Reaction participants Show >> << Hide
- Name help_outline benzaldehyde Identifier CHEBI:17169 (CAS: 100-52-7) help_outline Charge 0 Formula C7H6O InChIKeyhelp_outline HUMNYLRZRPPJDN-UHFFFAOYSA-N SMILEShelp_outline O=Cc1ccccc1 2D coordinates Mol file for the small molecule Search links Involved in 14 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline hydrogen cyanide Identifier CHEBI:18407 (CAS: 74-90-8) help_outline Charge 0 Formula CHN InChIKeyhelp_outline LELOWRISYMNNSU-UHFFFAOYSA-N SMILEShelp_outline C#N 2D coordinates Mol file for the small molecule Search links Involved in 45 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline (S)-mandelonitrile Identifier CHEBI:36941 (Beilstein: 3588634,3588635) help_outline Charge 0 Formula C8H7NO InChIKeyhelp_outline NNICRUQPODTGRU-MRVPVSSYSA-N SMILEShelp_outline O[C@H](C#N)c1ccccc1 2D coordinates Mol file for the small molecule Search links Involved in 1 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
Cross-references
RHEA:77427 | RHEA:77428 | RHEA:77429 | RHEA:77430 | |
---|---|---|---|---|
Reaction direction help_outline | undefined | left-to-right | right-to-left | bidirectional |
UniProtKB help_outline |
|
Comments
Published in: Förster S., Roos J., Effenberger F., Wajant H. and Sprauer A. The first recombinant hydroxynitrile lyase and its application in the synthesis of (S)-cyanohydrins. Angew. Chem. Int. Ed. Engl. 35:437-439 (1996) DOI=10.1002/anie.199604371 Schmidt, M., Herve, S., Klempier, N. and Griengl, H. Preparation of optically active cyanohydrins using the (S)-hydroxynitrile lyase from Hevea brasiliensis. Tetrahedron 52 (1996) 7833–7840 DOI=10.1016/0040-4020(96)00354-7 Klempier N., Griengl H. Aliphatic (S)-cyanohydrins by enzyme catalyzed synthesis. Tetrahedron Lett. 34:4769-4772 (1993) DOI=10.1016/S0040-4039(00)74084-6