Organic & Biomolecular Chemistry · 2009 · 52 citations · 19 references
PharmacyChemistryMedicinal ChemistryNatural Product BiosynthesisOrganic ChemistrySynthetic Medicinal ChemistryNatural Product DerivatizationSolvent-free SynthesisBenzyl Group RemovalFlavonoid GlycosidesFlavonoid GlycosylationGlycoside Natural ProductsGlycosylation Of Natural ProductsMild Reaction ConditionsNatural Product GlycosylationNatural Product Total Synthesis
An efficient selective demethylation and debenzylation method for aryl methyl/benzyl ethers using magnesium iodide under solvent-free conditions has been developed and applied to the synthesis of natural flavone and biphenyl glycosides. A variety of functional groups including glycoside were tolerated under the reaction conditions. Experimental results indicated that the removal of an O-benzyl group was easier than that of an O-methyl group, regardless of wherever they were meta or para to the carbonyl. Thus selective debenzylation can be achieved for substrates bearing both benzyloxy and methoxy groups.
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Recent advances in ether dealkylation
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Kv1.3-Blocking 5-Phenylalkoxypsoralens: A New Class of Immunomodulators
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