Global Deprotection

Remove the protecting groups from the original D-galactose to expose the remaining hydroxyl groups.

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Sterospecific Synthesis of (-)-Anisomycin from D-Galactose
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TOTAL SYNTHESIS OF D-(+)-SHOWDOMYCIN FROM SYN-2,5-DISUBSTITUTED TETRAHYDROFURAN
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Synthetic approach to kendomycin: Preparation of the C-glycosidic core
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Acid-promoted sequential cationic cyclizations for the synthesis of (±)-taiwaniaquinol B
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Characterization Stereoselective synthesis Chemical reactions Building blocks functional group interconversions Protecting groups Synthetic approach Isolation and Purification Retrosynthetic analysis Purification and characterization Introduction of chirality Final steps Stereochemistry Control Synthesis of Key Intermediates Formation of the Core Structure Bond Formation Choice of Starting Materials

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