Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary extracted from

  • Gaisberger, R.P.; Fechter, M.H.; Griengl, H.
    The first hydroxynitrile lyase catalysed cyanohydrin formation in ionic liquids (2004), Tetrahedron, 15, 2959-2963.
No PubMed abstract available

Activating Compound

EC Number Activating Compound Comment Organism Structure
4.1.2.10 additional information reaction in a two phase solvent system aqueous buffer and ionic liquid. When compared to the use of organic solvents as the nonaqueous phase, the reaction rate is significantly increased whereas the enantioselectivity remained good Prunus dulcis
4.1.2.47 additional information reaction in a two phase solvent system aqueous buffer and ionic liquid. Compared to the use of organic solvents as the nonaqueous phase, the reaction rate is significantly increased whereas the enantioselectivity remained good Hevea brasiliensis

Organism

EC Number Organism UniProt Comment Textmining
4.1.2.10 Prunus dulcis
-
-
-
4.1.2.47 Hevea brasiliensis
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
4.1.2.10 HCN + benzaldehyde reaction in a two phase solvent system aqueous buffer and ionic liquid. When compared to the use of organic solvents as the nonaqueous phase, the reaction rate is significantly increased whereas the enantioselectivity remains good Prunus dulcis (R)-mandelonitrile
-
 ?
4.1.2.10 HCN + decanal reaction in a two phase solvent system aqueous buffer and ionic liquid. When compared to the use of organic solvents as the nonaqueous phase, the reaction rate is significantly increased whereas the enantioselectivity remains good Prunus dulcis (R)-2-hydroxyundecanenitrile
-
 ?
4.1.2.10 HCN + dodecanal reaction in a two phase solvent system aqueous buffer and ionic liquid. When compared to the use of organic solvents as the nonaqueous phase, the reaction rate is significantly increased whereas the enantioselectivity remains good Prunus dulcis (R)-2-hydroxytridecanenitrile
-
 ?
4.1.2.10 HCN + undecanal reaction in a two phase solvent system aqueous buffer and ionic liquid. When compared to the use of organic solvents as the nonaqueous phase, the reaction rate is significantly increased whereas the enantioselectivity remains good Prunus dulcis (R)-2-hydroxydodecanenitrile
-
 ?
4.1.2.47 HCN + benzaldehyde reaction in a two phase solvent system aqueous buffer and ionic liquid. Compared to the use of organic solvents as the nonaqueous phase, the reaction rate is significantly increased whereas the enantioselectivity remains good Hevea brasiliensis (S)-mandelonitrile
-
 ?
4.1.2.47 HCN + decanal reaction in a two phase solvent system aqueous buffer and ionic liquid. Compared to the use of organic solvents as the nonaqueous phase, the reaction rate is significantly increased whereas the enantioselectivity remains good Hevea brasiliensis (S)-2-hydroxyundecanenitrile
-
 ?
4.1.2.47 HCN + dodecanal reaction in a two phase solvent system aqueous buffer and ionic liquid. Compared to the use of organic solvents as the nonaqueous phase, the reaction rate is significantly increased whereas the enantioselectivity remains good Hevea brasiliensis (S)-2-hydroxytridecanenitrile
-
 ?
4.1.2.47 HCN + undecanal reaction in a two phase solvent system aqueous buffer and ionic liquid. Compared to the use of organic solvents as the nonaqueous phase, the reaction rate is significantly increased whereas the enantioselectivity remains good Hevea brasiliensis (S)-2-hydroxydodecanenitrile
-
 ?