An enantioselective NMR shift reagent for cationic aromatics |
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Authors: | Dignam Catherine F Richards Christopher J Zopf Jason J Wacker Lee S Wenzel Thomas J |
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Affiliation: | Department of Chemistry, Bates College, Lewiston, Maine 04240, USA. |
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Abstract: | [structure: see text] The water-soluble tetra l-prolinylmethyl derivative of a tetrasulfonated calix[4]resorcarene is an effective chiral NMR solvating agent for compounds with bicyclic aromatic or indole rings. Complexation of bicyclic substrates with the calix[4]resorcarene is likely promoted by hydrophobic effects. The bicyclic substrates have larger association constants with the calix[4]resorcarene than similar phenyl-containing compounds. Substantial enantiomeric discrimination is observed for several resonances in the (1)H NMR spectra of these substrates. |
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