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Total Synthesis of Trehalase Inhibitor, Trehazolin
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1993
Year
Medicinal ChemistryDiversity Oriented SynthesisBioorganic ChemistryDerivativesBiochemistryTrehalase InhibitorAbsolute ConfigurationNatural SciencesDiversity-oriented SynthesisMedicineTotal SynthesisStereoselective SynthesisPharmacologyPharmaceutical ChemistryInhibitory ActivityEnantioselective SynthesisDrug DiscoveryNatural Product Synthesis
Abstract The total synthesis of trehalase inhibitor, trehazolin has been accomplished by coupling the optically active aminocyclopentanepentaol with α-d-glucopyranosylisothiocyanate derivative, followed by subsequent oxazoline-ring formation and removal of the protecting groups, thereby confirming its absolute configuration.