The activated substrate undergoes an enantioselective transformation, which, in the case of enantioselective cyanohydrin synthesis, typically involves the addition of a cyanide source to the substrate. The chiral environment created by the peptide-metal complex directs the addition of the cyanide ion to one face of the substrate, resulting in the formation of the desired enantiomer.
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N-((2-hydroxy-1-naphthyl)methylene)-(S)-valyl-(S)-phenylalanine
Cyclopropanecarboxylic acid, 1-amino-2-ethenyl-, (1R,2S)- (9CI)
2H-Pyran-4-ol, tetrahydro-4-methyl-2-propyl-, acetate
