首页> 外文期刊>Journal of Inclusion Phenomena and Macrocyclic Chemistry >Synthesis of Novel Chiral C_2-symmetric Diaza-18-crown-6 Ether Derivatives and Their Enantioselective Recognition of Amino Acid Derivatives
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Synthesis of Novel Chiral C_2-symmetric Diaza-18-crown-6 Ether Derivatives and Their Enantioselective Recognition of Amino Acid Derivatives

机译:新型手性C_2对称Diaza-18-crown-6醚衍生物的合成及其对氨基酸衍生物的对映选择性识别

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摘要

New chiral diaza-18-crown-6 ether derivatives,5 and 6 were synthesized from(R)-(-)-2-amino-1-butanol.These chiral artificial receptors exhibit pronounced chiral recognition toward the enantiomers of L-and D-amino acid derivatives.The highest enantioselectivity was observed in the case of Trp-OMe centre dot HCl(K_D/K_L= 12.5).
机译:从(R)-(-)-2-氨基-1-丁醇合成了新的手性diaza-18-crown-6醚衍生物5和6。这些手性人工受体对L-和D的对映体表现出明显的手性识​​别能力。在Trp-OMe中心点HCl(K_D / K_L = 12.5)的情况下,对映体选择性最高。

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