The next step is to separate the racemic mixture into its individual enantiomers (R and S). One common method for this is to use chiral resolution techniques. For example, you can react the racemic mixture with a resolving agent or perform fractional crystallization using a chiral resolving agent.
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(S)-1-benzyloxy-4-(2,5-dimethoxy-3,4,6-trimethylphenyl)-2-methyl-butan-2-ol
(4S,5S)-5-Fluoromethyl-5-((S)-toluene-4-sulfinylmethyl)-4,5-dihydro-oxazole-4-carboxylic acid methyl ester
