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Stereoselective Synthesis of the S- and Y-Ring Systems Of Maitotoxin.
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1996
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EngineeringHeterocyclicBiochemistryNatural SciencesDiversity-oriented SynthesisOrganic ChemistryY-ring SystemsSeven-membered S-Stereoselective SynthesisHeterocycle ChemistryRearrangement-ring ExpansionNatural Product SynthesisSynthetic ChemistryBiomolecular Engineering
The seven-membered S- and Y-ring systems of maitotoxin (1) were stereoselectively synthesized based on the rearrangement-ring expansion of the six-membered ethers having the mesylate group on the α-side chain.