Activating Compound | Comment | Organism | Structure |
---|---|---|---|
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 |
Organism | UniProt | Comment | Textmining |
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Prunus dulcis | - |
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Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
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 | - |
? | |
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 | - |
? | |
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 | - |
? | |
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 | - |
? |