DKR is a powerful strategy for achieving asymmetric synthesis. It involves the selective conversion of one enantiomer of a racemic substrate into a product, leaving the other enantiomer unchanged. In the context of spiro compounds, this can be useful for obtaining the desired enantiomer with high selectivity.
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(3R,7aS)-3-phenyl-7a-(3-phenylpropyl)-2,3,7,7a-tetrahydropyrrolo[2,1-b]oxazol-5-one
(R)-(+)-1-phenyl-3-((3-fluoro-4-phenyl)phenyl)-1-butene
dimethyl-(2-methyl-3-phenyl-propyl)-amine
(2S,3S)-2-AMINO-3-HYDROXY-4-METHYL-PENTANOIC ACID
(1R)-acetic acid 1-methyl-3-phenylprop-2-ynyl ester
Butanoic acid, 2-[(benzoylamino)methyl]-3-hydroxy-, methyl ester, (2R,3S)-
