Literature summary for 4.1.2.47 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

Search for more literature for 4.1.2.47

Activating Compound

Activating Compound	Comment	Organism	Structure
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

Organism	UniProt	Comment	Textmining
Hevea brasiliensis	-	-	-

Substrates and Products (Substrate)

Substrates	Comment Substrates	Organism	Products	Comment (Products)	Rev.	Reac.
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	-	?
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	-	?
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	-	?
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	-	?

Use of this online version of BRENDA is free under the CC BY 4.0 license. See terms of use for full details.

Release 2023.1 (January 2023)