If necessary, protect sensitive functional groups on the starting materials. Then, perform a series of chemical transformations to introduce or modify functional groups to build the carbon skeleton and desired stereochemistry. This may involve multiple reaction steps, such as reductions, oxidations, alkylations, and more.
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Nα-(benzyloxycarbonyl)-Nβ-(tert-butoxycarbonyl)-Nβ-methyl-L-α,β-diaminopropionic acid
(1R,2S,3R)-1-(t-butyldiphenylsilyloxy)-1-phenylbutane-2,3,4-triol
tert-Butyl-{(R)-2-[(3aR,5R,6S,6aR)-5-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yloxy]-1-phenyl-buta-2,3-dienyloxy}-diphenyl-silane
(R*,R*)-β-<(2-carboxyethyl)thio>-α-methoxy-2-(8-phenyloctyl)benzenepropanoic acid
methyl 4-methylene-6-(phenylthio)hexanoate
