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首页> 外文期刊>Journal of Organometallic Chemistry >Determination of absolute configurations of amino acids by asymmetric autocatalysis of 2-alkynylpyrimidyl alkanol as a chiral sensor
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Determination of absolute configurations of amino acids by asymmetric autocatalysis of 2-alkynylpyrimidyl alkanol as a chiral sensor

机译:通过2-炔基嘧啶链烷醇作为手性传感器的不对称自催化测定氨基酸的绝对构型

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摘要

Asymmetric autocatalysis of 2-alkynyl-5-pyrimidyl alkanol is employed as a chiral sensor of 20 amino acids. Asymmetric autocatalysis using amino acids as chiral initiators gave pyrimidyl alkanols of the absolute configurations that were correlated with those of the amino acids. The enantiomeric excesses of pyrimidyl alkanol are invariably high even when the enantiomeric excess of amino acids is as low as 0.1%. Thus, by determining the absolute configuration of pyrimidyl alkanol with high enantiomeric excess, one can determine the absolute configuration of amino acids even when their enantiomeric excess is low. (c) 2006 Elsevier B.V. All rights reserved.
机译:2-炔基-5-嘧啶链烷醇的不对称自催化被用作20个氨基酸的手性传感器。使用氨基酸作为手性引发剂的不对称自催化反应得到的嘧啶基链烷醇的绝对构型与氨基酸的构型相关。即使当氨基酸的对映体过量低至0.1%时,嘧啶基链烷醇的对映体过量也总是高的。因此,通过确定具有高对映体过量的嘧啶基链烷醇的绝对构型,即使当其对映体过量低时,也可以确定氨基酸的绝对构型。 (c)2006 Elsevier B.V.保留所有权利。

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