Macrocyclic Chiral Receptors toward Enantioselective Recognition of Naproxen
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文摘
A macrocyclic receptor based on a bischromenylurea and an ,'-(o,o'-dialkyl)diphenyl-p-xylylenediamine spacer provides a C2 chiral cavityto associate carboxylates by H-bonds. The extent of the selectivity obtained for the racemic receptor 2 and enantiomerically pure (S)-naproxenis 7.2:1. Steric repulsions close to the cavity are decisive for the chiral selectivity.

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