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Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. 7. Synthesis of Two C27-C36 Units via Construction of the F Ring and Completely Stereoselective C-Glycosylation Using Mixed Lewis Acids.
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1997
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Bioorganic ChemistryEngineeringOrganic ChemistryChemistryPharmaceutical ChemistryMedicinal ChemistryF RingMarine SpongeC27-c36 UnitsBoron Trifluoride EtherateStereoselective SynthesisHalichondrin BAntimicrobial CompoundPharmacologyNatural Product SynthesisBiomolecular EngineeringNatural SciencesHalogenationSynthetic Chemistry
Two C27-C36 units of halichondrin B were synthesized starting from a C31-C34 alcohol, which was easily available from dimethyl L-tartrate, via construction of the F ring, methylation at the C31 position and C-glycosylation. These crucial reactions proceeded completely stereoselectively, and in particular the stereoselective C-glycosylation with allyltrimethylsilane took place only in the presence of both of two Lewis acids, boron trifluoride etherate and trimethylsilyl triflate.