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• W2952523360 endingPage "1294" @default.
• W2952523360 startingPage "1289" @default.
• W2952523360 abstract "Novel <TEX>$H_8$</TEX>-binaphthol-based chiral receptors appended with an uryl moiety (2a) and a guanidinium moiety (2b) have been designed and synthesized for the enantioselective recognition of 1,2-amino alcohols via reversible imine formation. The selectivities (<TEX>$K_R/K_S$</TEX> = 9.8 ~ 19.4) of 2b in imine formation with 1,2-amino alcohols are higher than those of 2a (<TEX>$K_R/K_S$</TEX> = 1.8 ~ 4.5). Similar efficiency trend have been observed in the conversion of L-amino acids to D-amino acids, i.e., the efficiency of the receptor 2b (D/L ratio: 4.3 ~ 10.1) is superior to 2a (D/L ratio: 4.0 ~ 8.7)." @default.
• W2952523360 created "2019-06-27" @default.
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• W2952523360 date "2010-05-20" @default.
• W2952523360 modified "2023-10-15" @default.
• W2952523360 title "Synthesis of Novel H₈-Binaphthol-based Chiral Receptors and Their Applications in Enantioselective Recognition of 1,2-Amino alcohols and Chirality Conversion of L-Amino acids to D-Amino acids" @default.
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• W2952523360 doi "https://doi.org/10.5012/bkcs.2010.31.5.1289" @default.
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