首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >One-pot synthesis of enantiopure syn-1,3-diacetates from racemic syn/anti mixtures of 1,3-diols by dynamic kinetic asymmetric transformation
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One-pot synthesis of enantiopure syn-1,3-diacetates from racemic syn/anti mixtures of 1,3-diols by dynamic kinetic asymmetric transformation

机译:通过动态动力学不对称转化从1,3-二醇的外消旋式正/反混合物一锅合成对映体纯-1,3-二乙酸酯

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摘要

A one-pot synthesis of enantiomerically pure syn-1,3-diacetates starting from readily accessible racemic diastereomeric mixtures of 1,3-diols has been realized by combining (i) enzymatic transesterification, (h) ruthenium-catalyzed epimerization of a secondary alcohol in a diol or diol monoacetate, and (iii) intramolecular acyl migration in a syn-1,3-diol monoacetate. The in situ coupling of these three processes results in an efficient enantioselective synthesis of acyclic syn-1,3-diacetates via combined deracemization/deepimerization and constitutes a dynamic kinetic asymmetric transformation concept. Several differently substituted unsymmetrical, acyclic syn-1,3-diacetates were obtained in yields up to 73% with excellent enantioselectivities (>99%) and good diastereomeric ratios (>90% syn).
机译:通过结合(i)酶促酯交换反应,(h)钌催化的仲醇差向异构化反应,可以轻松地从1,3-二醇的外消旋非对映异构体混合物开始对映体纯的syn-1,3-diacetate的一锅合成。在二醇或二醇单乙酸酯中,和(iii)在合成的1,3-二醇单乙酸酯中的分子内酰基迁移。这三个过程的原位偶合导致无环合成的1,3-双乙酸酯通过脱氮/加深二茂合物的有效对映选择性合成,并构成了动态动力学不对称转化概念。获得了几种不同取代的不对称非环状无环1,3-二乙酸酯,收率高达73%,具有出色的对映选择性(> 99%)和良好的非对映体比率(> 90%syn)。

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