Reaction participants Show >> << Hide
- Name help_outline 4-methoxybenzaldehyde Identifier CHEBI:28235 (CAS: 123-11-5) help_outline Charge 0 Formula C8H8O2 InChIKeyhelp_outline ZRSNZINYAWTAHE-UHFFFAOYSA-N SMILEShelp_outline C=1(C=CC(C(=O)[H])=CC1)OC 2D coordinates Mol file for the small molecule Search links Involved in 2 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 (2S)-2-hydroxy-2-(4-methoxyphenyl)acetonitrile Identifier CHEBI:197328 Charge 0 Formula C9H9NO2 InChIKeyhelp_outline WLDAAMXETLHTER-SECBINFHSA-N SMILEShelp_outline C=1C=C([C@@H](C#N)O)C=CC1OC 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:77447 | RHEA:77448 | RHEA:77449 | RHEA:77450 | |
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Reaction direction help_outline | undefined | left-to-right | right-to-left | bidirectional |
UniProtKB help_outline |
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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