Journal
CHEMICAL COMMUNICATIONS
Volume 48, Issue 40, Pages 4881-4883Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c2cc31127e
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Funding
- Grants-in-Aid for Scientific Research [10J01768] Funding Source: KAKEN
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Enantioselective recognition of amino acids was achieved by using a highly ordered chiral assembly of achiral porphyrin on a chiral molecular gel. Exceptionally high enantioselectivity was observed for histidine derivatives by monitoring the CD patterns and fluorescence quenching, K-SV (L): 26.3 x 10(3) M-1; K-SV (D)-enantiomer: 7.03 x 10(3) M-1.
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