Reaction participants Show >> << Hide
- Name help_outline formylthiophene Identifier CHEBI:87301 (CAS: 98-03-3) help_outline Charge 0 Formula C5H4OS InChIKeyhelp_outline CNUDBTRUORMMPA-UHFFFAOYSA-N SMILEShelp_outline O=Cc1cccs1 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
- 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 (2R)-2-hydroxy-2-(thiophen-2-yl)acetonitrile Identifier CHEBI:197332 Charge 0 Formula C6H5NOS InChIKeyhelp_outline MDOLBFYWOIYESI-RXMQYKEDSA-N SMILEShelp_outline C=1C=CSC1[C@H](O)C#N 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:77455 | RHEA:77456 | RHEA:77457 | RHEA:77458 | |
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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