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Diastereo- and enantio-selective binding of octyl glucosides by an artificial receptor
63
Citations
11
References
1992
Year
Bioorganic ChemistryOrganic ChemistryChemistryChemical BiologySpectra-structure CorrelationOctyl GlucosidesStructure ElucidationStereoselective SynthesisEnantio-selective BindingChemical MeasurementTetrahydroxycholaphane 1ABiochemistryG Protein-coupled ReceptorReceptor (Biochemistry)Mechanism Of ActionNon-peptide LigandPharmacologyEnantioselective SynthesisAssociation ConstantsOctyl Glucosides 2-5Artificial ReceptorNatural SciencesFunctional SelectivityMedicineDrug Discovery
1 H NMR titration experiments have been used to measure the association constants between tetrahydroxycholaphane 1a and the octyl glucosides 2-5; the cholaphane has been shown to discriminate quite effectively between the stereoisomers, showing a diastereoselectivity of ca. 5.5:1 in respect of 2 and 3, and an enantioselectivity of ca. 3:1 in respect of 3 and 5.
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