeric excess ?