首页> 外文期刊>Chemistry: A European journal >Highly efficient synthesis of enantiopure diacetylated C-2-symmetric diols by ruthenium- and enzyme-catalyzed dynamic kinetic asymmetric transformation (DYKAT)
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Highly efficient synthesis of enantiopure diacetylated C-2-symmetric diols by ruthenium- and enzyme-catalyzed dynamic kinetic asymmetric transformation (DYKAT)

机译:通过钌和酶催化的动态动力学不对称转化(DYKAT)高效合成对映体纯的二乙酰化C-2-对称二醇

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摘要

Highly efficient synthesis of enantiopure diacetates of 2,4-pentanediol and 2,5-hexanediol starting from commercially available mixtures of the diols (dl/meso approximate to 1:1) has been realized by combining a fast ruthenium-catalyzed epimerization with an enzymatic transesterification. The in situ coupling of these two processes produces the diacetates in high yield in > 99% enantiomeric excess.
机译:通过将快速钌催化的差向异构化与酶促反应相结合,已经从二醇的市售混合物(dl / meso近似于1:1)开始高效合成2,4-戊二醇和2,5-己二醇的对映体纯二乙酸酯。酯交换。这两个过程的原位偶联以高收率产生> 99%对映体过量的二乙酸酯。

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